LBIS® 小鼠 C-肽 ELISA 试剂盒(U型) LBIS® C-Peptide-Mouse (U type)

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® C-Peptide-Mouse (U type)LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type)

LBIS® 小鼠 C-肽 ELISA 试剂盒(U 型)

  胰岛素是细胞中的单链胰岛素原合成后,形成二硫键,通过酶分解激活,裂解成肽与胰岛素。小鼠、大鼠的胰岛素的氨基酸序列相同,但肽部分稍有不同。小鼠C肽1是 29 个氨基酸,2是 31 个的单链肽。肽是从胰岛素原分离后,与胰岛素一同分泌生成的。长期以来,人们一直认为肽没有生物活性,仅在合成胰岛素过程中,保证A链和B链正确折叠以及二硫键正确配对时起作用。近年,随着研究的不断深入,证明了肽具有多种生物学作用。首先,10-9M 的肽能与内皮细胞、肾小管上皮细胞和成纤维细胞表面的G蛋白偶联受体结合。激活细胞中钙离子依赖性的信号、激活 Na-K-ATPase、促进内皮细胞的 NO 合成、与受体的结合有立体结构特异性;与胰岛素、胰岛素原、IGF-I、-II、NPY 之间无交叉反应。而且通过对缺少肽的Ⅰ型糖尿病患者注射肽类药物,能起到增强骨骼肌以及皮肤的血液循环、降低肾小球超滤的风险、抑制白蛋白从尿液中的排泄、改善神经机能的作用。但对身体健康的人来说,这类药物没有此等功效。因此,建议Ⅰ型糖尿病患者可以在注射胰岛素的同时,投放肽,有利于防止并发症的发生。

  肽的末端的五肽(27-31)在与受体的结合中起着重要的作用,缺少这部分的 Des(27-31)肽就会失去它的作用。这种五肽可以完全取代肽和受体的结合,激活 Na+-K+ATPase。有报告指出新生大鼠中 Des(27-31)肽的存在量约占肽总量的37%,而在成年大鼠中只占8.5%。

  肽在血液中的寿命是胰岛素的好几倍。在临床上,可以通过测量肽在血液中的浓度来观察胰岛素的合成和分泌功能。且肽在尿液中多量排除,一定程度上与血液中肽的平均值相关,所以也可以通过尿液来检测。

  作为人工胰岛中胰岛素分泌的指标,肽测量是有效的。由于在培养液中经常添加胰岛素,如果要测量培养后培养液中的胰岛素的话,就不能很好地区别出分泌的胰岛素和添加的胰岛素,必须减掉培养开始时胰岛素的量。这种情况下,如果分泌的胰岛素量过少,测量误差的影响会增大,从而不能做出正确的判断。这时候,如果测量肽,因为肽与胰岛素是等摩尔分泌的,所以能够正确判断分泌的胰岛素。

  本公司的整套产品能够识别肽1、2的交叉部分,可以测量肽的总量。

◆特点

● 短时间测定(完全反应时间:5小时)

● (标准用量 10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定密度和高再现性

◆构成

组成

状态

容量

(A) 抗体固相化   96 孔板

洗净后使用

96 wells(8×12)/1 块

(B) 标准溶液(6,000 pg/mL)

稀释后使用

500 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 抗C-肽抗体生物素结合

稀释后使用

100 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

100 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应停止液(1M   H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

4 张

使用说明书

1 份

◆样本

小鼠的血清或血浆

10 μL/well(用本品配备的缓冲液稀释后、50 μ分注在孔板中。)

◆测定范围

46.9~3,000 pg/mL(标准曲线范围)

234.5~15,000 pg/mL(检体量 10 μL 的时候)

◆Validation data

 

精度测试(检测内变异系数)

 

样本

A

B

1

976

238

2

969

230

3

965

230

4

1023

235

5

977

231

6

1018

228

7

1038

229

8

995

225

mean

995

231

SD

27.7

4.10

CV(%)

2.78

1.78

单位:pg/mL

再现性测试(检测内变异系数)

 

测量日/检体

C

D

E

第0天

1502

301

60.9

第1天

1500

302

63.8

第2天

1499

301

62.2

第3天

1501

300

58.8

mean

1500

301

61.4

SD

1.12

0.66

2.13

CV(%)

0.07

0.22

3.46

单位:pg/mL, n=4

添加回收测试

 

样本F

添加量

实测值

回收量

回收率(%)

0.00

300

265

551

250

94

398

683

382

96

531

827

527

99

单位:pg/mL, n=2

样本G

添加量

实测值

回收量

回收率(%)

0.00

58.2

28.9

86.7

28.5

99

38.6

98.2

40.0

104

77.4

139

80.8

104

单位:pg/mL, n=2

稀释直线性测试

用稀释缓冲液分三次连续稀释2个血清检体的结果,直线回归方程的 R是 1.00 。

欲了解更多相关产品信息,请点击文字:LBIS® 疾病相关动物模型ELISA试剂盒系列


相关资料


LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type) LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type) LBIS® 小鼠 C-肽 ELISA 试剂盒(U型)                              LBIS® C-Peptide-Mouse (U type)
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献


 1.

Inhibition of Gastric Inhibitory Polypeptide Receptor Signaling in Adipose Tissue Reduces Insulin Resistance and Hepatic Steatosis in High-Fat Diet-Fed Mice. Joo E, Harada N, Yamane S, Fukushima T, Taura D, Iwasaki K, Sankoda A, Shibue K, Harada T, Suzuki K, Hamasaki A, Inagaki N. Diabetes. 2017 Apr;66(4):868-879.


 2.

Inhibition of Gastric Inhibitory Polypeptide Receptor Signaling in Adipose Tissue Reduces Insulin

Resistance and Hepatic Steatosis in High Fat Diet-Fed Mice. Joo E, Harada N, Yamane S, Fukushima

T, Taura D, Iwasaki K, Sankoda A, Shibue K, Harada T, Suzuki K, Hamasaki A, Inagaki N. Diabetes.

2017 Jan 17.


 3.

Insulin Release from the Beta Cells in Acatalasemic Mice Is Highly Susceptible to Alloxan-Induced Oxidative Stress. Kazunori Takemoto, Wakana Doi, Ken Kataoka, Kohji Ishihara, Da-Hong Wang, Hitoshi Sugiyama, Noriyoshi Masuoka. Journal of Diabetes Mellitus, 2015, 5, 81-89


 4.

Effect of Burdock Root and the Fermented Product on Alloxan-Induced Mouse Hyperglycemia

Wakana Doi, Yumi Asada, Ayaka Ohno, Yoshiko Okuda, Shota Masuda, Ayano Matsumoto,

Chihiro Mori, Takaya Agarie, Kohji Ishihara, Takayuki Murakami & Noriyoshi Masuoka Journal of

Food Research; Vol. 4, No. 4; 201


 5.

Tissue Complex of Adult Pancreatic Duct and Vascular Endothelial Cells Promotes In Vitro Differentiation into Insulin-Producing Cells. Jun Kanamune, Chongmun Kim, Yasuhiro Iwanaga, Jorge David Rivas-Carrillo, Shoichiro Sumi, Shinji Uemoto and Kazuyuki Yokokawa. J Stem Cell Res Dev 2015, 2: 005


 6.

Anti-diabetic effect of purple corn extract on C57BL/KsJ db/db mice. Bo Huang, Zhiqiang Wang, Jong Hyuk Park, Ok Hyun Ryu, Moon Ki Choi, Jae-Yong Lee, Young-Hee Kang, and Soon Sung Lim. Nutr Res Pract. 2015 Feb;9(1):22-29.


 7.

Xanthohumol Improves Diet-induced Obesity and Fatty Liver by Suppressing Sterol Regulatory Element-binding Protein (SREBP) Activation. Miyata S, Inoue J, Shimizu M, Sato R. J Biol Chem. 2015 Aug 14;290(33):20565-79.


 8.

Effect of Aspergillus awamori-Fermented Burdock Root on Mouse Diabetes Induced by

Alloxan—Prevention of Cell Apoptosis. Kazunori Takemoto, Wakana Doi, Ayumi Zukeran, Junji Inoue, Kohji Ishihara, Noriyoshi Masuoka. Food and Nutrition Sciences, Vol.5 No.16(2014), Article ID:49228,7 pages


 9.

Engineering of pseudoislets: effect on insulin secretion activity by cell number, cell population, and microchannel networks. Kojima N, Takeuchi S, Sakai Y. Transplant Proc. Vol.46(4), p1161-65, May 2014.


10.

Evaluation of 7-O-galloyl-d-sedoheptulose, isolated from Corni Fructus, in the adipose tissue of type 2 diabetic db/db mice. Park CH., Tanaka T., Yokozawa T. Fitoterapia, Vol.89, p131-142, Sep 2013.


11.

Periaortic adipose tissue-specific activation of the renin-angiotensin system contributes to atherosclerosis development in uninephrectomized apoE-/- mice. Kawahito H., Yamada H., Irie D., Kato T., Akakabe Y., Kishida S., Takata H., Wakana N., Ogata T., Ikeda K., Ueyama T., Matoba S., Mori Y., Matsubara H. American Journal of Physiology – Heart and Circulatory Physiology, Vol.305, p667-675, Sep 2013.


12.

Effect of vitamin E on alloxan-induced mouse diabetes. Kamimura W., Doi W., Takemoto K., Ishihara K., Wang D-H., Sugiyama H., Oda S., Masuoka N. Clinical Biochemistry, Vol.46(9), p795-798, Jun 2013.


13.

Evaluation of 7-O-galloyl-d-sedoheptulose, isolated from Corni Fructus, in the adipose tissue of type 2 diabetic db/db mice. C.H.Park, T.Tanaka, T.Yokozawa. Fitoterapia,  Vol.89, p131-42, Sep 2013.


14.

Therapeutic approach for type 1 diabetes mellitus using the novel immunomodulator FTY720 (fingolimod) in combination with once-daily injection of insulin glargine in non-obese diabetic mice. T.Tsuji, M.Inoue, Y.Yoshida, T.Fujita, Y.Kaino, T.Kohno. Journal of Diabetes Investigation, Vol.3(2), p132-137, Apr 2012.


15.

Effect of vitamin E on alloxan-induced mouse diabetes. Kamimura W, Doi W, Takemoto K, Ishihara K, Wang D-H, Sugiyama H, Oda S, Masuoka N. Clinical Biochemistry, Mar 2013.


16.

Intramedullary Cavity as an Implant Site for Bioartificial Pancreas: An In Vivo Study on Diabetic Canine. Y, Kai-Chiang., W, Chang-Chin., S, Shoichiro., K, Tzong-Fu., L, Sheng-Chuan., L, Feng-Huei. Transplantation, Vol. 90(6), p604-611, Sep 2010.


17.

The in vivo performance of bioartificial pancreas in bone marrow cavity: A case report of a spontaneous diabetic feline. K, C, Yang., C, C, Wu., S, C, Lin., S, Sumi., F, H, Lin. Biochemical and Biophysical Research Communications, Vol.393(3), p362-364, Mar 2010.


18.

In vitro reprogramming of adult hepatocytes into insulin-producing cells without viral vectors . H, Motoyama., S, Ogawa., A, Kubo., S, Miwa., J, Nakayama., Y, Tagawa., S, Miyagawa. Biochemical and Biophysical Research Communications, Vol.385(1),  p123-128, Jul 2009.


19.

Efficient differentiation of insulin-producing cells from skin-derived stem cells. Guo,W.,Miao,C.,Liu,S.,Qiu,Z.,Li,J., and Duan, E. Cell Proliferation, Vol.42(1), p49-62, 2009.


20.

Enrichment of Putative Pancreatic Progenitor Cells From Mice by Sorting for Prominin1(CD133)and PDGFRb. Yuichi Hori,Miki Fukomoto,Yoshikazu Kuroda. Stem Cells;0:2008-0192v1,2008


21.

Possibility of insulin-producing cells derived from mouse embryonic stem cells for diabetes treatment. T, Ibii., H, Shimada., S, Miura., E, Fukuma., H, Sato., H, Iwata. Journal of Bioscience and Bioengineering,Vol.103(2), p140-146, Feb 2007.


22.

The dual function of hepatic SOCS3 in insulin resistance in vivo. Torisu, T., Sato, N., Yoshiga, D., Kobayashi, T., Yoshioka, T., Mori, H., Iida, M. and Yoshimura, A. Genes to Cells, 12, p143-154, 2007.


23.

Prolonged remission of diabetes by regeneration of bold italic beta cells in diabetic mice treated with recombinant adenoviral vector expressing glucagon-like peptide-1. Liu, M.J., Shin, S., Li, N., Shigehara, T., Lee, Y.S., Yoon, J.W., and Jun H.S. Molecular Therapy 15: p86-93, 2007.


24.

Possibility of insulin-producing cells derived from mouse embryonic stem cells for diabetes treatment. Ibii, T., Shimada, H, Miura, S., Fukuma, E.,Sato, H.,and Iwata,H. J Bioscience Bioengineering 103: p140-146, 2007.


25.

A human b-cell line for transplantation therapy to control type 1 diabetes. Narushima, M., Kobayashi, N., Okitsu, T., Tanaka, Y., Li, S.A., Chen, Y., Miki, A., Tanaka, K., Nakaji, S., Takei, K., Gutierrez, A.S., Rivas-Carrillo, J.D., Navarro-Alvarez, N., Jun, H.S., Westerman, K.A., Noguchi, H., Lakey, J.R.T.,, Leboulch, P., Tanaka, N., and Yoon, J.W. Nature Biotechnology, Vol. 23(10), p1274-1282, 2005.


产品编号 产品名称 产品规格 产品等级
635-07239 (AKRCP-031)LBIS® Mouse C-peptide ELISA kit (U-type)
LBIS®小鼠 C-肽 ELISA试剂盒(U型) 
96 tests

LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型) LBIS® Insulin-Rat (H type)

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Insulin-Rat (H type)LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Rat (H type)

LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型)

  胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

  A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含Zn离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。

  肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

  胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点

 

● 有色缓冲液(蓝色)、容易确认分装后的孔

● 短时间测定(总的反应时间:3小时)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 操作简便,不需要特别的预处理

 

 

◆构成

 

组成

状态

容量

(A)   抗体固相化 96 孔板

洗净后使用

96   wells(8×12)/1 块

(B)   胰岛素标准溶液(大鼠)(200 ng/mL

稀释后使用

300 μL/1 瓶

(C)   缓冲液(蓝色)

即用

60 mL/1 瓶

(D)  生物素结合抗胰岛素抗体

稀释后使用

200 μL/1 瓶

(E)   过氧化物・抗生物素蛋白结合物

稀释后使用

200 μL/1 瓶

(F)   显色液(TMB)

即用

12 mL/1 瓶

(H)  反应终止液(1M   H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

◆样品信息

大鼠的血清•血浆•培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液



◆测量范围

0.5~100 ng/mL(标准曲线范围)

◆Validation data

精度测试(检测内变动系数)

 

样品

A

B

C

1

2.73

12.9

86.7

2

2.78

12.6

86.2

3

2.78

12.8

85.6

4

2.78

12.6

85.2

5

2.73

12.6

85.9

mean

2.76

12.7

85.9

SD

0.025

0.147

0.575

CV(%)

0.9

1.2

0.7

单位:ng/mL

 

再现性测试(检测内变动系数)

 

测量日/样品

D

E

F

第0天

3.34

25.5

70.3

第1天

3.28

25.7

70.3

第2天

3.15

25.2

71.6

mean

3.26

25.5

70.7

SD

0.097

0.280

0.765

CV(%)

3.0

1.1

1.1

单位:ng/mL n=2

 

添加回收测试

 

样品G

添加量

实测值

回收量

回收率(%)

0.00

31.3

20.0

51.2

19.9

99.5

40.0

73.1

41.8

105

60.0

94.3

63.0

105

单位:ng/mL n=2


样品H

添加量

实测值

回收量

回收率(%)

0.00

1.36

1.21

2.58

1.22

101

2.46

3.75

2.39

97.2

3.46

4.64

3.28

94.8

单位:ng/mL n=2

 

稀释直线性测试

 

用稀释缓冲液分3次连续稀释2个血清样品的测量结果,直线回归方程的R2在0.9966~0.9995之间。

相关资料


LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Rat (H type) LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Rat (H type) LBIS® 大鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Rat (H type)
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献


1.

Duodenal-jejunal bypass improves diabetes and liver steatosis via enhanced glucagon-like peptide-1 elicited by bile acids. Kashihara H, Shimada M, Kurita N, Sato H, Yoshikawa K, Higashijima J, Chikakiyo M, Nishi M, Takasu C. J Gastroenterol Hepatol. Vol.30(2), p308-15, Feb 2015.


2.

Improving Effects of Narazuke Lees on Fatty Liver of Rats Induced by High-Fat and High-Cholesterol Diets. Nakasa T, Yamagami S, Tanaka T, Tanaka H, Hariu H, Okinaka O. Food Science and Technology Research, Vol.20 (2014), No. 4, p849-857.


3.

Duodenal-jejunal bypass improves diabetes and liver steatosis via enhanced glucagon-like peptide-1 elicited by bile acids. Kashihara H, Shimada M, Kurita N, Sato H, Yoshikawa K, Higashijima J, Chikakiyo M, Nishi M, Takasu C. J Gastroenterol Hepatol. Aug 2014.


4.

Effect of diets with different fat contents on the development of diabetes in female Zucker diabetic fatty rat with leptin mutation. Kohlerova, Renata; Sznapkova, Martina; Slavkovsky, Rastislav; Jiroutova, Alena. Acta Veterinaria Brno, Vol.82(3), p289-296, 2013.


5.

Regulation of oxidative stress and inflammation by hepatic adiponectin receptor 2 in an animal model of nonalcoholic steatohepatitis. Matsunami,T.,Sato,Y.,Ariga,S.,Sato,T.,Kashimura,H.,Hasegawa,Y.,Yukawa, M. Int J Clin Exp Pathol. Vol.3(5), p472-481, 2010.


产品编号 产品名称 产品规格 产品等级
637-10629 (AKRIN-010H)LBIS® Rat Insulin ELISA Kit(H-type)
LBIS® 大鼠胰岛素 ELISA试剂盒(H型) 
96 tests

LBIS® 大鼠胰岛素 ELISA 试剂盒(T 型) LBIS® Insulin-Rat-T

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Insulin-Rat-TLBIS® 大鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Rat-T

LBIS® 大鼠胰岛素 ELISA 试剂盒(T 型)

  胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

  A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含 Zn 离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。

肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点

● 短时间测定(总的反应时间:3小时)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 操作简便,不需要特别的预处理

● 有效期限为12个月

◆构成

组成

状态

容量

(A) 抗体固相化 96 孔板

洗净后使用

96   wells(8×12)/1 块

(B) 胰岛素标准溶液(大鼠)(200 ng/mL)

稀释后使用

25 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 生物素结合抗胰岛素抗体

稀释后使用

10 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

20 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

 

◆样品信息

大鼠的血清•血浆•培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液

◆测量范围

0.156~10 ng/mL(标准曲线范围)

◆Validation data

精度测试(检测内变动系数)

 

样品

A

B

C

D

1

0.589

1.211

2.600

4.991

2

0.568

1.228

2.600

4.971

3

0.568

1.228

2.532

5.036

4

0.557

1.211

2.538

5.026

5

0.557

1.253

2.582

4.925

6

0.578

1.220

2.563

4.880

7

0.578

1.228

2.618

5.031

8

0.536

1.228

2.618

4.885

mean

0.566

1.226

2.581

4.968

SD

0.0165

0.0131

0.0340

0.0645

CV(%)

2.92

1.07

1.32

1.30

单位:ng/mL

 

 

再现性测试(检测内变动系数)

 

测量日/样品

E

F

G

第0天

6.74

3.31

1.16

第1天

6.69

3.25

1.22

第2天

6.23

3.21

1.21

mean

6.55

3.25

1.20

SD

0.2792

0.0479

0.0325

CV(%)

4.3

1.5

2.7

单位:ng/mL n=5

 

 

添加回收测试

 

样品H

添加量

理论值

实测值

回收率(%)

0

0.996

0.500

1.496

1.484

99.2

1.000

1.996

2.048

103

2.000

2.996

2.779

92.7

单位:ng/mL

 

样品I

添加量

理论值

实测值

回收率(%)

0

1.086

0.500

1.586

1.562

98.5

1.000

2.086

2.061

98.8

2.000

3.086

2.753

89.2

单位:ng/mL

 

样品J

添加量

理论值

实测值

回收率(%)

0

1.160

0.500

1.660

1.637

98.6

1.000

2.160

2.054

95.1

2.000

3.166

2.963

93.6

单位:ng/mL

 

 

稀释直线性测试

 

用稀释缓冲液分4次连续稀释2个血清样品的测量结果,直线回归方程的R2在0.9983~0.9992之间。

相关资料


LBIS® 大鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Rat-T LBIS® 大鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Rat-T LBIS® 大鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Rat-T
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

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Effects of electrical microstimulation of peripheral sympathetic nervous fascicle on glucose uptake in rats. Sato D, Shinzawa G, Kusunoki M, Matsui T, Sasaki H, Feng Z, Nishina A, Nakamura T. Journal of Artificial Organs, Mar 2013.


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Quercetin intake during lactation modulates the AMP-activated protein kinase pathway in the livers of adult male rat offspring programmed by maternal protein restriction. Sato S., Mukai Y., Saito T. The Journal of Nutritional Biochemistry, Vol.24(1), p118-123, Jan 2013.


75.

Reduction of reactive oxygen species ameliorates metabolism-secretion coupling in islets of diabetic GK rats by suppressing lactate overproduction. Sasaki M, Fujimoto S, Sato Y, Nishi Y, Mukai E, Yamano G, Sato H, Tahara Y, Ogura K, Nagashima K and Inagaki N. Diabetes, January 24, 2013 , In press.


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Derangement of ghrelin secretion after long-term high-fat diet feeding in rats. Sugiishi A, Kimura M, Kamiya R, Ueki S, Yoneya M, Saito Y, Saito H. Hepatology Research, 2013, In press.

 

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Proteomic and bioinformatic analysis of membrane proteome in type 2 diabetic mouse liver. Kim G-H, Park E C, Yun S-H, Hong Y, Lee D-G, Shin E-Y, Jung J, Kim Y H, Lee K-B, Jang I-S, Lee Z-W, Chung Y-H, Choi J-S, Cheong C, Kim S, Kim S II. PROTEOMICS, 2013, In press.


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A Novel Rat Model of Type 2 Diabetes: The Zucker Fatty Diabetes Mellitus ZFDM Rat. Yokoi N, Hoshino M, Hidaka S, Yoshida E, Beppu M, Hoshikawa R, Sudo K, Kawada A, Takagi S and Seino S. Journal of Diabetes Research, Vol.2013 (2013)


79.

Urinary cystatin C as a biomarker for diabetic nephropathy and its immunohistochemical localization in kidney in Zucker diabetic fatty (ZDF) rats. Togashi Y, Miyamoto Y. Experimental and Toxicologic Pathology,Available online 12 Jul 2012.


80.

Artemisia campestris leaf extract alleviates early diabetic nephropathy in rats by inhibiting protein oxidation and nitric oxide end products. Mediha S, Hamadi F, Nejla S, Yassine C, Mohamed M, Najiba Z. Pathology – Research and Practice, Vol.208(3), p157-162, Mar 2012.


81.

Fenugreek with reduced bitterness prevents diet-induced metabolic disorders in rats. Muraki E, Chiba H, Taketani K, Hoshino S, Tsuge N, Tsunoda N and Kasono K. Lipids in Health and Disease, Vol.11(58), 2012.


82.

Oral Ingestion of Aloe vera Phytosterols Alters Hepatic Gene Expression Profiles and Ameliorates Obesity-Associated Metabolic Disorders in Zucker Diabetic Fatty Rats. E. Misawa., M. Tanaka., K. Nomaguchi., K. Nabeshima., M. Yamada., T. Toida., and K. Iwatsuki. J. Agric. Food Chem., 2012, 60 (11), pp 2799-2806


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 Myocardial Infarction-Prone Watanabe Heritable Hyperlipidemic Rabbits with Mesenteric Fat Accumulation Are a Novel Animal Model for Metabolic Syndrome. M. Shiomi., T. Kobayashi., N. Kuniyoshi., S. Yamada., T. Ito. Pathobiology 2012;Vol. 79 No. 6 P329-338


84.

High-fat diet-induced reduction of peroxisome proliferator-activated receptor-γ coactivator-1α messenger RNA levels and oxidative capacity in the soleus muscle of rats with metabolic syndrome. F. Nagatomo., H. Fujino., H. Kondo., I. Takeda., K. Tsuda., A. Ishihara. Nutrition Research, Vol. 32, Issue 2, February 2012, Pages 144-151


85.

The effects of running exercise on oxidative capacity and PGC-1α mRNA levels in the soleus muscle of rats with metabolic syndrome. F. Nagatomo., H. Fujino., H. Kondo., M. Kouzaki., N. Gu., I. Takeda., K. Tsuda., and A. Ishihara. The Journal of Physiological Sciences, Vol. 62, Number 2 (2012), 105-114


86.

A Comparative Study of Gastric Banding and Sleeve Gastrectomy in an Obese Diabetic Rat Model. T. Masuda., M. Ohta., T. Hirashita., Y. Kawano., H. Egucji., K. Yada., Y. Iwashita., S. Kitano. Obesity Surgery, Published online:27 August 2011


87.

Site dependency of fatty acid composition in adipose triacylglycerol in rats and its absence as a result of high-fat feeding. D. Sato., T. Nakamura., K. Tsutsumi., G. Shinzawa., T. Karimata., T. Okawa., Z. Fengc., and M. Kusunoki. Metabolism.Article in Press


88.

Dietary fructo-oligosaccharides improve insulin sensitivity along with the suppression of adipocytokine secretion from mesenteric fat cells in rats. A. Shinoki., and H. Hara. British Journal of Nutrition.Published online :02 June 2011.


89.

Food restriction improves glucose and lipid metabolism through Sirt1 expression: A study using a new rat model with obesity and severe hypertension. K. Takemori.,T. Kimura.,N. Shirasaka.,T. Inoue.,K. Masuno., and H. Ito. Life Sciences.Vol.88, Issues 25-26, 1088-1094. 2011


90.

Enhanced Urinary Bladder, Liver and Colon Carcinogenesis in Zucker Diabetic Fatty Rats in a Multiorgan Carcinogenesis Bioassay: Evidence for Mechanisms Involving Activation of PI3K Signaling and Impairment of P53 on Urinary Bladder Carcinogenesis. N. Ishii., M. Wei., A. Kakehashi., K. Doi., S. Yamano., M. Inaba., and H.Wanibuchi. Journal of Toxicologic Pathology .Vol. 24 (2011) , No. 1 pp.25


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Maternal low-protein diet suppresses vascular and renal endothelial nitric oxide synthase phosphorylation in rat offspring independent of a postnatal fructose diet. S. Sato.,Y. Mukai., and T. Norikura. Journal of Developmental Origins of Health and Disease (2011), 2: 168-175


92.

Combined Effects of Short-term Calorie Restriction and Exercise on Insulin Action in Normal Rats. H,Y,Jiang.,T,Koike.,P,Li.,Z,H,Wang.,Y,Kawata.,Y,Oshida. Horm Metab Res 2010; 42(13): 950-954


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Dietary Hesperidin Exerts Hypoglycemic and Hypolipidemic Effects in Streptozocin-Induce Marginal Type 1 Diabetic Rats. Akiyama,S., Katsumata,S., Suzuki,K., Ishimi,Y.,Wu,J., and Uehara,M.. J Clin Biochem Nutr.January;46(1):87-92.2010


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Hypoglycemic and Hypolipidemic Effects of Hesperidin and Cyclodextrin-Clathrated Hesperetin in Goto-Kakizaki Rats with Type 2 Diabetes. Akiyama,S., Katsumata,S., Suzuki,K., Nakayama,Y., Ishimi,Y. and Uehara,M. Bioscience,Biotechnology,and Biochemistry.Vol.73,No.12 pp.2779-2782(2009)

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Anti-Diabetic Effects of Pumpkin and Its Components,Trigonelline and Nicotinic Acid,on Goto-Kakizaki Rats. Yoshinari,O.,Sato,H.and Igarashi,K. Bioscience,Biotechnology,and Biochemistry.Vol.73,No5pp.1033-1041,2009


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Dietary Phosphatidylinositol Prevents the Development of Nonalcoholic Fatty Liver Disease in Zucker(fa/fa)Rats Shirouchi,B.,Nagao,K.,Inoue,N.,Furuya,K.,Koga,S.,Matsumoto,H. and Yanagita,T. J.Agric.Food Chem.56,2375-2379,2008


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Investigation of the anti-obesity action of licorice flavonoid oil in diet-induced obese rats. Kamisoyama,H.,Honda,K.,Tominaga,Y.,Yokota,S.,Hasegawa,S. Bioscience.Biotechnology and Biochemistry 72.(12)3225-3231,2008


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Erythrophagocytosis by Liver Macrophages(Kupffer Cells)Promotes Oxidative Stress, Inflammation,and Fibrosis in a Rabbit Model of Steatohepatitis. Otogawa,K.,Kinoshita,K.,Fujii,H.,Sakabe,M.,Shiga,R.,Nakatani,K.,Ikeda,K.,Nakajima,Y.,Ikura,Y.,Ueda,M., Arakawa,T.,Hato,F., and Kawada,N. American Journal of Pathology. 170:967-980, 2007


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Effect of 5-Campestenone (24-methylcholest-5-en-3-one) on Zucker Diabetic Fatty Rats as a Type 2 Diabetes Mellitus Model. R.Konno, Y.,Kaneko, K.,Suzuki, Y.,Matsui. Horm Metab Res ; 37(3): 79-83,2005

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产品编号 产品名称 产品规格 产品等级
631-01479 (AKRIN-010T) LBIS® Rat Insulin ELISA Kit(T-type)
LBIS® 大鼠胰岛素 ELISA试剂盒(T型) 
96 tests

LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型) LBIS® Insulin-Mouse-T

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Insulin-Mouse-TLBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Mouse-T

LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)

LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Mouse-T

  

胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

  A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含 Zn 离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。

肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点

● 短时间测定(总的反应时间:3小时)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 操作简便,不需要特别的预处理

● 有效期限为 12 个月

◆构成

组成部分

状态

容量

(A) 抗体固相化 96孔板

洗净后使用

96 wells(8×12)/1 块

(B) 胰岛素标准溶液(小鼠)(200 ng/mL)

稀释后使用

25 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 生物素结合抗胰岛素抗体

稀释后使用

10 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

20 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应终止液(1M   H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

◆样品信息

小鼠的血清、血浆、培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液

 

◆测量范围

0.156~10 ng/mL(标准曲线范围)

◆Validation data

精度测试(检测内变动系数)

样品

A

B

C

D

mean

0.882

1.15

3.67

5.25

SD

0.0245

0.0213

0.0649

0.0792

CV(%)

2.78

1.87

1.77

1.51

单位:ng/mL n=10

 

再现性测试(检测内变动系数)

测量日/样品

E

F

G

第0天

5.253

1.224

0.513

第1天

5.322

1.312

0.523

第2天

5.365

1.269

0.512

第3天

5.362

1.281

0.535

mean

5.326

1.272

0.521

SD

0.0520

0.0366

0.0109

CV(%)

3.31

3.76

4.65

单位:ng/mL n=3

 

加标回收测试

 

样品H

添加量

实测值

回收量

回收率(%)

0

1.350

0.25

1.593

0.243

97.2

0.50

1.841

0.491

98.2

0.75

2.065

0.715

95.3

1.00

2.299

0.949

94.9

单位:ng/mL n=3

 

样品I

添加量

实测值

回收量

回收率(%)

0

1.941

0.50

2.496

0.505

101

0.75

2.728

0.737

98.3

1.00

2.955

0.964

96.4

1.50

3.431

1.440

96.0

单位:ng/mL n=3

 

稀释直线性测试

 

用稀释缓冲液分3次连续稀释3个血清样品的测量结果,直线回归方程的 R2在 0.993~0.999 之间。

相关资料


LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Mouse-T LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Mouse-T LBIS® 小鼠胰岛素 ELISA 试剂盒(T 型)                              LBIS® Insulin-Mouse-T
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献



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Oxytocin Protects against Stress-Induced Cell Death in Murine Pancreatic β-Cells. Watanabe S, Wei FY, Matsunaga T, Matsunaga N, Kaitsuka T, Tomizawa K. Sci Rep. 2016 May 4;6:25185.


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Loss of circadian rhythm of circulating insulin concentration induced by high-fat diet intake is associated with disrupted rhythmic expression of circadian clock genes in the liver. Honma K, Hikosaka M, Mochizuki K, Goda T. Metabolism. 2016 Apr;65(4):482-91


35.

Sodium alginate prevents progression of non-alcoholic steatohepatitis and liver carcinogenesis in obese and diabetic mice. Miyazaki T, Shirakami Y, Kubota M, Ideta T, Kochi T, Sakai H, Tanaka T, Moriwaki H, Shimizu M. Oncotarget. 2016 Mar 1;7(9):10448-58.


36.

Obesity-induced DNA released from adipocytes stimulates chronic adipose tissue inflammation and insulin resistance. Nishimoto S, Fukuda D, Higashikuni Y, Tanaka K, Hirata Y, Murata C, Kim-Kaneyama JR, Sato F, Bando M, Yagi S, Soeki T, Hayashi T, Imoto I, Sakaue H, Shimabukuro M, Sata M. Sci Adv. 2016 Mar 25;2(3):e1501332


37.

Fatty Liver and Insulin Resistance in the Liver-Specific Knockout Mice of Mitogen Inducible Gene-6. Park BK, Lee EA, Kim HY, Lee JC, Kim KS, Jeong WH, Kim KY, Ku BJ, Rhee SD. J Diabetes Res. 2016;2016:1632061


38.

Reactive sulfur species regulate tRNA methylthiolation and contribute to insulin secretion. Takahashi N, Wei FY, Watanabe S, Hirayama M, Ohuchi Y, Fujimura A, Kaitsuka T, Ishii I, Sawa T, Nakayama H, Akaike T, Tomizawa K.


39.

Effects of caloric restriction on O-GlcNAcylation, Ca(2+) signaling, and learning impairment in the hippocampus of ob/ob mice. Jeon BT, Heo RW, Jeong EA, Yi CO, Lee JY, Kim KE, Kim H, Roh GS. Neurobiol Aging. 2016 Aug;44:127-37.


40.

Chronic Repression of mTOR Complex 2 Induces Changes in the Gut Microbiota of Diet-induced Obese Mice. Jung MJ, Lee J, Shin NR, Kim MS, Hyun DW, Yun JH, Kim PS, Whon TW, Bae JW. Sci Rep. 2016 Jul 29;6:30887.


41.

Single ingestion of soy β-conglycinin induces increased postprandial circulating FGF21 levels exerting beneficial health effects. Hashidume T, Kato A, Tanaka T, Miyoshi S, Itoh N, Nakata R, Inoue H, Oikawa A, Nakai Y, Shimizu M, Inoue J, Sato R. Sci Rep. 2016 Jun 17;6:28183.


42.

Paraventricular NUCB2/Nesfatin-1 Supports Oxytocin and Vasopressin Neurons to Control Feeding Behavior and Fluid Balance in Male Mice. Nakata M, Gantulga D, Santoso P, Zhang B, Masuda C, Mori M, Okada T, Yada T. Endocrinology. 2016 Jun;157(6):2322-32.


43.

Oxytocin Protects against Stress-Induced Cell Death in Murine Pancreatic β-Cells. Watanabe S, Wei FY, Matsunaga T, Matsunaga N, Kaitsuka T, Tomizawa K. Sci Rep. 2016 May 4;6:25185.


44.

Loss of circadian rhythm of circulating insulin concentration induced by high-fat diet intake is associated with disrupted rhythmic expression of circadian clock genes in the liver. Honma K, Hikosaka M, Mochizuki K, Goda T. Metabolism. 2016 Apr;65(4):482-91.


45.

Protective effect of vitamin E against alloxan-induced mouse hyperglycemia. Takemoto K, Doi W, Masuoka N. Biochim Biophys Acta. 2016 Apr;1862(4):647-50.


46.

Castration influences intestinal microflora and induces abdominal obesity in high-fat diet-fed mice. Harada N, Hanaoka R, Horiuchi H, Kitakaze T, Mitani T, Inui H, Yamaji R. Sci Rep. 2016 Mar 10;6:23001.


47.

Pharmacological Inhibition of Monoacylglycerol O-Acyltransferase 2 Improves Hyperlipidemia, Obesity, and Diabetes by Change in Intestinal Fat Utilization. Take K, Mochida T, Maki T, Satomi Y, Hirayama M, Nakakariya M, Amano N, Adachi R, Sato K, Kitazaki T, Takekawa S. PLoS One. 2016 Mar 3;11(3):e0150976.


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GADD34-deficient mice develop obesity, nonalcoholic fatty liver disease, hepatic carcinoma and insulin resistance Naomi Nishio and Ken-ichi Isobe Sci Rep. 2015; 5: 13519.


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Patterns of Brain Activation and Meal Reduction Induced by Abdominal Surgery in Mice and Modulation by Rikkunshito Lixin Wang, Sachiko Mogami, Seiichi Yakabi, Hiroshi Karasawa, Chihiro Yamada, Koji Yakabi, Tomohisa Hattori, and Yvette Taché PLoS One. 2015; 10(9): e0139325.


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Hot water extracts of edible Chrysanthemum morifolium Ramat. exert antidiabetic effects in obese diabetic KK-Ay mice Yamamoto J, Tadaishi M, Yamane T, Oishi Y, Shimizu M, Kobayashi-Hattoria K. Bioscience, Biotechnology, and Biochemistry, Vol.79(7), 2015.


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Dietary obacunone supplementation stimulates muscle hypertrophy, and suppresses hyperglycemia and obesity through the TGR5 and PPARγ pathway. Horiba T, Katsukawa M, Mita M, Sato R. Biochem Biophys Res Commun. Vol.463(4), p846-52, Aug. 2015.


52.

Hepatic STAMP2 alleviates high fat diet-induced hepatic steatosis and insulin resistance. Kim HY, Park SY, Lee MH, Rho JH, Oh YJ, Jung HU, Yoo SH, Jeong NY, Lee HJ, Suh S, Seo SY, Cheong J, Jeong JS, Yoo YH. J Hepatol. Vol.63(2), p477-85, Aug 2015.


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Optogenetic control of insulin secretion by pancreatic β-cells in vitro and in vivo. Kushibiki T, Okawa S, Hirasawa T, Ishihara M. Gene Ther. Vol.22(7), p553-9, Jul 2015.


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Preventive effects of astaxanthin on diethylnitrosamine-induced liver tumorigenesis in C57/BL/KsJ-db/db obese mice. Ohno T, Shimizu M, Shirakami Y, Miyazaki T, Ideta T, Kochi T, Kubota M, Sakai H, Tanaka T, Moriwaki H. Hepatol Res. Jul 2015


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Effects of liquid konjac on parameters related to obesity in diet-induced obese mice. Aoe S, Kudo H, Sakurai S. Biosci Biotechnol Biochem. Vol.79(7), p1141-6, Jul 2015.


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Alteration of gut microbiota by vancomycin and bacitracin improves insulin resistance via glucagon-like peptide 1 in diet-induced obesity. Hwang I, Park YJ, Kim YR, Kim YN, Ka S, Lee HY, Seong JK, Seok YJ, Kim JB. FASEB J. Vol.29(6), p2397-411, Jun 2015.


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PRMT4 is involved in insulin secretion via the methylation of histone H3 in pancreatic β cells. Kim JK, Lim Y, Lee JO, Lee YS, Won NH, Kim H, Kim HS. J Mol Endocrinol.Vol.54(3), p315-24, Jun 2015.


58.

Hepatic NPC1L1 overexpression ameliorates glucose metabolism in diabetic mice via suppression of gluconeogenesis. Kurano M, Hara M, Satoh H, Tsukamoto K. Metabolism. Vol.64(5), p588-96, May 2015.


59.

Chronic high intake of quercetin reduces oxidative stress and induces expression of the antioxidant enzymes in the liver and visceral adipose tissues in mice. Kobori M, Takahashi Y, Akimoto Y, Sakurai M, Matsunaga I, Nishimuro H, Ippoushi K, Oike H, Ohnishi-Kameyama M. Journal of Functional Foods, Vol.15, p551–560, May 2015.


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Effects of quercetin derivatives from mulberry leaves: Improved gene expression related hepatic lipid and glucose metabolism in short-term high-fat fed mice. Sun X, Yamasaki M, Katsube T, Shiwaku K. Nutr Res Pract. Vol.9(2), p137-43, Apr 2015.


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Insulin Release from the Beta Cells in Acatalasemic Mice Is Highly Susceptible to Alloxan-Induced Oxidative Stress. Kazunori Takemoto, Wakana Doi, Ken Kataoka, Kohji Ishihara, Da-Hong Wang., Hitoshi Sugiyama, Noriyoshi Masuoka. JDM, Vol.5 No.2, May 2015


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Titanium dioxide nanoparticles increase plasma glucose via reactive oxygen species-induced insulin resistance in mice. Hu H, Guo Q, Wang C, Ma X, He H, Oh Y, Feng Y, Wu Q, Gu N. J Appl Toxicol. Mar 2015 .


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Compensatory hyperinsulinemia in high-fat diet-induced obese mice is associated with enhanced insulin translation in islets. Kanno A, Asahara S, Masuda K, Matsuda T, Kimura-Koyanagi M, Seino S, Ogawa W, Kido Y.  Biochem Biophys Res Commun. Vol.13;458(3), p681-6. Mar 2015.


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Optogenetic control of insulin secretion by pancreatic β-cells in vitro and in vivo. Kushibiki T, Okawa S, Hirasawa T, Ishihara M. Gene Ther. Mar 2015.


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Compensatory hyperinsulinemia in high-fat diet-induced obese mice is associated with enhanced insulin translation in islets. Kanno A, Asahara S, Masuda K, Matsuda T, Kimura-Koyanagi M, Seino S, Ogawa W, Kido Y. Biochem Biophys Res Commun. Vol.458(3), p681-6, Mar 2015.


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Essential role of mitochondrial Ca2+ uniporter in the generation of mitochondrial pH gradient and metabolism-secretion coupling in insulin-releasing cells. Quan X, Nguyen TT, Choi SK, Xu S, Das R, Cha SK, Kim N, Han J, Wiederkehr A, Wollheim CB, Park KS. J Biol Chem. Vol.290(7), p4086-96, Feb 2015.


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Endogenous Interleukin 18 Suppresses Hyperglycemia and Hyperinsulinemia during the Acute Phase of Endotoxemia in Mice. Yamashita H, Aoyama-Ishikawa M, Takahara M, Yamauchi C, Inoue T, Miyoshi M, Maeshige N, Usami M, Nakao A, Kotani J. Surg Infect (Larchmt). 2015 Feb;16(1):90-6.


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 Hot water extracts of edible Chrysanthemum morifolium Ramat. exert antidiabetic effects in obese diabetic KK-Ay mice. Junpei Yamamoto, Miki Tadaishi, Takumi Yamane, Yuichi Oishi, Makoto Shimizu & Kazuo Kobayashi-Hattoria. Bioscience, Biotechnology, and Biochemistry, Published online: 10 Feb 2015


69.

Alteration of gut microbiota by vancomycin and bacitracin improves insulin resistance via glucagon-like peptide 1 in diet-induced obesity. Hwang I, Park YJ, Kim YR1, Kim YN, Ka S, Lee HY, Seong JK, Seok YJ, Kim JB. FASEB J. Feb 2015.


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Titanium dioxide nanoparticles increase plasma glucose via reactive oxygen species-induced insulin resistance in mice. Hu H, Guo Q, Wang C, Ma X, He H, Oh Y, Feng Y, Wu Q, Gu N. J Appl Toxicol. Mar 2015.


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Ashitaba (Angelica keiskei) extract prevents adiposity in high-fat diet-fed C57BL/6 mice. Zhang T, Yamashita Y, Yasuda M, Yamamoto N, Ashida H. Food Funct. Vol.6(1), p134-144, Jan 2015.


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Dietary nitrite supplementation improves insulin resistance in type 2 diabetic KKAy mice Ohtake K, Nakano G, Ehara N, Sonoda K, Ito J, Uchida H, Kobayashi J. Nitric Oxide, Vol.44, p31–38, Jan 2015.


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Salicornia herbacea prevents weight gain and hepatic lipid accumulation in obese ICR mice fed a high-fat diet. Pichiah PT, Cha YS. J Sci Food Agric. Dec 2014.


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Salacia reticulata has therapeutic effects on obesity. Shimada T, Nakayama Y, Harasawa Y, Matsui H, Kobayashi H, Sai Y, Miyamoto K, Tomatsu S, Aburada M. J Nat Med. Vol.68(4), p668-676, Oct 2014.Salicornia herbacea prevents weight gain and hepatic lipid accumulation in obese ICR mice fed a high-fat diet. Pichiah PT1, Cha YS. J Sci Food Agric. Dec 2014.


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Ghrelin administered spinally increases the blood glucose level in mice. Sim Y-B., Park S-H., Kim S-S., Kim C-H., Kim S-J., Lim S-M., Jung J-S., Suh H-W. Peptides, Vol.54, p162-165, Apr 2014.

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Chronic exposure to valproic acid promotes insulin release, reduces KATP channel current and does not affect Ca2+ signaling in mouse islets. Manaka K., Nakata M., Shimomura K., Rita RS., Maejima Y., Yoshida M., Dezaki K., Kakei M., Yada T. The Journal of Physiological Sciences, Vol.64(1), p77-83, Jan 2014.


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Impaired Lipid and Glucose Homeostasis in Hexabromocyclododecane-Exposed Mice Fed a High-Fat Diet. Yanagisawa R., Koike E., Win-Shwe TT., Yamamoto M. and Takano H. ENVIRONMENTAL HEALTH PERSPECTIVES, Jan 2014.


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Lipid-Lowering Effects of Pediococcus acidilactici M76 Isolated from Korean Traditional Makgeolli in High Fat Diet-Induced Obese Mice. Moon Y-J., Baik S-H. and Cha Y-S. Nutrients, Vol.6(3), p1016-1028, 2014.


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Azilsartan, an angiotensin II type 1 receptor blocker, restores endothelial function by reducing vascular inflammation and by increasing the phosphorylation ratio Ser1177/Thr497 of endothelial nitric oxide synthase in diabetic mice. Matsumoto S., Shimabukuro M., Fukuda D., Soeki T., Yamakawa K., Masuzaki H. and Sata M. Cardiovascular Diabetology, 13:30, 2014.


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Intake of mulberry 1-deoxynojirimycin prevents diet-induced obesity through increases in adiponectin in mice. T.Tsuduki, I.Kikuchi, T.Kimura, K.Nakagawa, T.Miyazawa. Food Chemistry, Vol.139(1-4), p16-23, Aug 2013.


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Chronic treatment with novel GPR40 agonists improve whole-body glucose metabolism based on the glucose-dependent insulin secretion. H.Tanaka, S.Yoshida, H.Oshima, H.Minoura, K.Negoro, T.Yamazaki, S.Sakuda, F.Iwasaki, T.Matsui and M. Shibasaki. JPET, Jul 2013.


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Contribution of insulin signaling to the regulation of pancreatic beta-cell mass during the catch-up growth period in a low birth weight mouse model. Y.Yoshida, M.Fuchita, M.Kimura-Koyanagi, A.Kanno, T.Matsuda, S.Asahara, N.Hashimoto, T.Isagawa, W.Ogawa, H.Aburatani, T.Noda, S.Seino, M.Kasuga, Y.Kido. Diabetology International, Jul 2013.


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Differential contribution of insulin and amino acids to the mTORC1-autophagy pathway in the liver and muscle. T.Naito, A.Kuma and N.Mizushima. The Journal of Biological Chemistry, Jun 2013.


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Apelin Inhibits Diet-Induced Obesity by Enhancing Lymphatic and Blood Vessel Integrity. M.Sawane, K.Kajiya, H.Kidoya, M.Takagi, F.Muramatsu and N.Takakura. Diabetes, Vol.62(6), p1970-1980, Jun 2013.


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Ras-related C3 botulinum toxin substrate 1 (RAC1) regulates glucose-stimulated insulin secretion via modulation of F-actin. S.Asahara, Y.Shibutani, K.Teruyama, H.Y.Inoue, Y.Kawada, H.Etoh, T.Matsuda, M.Kimura-Koyanagi, N.Hashimoto, M.Sakahara, W.Fujimoto, H.Takahashi, S.Ueda, T.Hosooka, T.Satoh, H.Inoue, M.Matsumoto, A.Aiba, M.Kasuga, Y.Kido. Diabetologia, Vol.56(5), p1088-1097, May 2013.


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Effects of hydrophilic statins on renal tubular lipid accumulation in diet-induced obese mice. K.Gotoh, T.Masaki, S.Chiba, H.Ando, K.Fujiwara, T.Shimasaki, Y.Tawara, I.Toyooka, K.Shiraishi, K.Mitsutomi, M.Anai, E.Itateyama, J.Hiraoka, K.Aoki, N.Fukunaga, T.Nawata, T.Kakuma. Obesity Research & Clinical Practice, May 2013.


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Amyloid-β Induces Hepatic Insulin Resistance In Vivo via JAK2. Y.Zhang, B.Zhou, B.Deng, F.Zhang, J.Wu, Y.Wang, Y.Le and Q.Zhai. Diabetes, Vol.62(4), p1159-1166, Apr 2013.


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Histidine augments the suppression of hepatic glucose production by central insulin action

Kimura K, Nakamura Y, Inaba Y, Matsumoto M, Kido Y, Asahara S, Matsuda T, Watanabe H, Maeda A, Inagaki F, Mukai C, Takeda K, Akira S, Ota T, Nakabayashi H, Kaneko S, Kasuga M and Inoue H.

Diabetes, Vol.62(4), p1003-1004, Apr 2013


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Improved transplantation outcome through delivery of DNA encoding secretion signal peptide-linked glucagon-like peptide-1 into mouse islets

Chae H Y, Lee M, Hwang H J, Kim H A, Kang J G, Kim C S, Lee S J, Ihm S-H.

Transplant International, Vol.26(4), p443-452, Apr 2013.


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Histidine augments the suppression of hepatic glucose production by central insulin action

K.Kimura, Y.Nakamura, Y.Inaba, M.Matsumoto, Y.Kido, S.Asahara, T.Matsuda, H.Watanabe, A.Maeda, F.Inagaki, C.Mukai, K.Takeda, S.Akira, T.Ota, H.Nakabayashi, S.Kaneko, M.Kasuga and H.Inoue. Diabetes, Mar 2013.


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Wogonin ameliorates hyperglycemia and dyslipidemia via PPARα activation in db/db mice without adverse side effects. Bak E-J, Kim J-H, Lee D-E, Choi Y-H, Kim J M, Woo G-H, Cha J-H, Yoo Y-J. Clinical Nutrition, Available online 26, Mar 2013.


92.

Extracellular Signal-Regulated Kinase in the Ventromedial Hypothalamus Mediates Leptin-Induced Glucose Uptake in Red-Type Skeletal Muscle. Toda C, Shiuchi T, Kageyama H, Okamoto S, Coutinho E A, Sato T, Okamatsu-Ogura Y, Yokota S, Takagi K, Tang L, Saito K, Shioda S and Minokoshi Y. Diabetes Mar 2013.


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Effect of vitamin E on alloxan-induced mouse diabetes. Kamimura W, Doi W, Takemoto K, Ishihara K, Wang D-H, Sugiyama H, Oda S, Masuoka N. Clinical Biochemistry, Mar 2013.


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Ablation of Rnf213 retards progression of diabetes in the Akita mouse. Kobayashi H, Yamazaki S, Takashima S, Liu W, Okuda H, Yan J, Fujii Y, Hitomi T, Harada K H, Habu T, Koizumi A. Biochemical and Biophysical Research Communications, Vol.432(3), p519-525, Mar 2013.

 

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Hypothalamic ATF3 is involved in regulating glucose and energy metabolism in mice. Lee Y-S, Sasaki T, Kobayashi M, Kikuchi O, Kim H-J, Yokota-Hashimoto H, Shimpuku M, Susanti V-Y, Ido-Kitamura Y, Kimura K, Inoue H, Tanaka-Okamoto M, Ishizaki H, Miyoshi J, Ohya S, Tanaka Y, Kitajima S, Kitamura T. Diabetologia, Mar 2013.


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Ras-related C3 botulinum toxin substrate 1 (RAC1) regulates glucose-stimulated insulin secretion via modulation of F-actin. S. Asahara, Y. Shibutani, K. Teruyama, H. Y. Inoue, Y. Kawada, H. Etoh, T. Matsuda, M. Kimura-Koyanagi, N. Hashimoto, M. Sakahara, W. Fujimoto, H. Takahashi, S. Ueda, T. Hosooka, T. Satoh, H. Inoue, M. Matsumoto, A. Aiba, M. Kasuga, Y. Kido. Diabetologia, Feb 2013.


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Toll-like receptor 2 and palmitic acid cooperatively contribute to the development of nonalcoholic steatohepatitis through inflammasome activation in mice. Miura K, Yang L, Rooijen N, Brenner D A, Ohnishi H, Seki E. Hepatology, Vol.57(2), p577-589, Feb 2013.


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Transcriptional Regulatory Factor X6 (Rfx6) Increases Gastric Inhibitory Polypeptide (GIP) Expression in Enteroendocrine K-cells and Is Involved in GIP Hypersecretion in High Fat Diet-induced Obesity*. K.Suzuki, N.Harada, S.Yamane, Y.Nakamura, K.Sasaki, D.Nasteska, E.Joo, K.Shibue, T.Harada, A.Hamasaki, K.Toyoda, K.Nagashima and N.Inagaki. The Journal of Biological Chemistry, Vol.288, p1929-1938, Jan 2013.


99.

Improved hypothermic short-term storage of isolated mouse islets by adding serum to preservation solutions. Yasuko Kimura, Teru Okitsu, Liu Xibao, Hiroki Teramae, Atsuhito Okonogi, Kentaro Toyoda, Shinji Uemoto and Masanori Fukushima. Islets, Vol.5(1), Jan 2013.


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Anti-diabetic effect of amorphastilbol through PPARα/γ dual activation in db/db mice. Lee W, Ham J, Kwon H C, Kim Y K, Kim S-N. Biochemical and Biophysical Research Communications, Jan 2013.

101.

Transcriptional Regulatory Factor X6 (Rfx6) Increases Gastric Inhibitory Polypeptide (GIP) Expression in Enteroendocrine K-cells and Is Involved in GIP Hypersecretion in High Fat Diet-induced Obesity. Suzuki K, Harada N, Yamane S, Nakamura Y, Sasaki K, Nasteska D, Joo E, Shibue K, Harada T, Hamasaki A,Toyoda K, Nagashima K and Inagaki N. The Journal of Biological Chemistry, Vol.288, p1929-1938, Jan 2013.


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Beneficial effects of Allium sativum L. stem extract on lipid metabolism and antioxidant status in obese mice fed a high fat diet. Kim I, Kim H-R, Kim J-H, Om A-S. Journal of the Science of Food and Agriculture, 2013.


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Intake of mulberry 1-deoxynojirimycin prevents diet-induced obesity through increases in adiponectin in mice. Tsuduki T, Kikuchi I, Kimura T, Nakagawa K, Miyazawa T. Food Chemistry, Vol.139(14), p16-23, 2013.


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产品编号 产品名称 产品规格 产品等级
634-01481 (AKRIN-011T)LBIS® Insulin-Mouse-T 96 tests

LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型) LBIS® Insulin-Mouse (H type)

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LBIS® Insulin-Mouse (H type)LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Mouse (H type)

LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型)

  胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

  A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含 Zn 离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。


肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点

● 有色缓冲液(蓝色)、容易确认分装后的孔

● 短时间测定(总的反应时间:3小时)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 操作简便,不需要特别的预处理

◆构成

组成部分

状态

容量

(A) 抗体固相化 96 孔板

洗净后使用

96 wells(8×12)/1 块

(B) 胰岛素标准溶液(小鼠)(200 ng/mL

稀释后使用

300 μL/1 瓶

(C) 缓冲液(蓝色)

即用

60 mL/1 瓶

(D) 生物素结合抗胰岛素抗体

稀释后使用

200 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

200 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1 瓶

(H) 反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1 瓶

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1 瓶

封板膜

3 张

使用说明书

1 份

◆样品信息

小鼠的血清、血浆、培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液

 


◆测定范围


0.5~100 ng/mL(标准曲线范围)


◆Validation data

精度测量(检测内变动系数)

 

样品

A

B

C

1

0.749

10.6

81.9

2

0.749

10.7

80.9

3

0.749

10.6

82.3

4

0.711

10.8

82.9

5

0.711

10.8

81.9

mean

0.734

10.7

82.0

SD

0.021

0.11

0.72

CV(%)

2.8

1.0

0.88

单位:ng/mL

 

再现性测试(检测内变动系数)

 

测量日/样品

F

G

H

0

5.61

37.3

78.9

1

5.85

37.9

77.9

2

5.65

37.6

78.2

mean

5.70

37.6

78.3

SD

0.126

0.287

0.544

CV(%)

2.2

0.8

0.7

单位:ng/mL  n=2

 

添加回收测试

 

样品D

 

添加量

实测值

回收量

回收率(%)

0

1.10

1.0

2.16

1.06

106

2.5

3.60

2.50

100

5.1

6.06

4.96

97.3

单位:ng/mL  n=2

 

样品E

 

添加量

实测值

回收量

回收率(%)

0

31.5

20

51.5

20.0

100

40

73.1

41.6

104

60

95.1

63.6

106

单位:ng/mL n=2

 

 

稀释直线性测试

 

用稀释缓冲液分4次连续稀释2个血清样品的测量结果,直线回归方程的R20.9997~1.0之间。

相关资料


LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Mouse (H type) LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Mouse (H type) LBIS® 小鼠胰岛素 ELISA 试剂盒(H 型)                              LBIS® Insulin-Mouse (H type)
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

参考文献

1.

Does a Treadmill Running Exercise Contribute to Preventing Deterioration of Bone Mineral Density and Bone Quality of the Femur in KK-Ay Mice, a Type 2 Diabetic Animal Model? Takagi S, Yamashita T, Miura T. Calcif Tissue Int. 2017 Aug 4. 


2.

Further characterization of diabetes mellitus and body weight loss in males of the congenic mouse strain DDD. Cg-Ay. Suto J, Satou K. The Journal of Veterinary Medical Science, 2015.


3.

Fat and carbohydrate in western diet contribute differently to hepatic lipid accumulation. Wu W, Tsuchida H, Kato T, Niwa H, Horikawa Y, Takeda J, Iizuka K. Biochem Biophys Res Commun. Vol.461(4), p681-6, Jun 2015.


4.

C-C Chemokine Receptor 2 Inhibitor Ameliorates Hepatic Steatosis by Improving ER Stress and Inflammation in a Type 2 Diabetic Mouse Model. Kim HM, Lee ES, Lee BR, Yadav D, Kim YM, Ko HJ, Park KS, Lee EY, Chung CH. PLoS One. 2015 Mar 27;10(3):e0120711.


5.

Viability and functional assessment of murine pancreatic islets after transportation between Korea and Japan. Lee S, Takahashi Y, Lee KM, Mizuno M, Nemeno JG, Takebe T, Lee JI. Transplant Proc. Vol.47(3), p738-41, Apr 2015.


6.

Calorie restriction-mediated restoration of hypothalamic signal transducer and activator of transcription 3 (STAT3) phosphorylation is not effective for lowering the body weight set point in IRS-2 knockout obese mice. Satoko Senda,  Atsushi Inoue,  Arshad Mahmood,  Ryo Suzuki,  Nozomu Kamei,  Naoto Kubota,  Taku Watanabe,  Masashi Aoyama,  Allah Nawaz,  Yoshiaki Ohkuma,  Koichi Tsuneyama,  Yukiko Koshimizu,  Isao Usui,  Kumiko Saeki,  Takashi Kadowaki,  Kazuyuki Tobe. Diabetology International February 2015


7.

Overweight in Mice and Enhanced Adipogenesis In Vitro are Associated with Lack of the Hedgehog Coreceptor Boc. Lee HJ, Jo SB, Romer AI, Lim HJ, Kim MJ, Koo SH, Krauss RS, Kang JS. Diabetes. 2015 Jan 9.


8.

Investigating the suspension culture on aggregation and function of mouse pancreatic β-cellsK.-C.Yang, C.-C.Wu, S.-H.Yang, C.-C.Chiu, S.Sumi, H.-S. Lee. Journal of Biomedical Materials Research Part A, Vol.101A(8), p2273-2282, Aug 2013.


9.

Microenvironment-regulated gene expression, morphology, and in vivo performance of mouse pancreatic β-cells. Chen P-Y., Wu C-C., Lu D-H., Sumi S., Lin F-H., Yange K-C. Process Biochemistry, Vol.48(1), p58-67, Jan 2013.


10.

The anti-ulcer agent, irsogladine, increases insulin secretion by MIN6 cells. T.Matsumoto,K.Sakurai, A.Tanaka, T.Ishibashi, K.Tachibana, K.Ishikawa, K.Yokote. European Journal of Pharmacology, Vol.685(1-3), p213-217, Jun 2012.


11.

Cell coupling regulates Ins1, Pdx-1 and MafA to promote insulin secretion in mouse pancreatic beta cells. K.-C. Yanga., Z. Qi., G. Yanai., Y. Shirouza., D.-H. Lu., H.-S. Lee., S. Sumi. Process Biochemistry, Vol.46(9), p1853-1860, 2011.


12.

Dietary Combination of Fish Oil and Taurine Decreases Fat Accumulation and Ameliorates Blood Glucose Levels in Type 2 Diabetic/Obese KK-Ay Mice. N. Mikami., M. Hosokawa., K. Miyashita. Journal of Food Science, Vol. 77(6), pH114-H120, Jun 2012.


13.

Cell coupling regulates Ins1, Pdx-1 and MafA to promote insulin secretion in mouse pancreatic beta cells. K.C. Yang., Z. Qi., G. Yanai., Y. Shirouza., D.H. Lu., H.S. Lee., and S. Sumi. Process Biochemistry.


产品编号 产品名称 产品规格 产品等级
634-10379 (AKRIN-011H)LBIS® Mouse Insulin ELISA Kit(H-type)
LBIS® 小鼠胰岛素 ELISA试剂盒(H型)
96 tests

LBIS® 猪胰岛素 ELISA 试剂盒 LBIS® Insulin-Porcine

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

LBIS® Insulin-PorcineLBIS® 猪胰岛素 ELISA 试剂盒                              LBIS® Insulin-Porcine

LBIS® 猪胰岛素 ELISA 试剂盒

胰岛素是由胰脏内的胰岛β细胞分泌,分子量约 5800,等电点在 5.4 左右的一种蛋白质激素。

A6-A11、A7-B7、A20-B-19 之间形成二硫键,在酸性溶液或者不含 Zn 离子的中性水溶液中形成二聚体,在含锌离子的中性溶液中,则形成含2个 Zn 离子的六聚体。

肝脏、肌肉、脂肪组织是主要的靶组织,分别有以下的作用。

肝脏:促进糖原、蛋白质、脂肪酸合成、促进糖类的摄取和利用、抑制糖异生。

肌肉:糖类、氨基酸、K细胞膜通透性增大、促进糖原、蛋白质的合成、抑制蛋白质分解。

脂肪组织:葡萄糖细胞膜通透性增大、促进脂肪酸的合成。

胰岛素是细胞内的合成单链胰岛素原通过二硫键结合一起形成的。在酶分解作用下被激活,C肽和胰岛素分离。

◆特点

● 短时间测定(总的反应时间:3小时)

● 微量样品(标准操作:10 μL)可测

● 使用对环境无害的防腐剂

● 全部试剂均为液体,可直接使用

● 精密的测定精度和高再现性

● 操作简便,不需要特别的预处理

◆构成

组成

状态

容量

(A)   抗体固相化 96 孔板

洗净后使用

96 wells(8×12)/1 块

(B) 胰岛素标准液(猪)(240 ng/mL)

稀释后使用

25 μL/1 瓶

(C) 缓冲液

即用

60 mL/1 瓶

(D) 生物素结合抗胰岛素抗体

稀释后使用

10 μL/1 瓶

(E) 过氧化物・抗生物素蛋白结合物

稀释后使用

20 μL/1 瓶

(F) 显色液(TMB)

即用

12 mL/1

(H) 反应终止液(1M H2SO4)※小心轻放

即用

12 mL/1

( I ) 浓缩洗净液(10×)

稀释后使用

100 mL/1瓶

封板膜

3 张

使用说明书

1 份

◆样品信息

猪的血清•血浆•培养液

10 μL/well(标准操作)

※血浆采血建议使用肝素处理血液

 

 

◆测定范围

0.188~12 ng/mL(标准曲线范围)

◆Validation data

精度测试(检测内变动系数)

样品

A

B

C

mean

0.991

0.482

0.201

SD

0.0321

0.0175

0.0099

CV(%)

3.2

3.6

4.9

单位:ng/mL,n=5

再现性测试(检测内变动系数)

测量日/样品

D

E

F

mean

1.452

0.901

0.346

SD

0.0562

0.0321

0.0162

CV(%)

3.9

3.6

4.7

3天内 单位:ng/mL,n=2

添加回收测试


样品G

添加量

实测值

回收量

回收率(%)

0.343

0.25

0.576

0.233

93.2

0.5

0.802

0.459

91.7

1

1.295

0.952

95.2

2

2.301

1.958

97.9

单位:ng/mL

样品H

添加量

实测值

回收量

回收率(%)

0.202

0.25

0.437

0.235

93.8

0.5

0.666

0.464

92.8

1

1.201

0.999

99.9

2

2.240

2.038

102

单位:ng/mL

相关资料


LBIS® 猪胰岛素 ELISA 试剂盒                              LBIS® Insulin-Porcine LBIS® 猪胰岛素 ELISA 试剂盒                              LBIS® Insulin-Porcine LBIS® 猪胰岛素 ELISA 试剂盒                              LBIS® Insulin-Porcine
说明书

ELISA试剂盒选择指南①②

ELISA试剂盒选择指③④

产品编号 产品名称 产品规格 产品等级
630-01461 (AKRIN-013T)LBIS® Insulin-Porcine 96 tests

NS补充剂(不含胰岛素) 神经细胞培养用无血清补充剂

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

神经细胞培养用无血清补充剂NS补充剂(不含胰岛素)                              神经细胞培养用无血清补充剂

NS补充剂(不含胰岛素)



  本产品是神经细胞培养用的不含血清的补充剂。可用于研究胰岛素分泌和胰岛素受体。

 


◆数据


大鼠大脑皮质来源原代神经细胞的培养


NS补充剂(不含胰岛素)                              神经细胞培养用无血清补充剂

  将从大鼠胎儿大脑皮层(E17)提取出来的神经细胞在NS基础培养基和本产品或NS补充剂(含胰岛素的产品)(NSS)混合的培养基中培养,确认培养第6天的相对细胞数(以在含有NSS的培养基中培养时的细胞数为1)。在作为比较对象的本产品中添加与普通NSS所含胰岛素浓度的0.25倍、1倍的胰岛素,其添加条件相同。结果表明,由于胰岛素具有促进神经细胞生长的作用,本产品与普通的NSS相比活细胞数量虽比较低,但是加入胰岛素时,可确认与普通的NSS显示的细胞数量相同。



◆产品列表

产品编号

产品名称

规格

包装

149-09721

NS Supplement without Insulin(×50)
不含胰岛素的NS补充剂(×50)

细胞培养用

10 mL

145-09723

50 mL



◆相关产品


产品编号

产品名称

规格

包装

148-09615

NS Basal Medium
NS基础培养基

细胞培养用

500 mL

146-09351

NS Supplement(×50)
NS 补充剂(×50)

细胞培养用

10 mL

142-09691

NS Supplement without Vitamin A(×50)
NS 补充剂不含维生素A (×50)

细胞培养用

10 mL

141-09041

N2 Supplement with Transferrin(Apo)(×100)
N2神经细胞生长添加剂含转铁蛋白(Apo)(×100)

细胞培养用

5 mL

141-08941

N2 Supplement with Transferrin(Holo)(×100)
N2神经细胞生长添加剂含转铁蛋白(Holo)(×100)

细胞培养用

5 mL

※ 本页面产品仅供研究用,研究以外不可使用。

产品编号 产品名称 产品规格 产品等级