PCAF (E-8) 抗体 (琼脂糖偶联) PCAF (E-8) AC

PCAF (E-8) 抗体 (琼脂糖偶联)

PCAF (E-8) AC

详细描述:
In the intact cell, DNA closely associates with histones and other nuclear proteins to form chromatin. The remodeling of chromatin is believed to be a critical component of transcriptional regulation and a major source of this remodeling is brought about

应用范围:WB, IP, IF, IHC(P), ELISA; 反应种属:m, r, h; Isotype:mouse monoclonal IgG1; 标记:Agarose。

货号 产品名称 品牌 购买
货号 名称 单位 购买
sc-13124 AC PCAF (E-8) 抗体 (琼脂糖偶联) 500 µg/ml, 25% ag 咨询客服

细胞器检测试剂盒

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

细胞器检测试剂盒

细胞器检测试剂盒


Enzo 为细胞器特异性染色试验提供多种颜色的荧光,可用于荧光显微镜或共聚焦显微镜进行荧光共定位分析研究和检测化学物质或环境压力对细胞结构的改变。



◆三种细胞器同时检测试剂盒

Organelle-ID RGB® III assay Kit – ENZ-51032
    

预混的细胞器特异性染料可用于多重检测:内质网、高尔基体和细胞核。


细胞器检测试剂盒

 

特点


● 包含三种染料

● 光感度高,不易淬灭



工作原理


  预混的细胞器特异性染料可用于多重检测:内质网(红色)、高尔基体(绿)和细胞核(蓝)。DNA 染色试剂盒 NUCLEAR-ID®  Red DNA stain(for fluorescence microscopy and flow cytometry)

  高亮度具有细胞通透性的 DNA 染料。


细胞器检测试剂盒

 


特点


● 低浓度和低细胞毒性可得到高亮度结果
● 无光致漂白效应
● 无需 RNA 酶处理
● 远红外荧光特异性 DNA 染料无需紫外光源



◆溶酶体积聚检测试剂盒

Lyso-ID® Red cytotoxicity kit (GFP-Certified® ) for microplates –  ENZ-51015


    活细胞毒性检测试剂盒,无需细胞固定或破膜操作

细胞器检测试剂盒

 

特点


● Lyso-ID® 染料快速进入细胞,标记酸性细胞器

● 市面上唯一一款可以长期检测细胞毒性的试剂盒
● 与其它 GFP 绿色荧光探针兼容



工作原理


阳离子两性示踪剂(CAT)染料快速进入细胞,在溶酶体和弱酸性的类溶酶体小泡中发红色荧光。

分类

产品编号

Cellestial产品

应用

细胞类型

染料激发/发射波长(nm)

FC

MC

MP

L

F

P

细胞器检测

ENZ-51025-K500

ER-ID® Green Assay Kit
ER-ID® 内质网检测试剂盒(绿色)

441/551

ENZ-51026-K500

ER-ID® Red Assay Kit (GFP-Certified)
ER-ID® 胞内质网检测试剂盒(红色)(GFP-Certified)

580/677

ENZ-51028-K100

Golgi-ID® Green Assay Kit
Golgi-ID® 高尔基体检测试剂盒(绿色)

473/534

ENZ-51034-K500

Lyso-ID® Green Detection Kit
Lyso-ID® 溶酶体检测试剂盒(绿色)

Lyso-ID Green 481/544
Hoechst 33342 (nuclear) 350/461

ENZ-51005-500

Lyso-ID® Red Detection Kit (GFP-Certified)
Lyso-ID® 溶酶体检测试剂盒(红色)(GFP-Certified)

Lyso-ID Red 568/667
  Hoechst  33342 (nuclear) 350/461

ENZ-51015-KP002

Lyso-ID® Red Cytoxicity Kit (GFP-Certified)
Lyso-ID® 溶酶体细胞毒性检测试剂盒(红色) (GFP-Certified)

568/667

ENZ-51007-500

Mito-ID® Red Detection Kit (GFP-Certified)
Mito-ID® 线粒体检测试剂盒(红色)(GFP-Certified)

Mito-ID Red 558/690
Hoechst 33342 (nuclear) 350/461

ENZ-51022-K500

Mito-ID® Green Detection Kit
Mito-ID® 线粒体检测试剂盒(绿色)

Mito-ID Green 460/560
Hoechst 33342 (nuclear) 350/461

ENZ-52406

Nuclear-ID® Red DNA Stain
Nuclear-ID® 细胞核DNA染色试剂盒(红色)

568/637

ENZ-51009-500

Nucleolar-ID® Green Detection Kit
Nucleolar-ID® 细胞核染色试剂盒(绿色)

450/481

ENZ-51006-500

Total Nuclear-ID ® Green/Red Nucleolar/Nuclear
Total Nuclear-ID ® 核仁/细胞核检测试剂盒(绿色/红色)

Nucleolar-ID   Green 450/481
Nuclear-ID Red 568/631

ENZ-CHM103-0200

Nuclear-ID® Blue DNA stain (GFP-Certified® )
胞Nuclear-ID® 细胞核染色试剂(蓝色)(GFP-Certified®)

350/461

ENZ-53007-C200

Organelle-ID® RGB Reagent I
Organelle-ID® 溶酶体、线粒体和细胞核检测试剂

Lysosome 568/667
Mitochondria 460/560
Nucleus 350/461

ENZ-53008-C200

Organelle-ID® RGB Reagent II
Organelle-ID® 溶酶体、线粒体和细胞核检测试剂

Lysosome 568/667
ER 440/565
Nucleus 350/461

ENZ-51032-K100

Organelle-ID® RGB III Assay Kit
Organelle-ID® 内质网、高尔基体和细胞核检测试剂

ER 580/677
Golgi 473/543
Nucleus 357/449

ENZ-53009-C200

Organelle-ID® RGB Reagent IV
Organelle-ID® 内质网、高尔基体和细胞核检测试剂

ER 580/677
Lysosome 481/544
Nucleus 350/461



相关产品资料请点击下载:活细胞荧光分析 Ver.3

产品编号 产品名称 产品规格 产品等级
ENZ-51025-K500 ER-ID® Green assay kit 
ER-ID® 绿色 检测 试剂盒
1 Kit

Pesticide Mixture Standard Solution PL-12-1 (each 20μg/ml Acetone Solution) 农药混合标准溶液PL-12-1 品牌:Wako


品牌:Wako
CAS No.:
储存条件:-20℃
纯度:
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

161-23941

for Pesticide Residue Analysis 1 ml×5A 咨询


* 干冰运输、大包装及大批量的产品需酌情添加运输费用


* 零售价、促销产品折扣、运输费用、库存情况、产品及包装规格可能因各种原因有所变动,恕不另行通知,确切详情请联系上海金畔生物科技有限公司。

产品描述相关资料下载相关产品浏览记录

农药混标溶液PL-12-1(26种成分,161-23941、167-23943)

Pesticide Mixture Standard Solution PL-12-1 (each 20μg/ml Acetone Solution)                                                      农药混合标准溶液PL-12-1            品牌:Wako


milllipore0.2um尼龙过滤膜47mm直径

详细介绍

milllipore0.2um尼龙过滤膜

圆片膜直径规格:milllipore0.2um尼龙过滤膜47mm直径,13mm直径,25mm直径,90mm直径等

尼龙滤膜与各种溶剂相容。 提供两种滤膜:表面滤膜(GNWP 和 HNWP),孔径为 0.22 和 0.45um; 编织网格膜 (NY…),网格开口为 11 至 180 ?m。

说明: 尼龙表面滤膜,亲水,0.22 um,47 mm,白色,光面

 

详细产品信息可和选购

GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒 GFP-CERTIFIED® Apoptosis/Necrosis detection kit

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒                              GFP-CERTIFIED® Apoptosis/Necrosis detection kit

GFP-CERTIFIED® Apoptosis/Necrosis detection kit

可进行区分正常细胞、早期凋亡细胞、晚期凋亡细胞和坏死细胞的多重检测,可与 GFP 和其他绿色荧光探针兼容。

 

● 可以兼容 GFP 和其他绿色荧光探针

● 容易区分正常细胞、早期凋亡细胞、晚期凋亡细胞和坏死细胞

● 已根据荧光显微镜和流式细胞仪等应用进行过优化

● 适用于死亡途径分析及药物、毒素研究

 

从凋亡到坏死的过渡是一个松散定义的连续体。质膜细胞外表面上磷脂酰丝氨酸(PS)的暴露仍是早期细胞凋亡的共同标志。这时候在Ca2+存在下,磷脂结合蛋白例如 Annexin V 与 PS 具有亲和力。由于 Annexin V 不具有细胞渗透性,所以这种胞外PS的结合是早期凋亡细胞对具有选择性的。

同样,质膜完整性的丧失,如不具有膜渗透性DNA嵌入染料若能标记出细胞核,则是表明晚期细胞凋亡和坏死的直接方法。考虑到Annexin V通常与荧光素(又称FITC)偶联,检测绿色荧光蛋白(GFP)表达细胞中的凋亡时可能会出现问题。以上两个荧光团的发射图谱会发生光谱重叠,使信号之间的区分变得困难或不可能,从而损害了总体上的数据质量。GFP-CERTIFIED® 细胞凋亡/坏死检测系统专为表达GFP的细胞系以及表达蓝色或青色荧光蛋白(BFP、CFPs)的细胞而设计,同时也可以应用于不带荧光蛋白的细胞的凋亡和坏死的细胞。另外,本试剂盒适合用于活细胞或结合了探针(如标记抗体、或与荧光素或香豆素显示相似光谱特性的其他荧光偶联物)的细胞。本试剂盒包含了用于确定细胞凋亡及坏死的早期和晚期阶段中所需的全部试剂。Annexin V -EnzoGold(增强型Cyanine-3)偶联物能够检测不同于荧光素或GFP的细胞凋亡。坏死检测试剂(红色)类似于发出红色的染料7-AAD,可促进晚期细胞凋亡和坏死检测。本试剂盒还包含了可用作阳性对照的凋亡诱导剂(Staurosporine)。检测试剂可单独使用或分别与其他单独或多重应用组合使用。本试剂盒还可以通过流式细胞仪和荧光/共焦显微镜提供快速、准确的检查结果。

GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒                              GFP-CERTIFIED® Apoptosis/Necrosis detection kit

GFP、Annexin V-Cyanine 3 偶联物和坏死检测试剂(红色)的激发(阴影线)和发光(固体)光谱。

三种染料都可以轻易地被 488 nm 激光源激发。所有荧光团之间的发射峰值容易区分。

GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒                              GFP-CERTIFIED® Apoptosis/Necrosis detection kit

GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒(ENZ-51002



GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒                              GFP-CERTIFIED® Apoptosis/Necrosis detection kit


流式细胞仪。用0.2%DMSO(panel A)模拟诱导 Jurkat 细胞,或用 2 μM 星形孢菌素(panel B)在37°C下诱导 Jurkat 细胞4h。经过处理后,在含有 Annexin V-Cyanine 3 和坏死检测试剂(红色;一种远红色发光的 DNA 嵌入染料)的缓冲液中孵育细胞,然后用 488 nm 激光的流式细胞仪进行分析,用 FL2(细胞凋亡)和 FL3(坏死)通道进行荧光检测。

模拟诱导的细胞凋亡和坏死主要呈阴性。处理4h 后,会出现3种细胞群:

(1)可以存活且不凋亡、不坏死的细胞(Annexin V-Cyanine 3、坏死检测试剂呈阴性);

(2)正在经历凋亡的细胞(Annexin V-Cyanine 3 呈阳性和 NDR 呈阴性);

(3)处于晚期凋亡和早期坏死的细胞(Annexin V-Cyanine 3 和坏死检测试剂呈阳性)。

 


GFP-CERTIFIED® 细胞凋亡/坏死检测试剂盒                              GFP-CERTIFIED® Apoptosis/Necrosis detection kit

用 2.5 µM 星形孢菌素刺激 Jurkat 细胞 0-6 h。使用 Jurkat 悬浮细胞的流式细胞仪结果表现为早期凋亡(Annexin V-EnzoGold)和晚期凋亡/坏死(Annexin V-EnzoGold 和坏死染色)。



◆产品规格


 应用:

 流式细胞仪、荧光显微镜、荧光检测。

 使用事项/稳定性:

 Annexin V-EnzoGold 和结合缓冲液应在4°C储存。
 其他全部试剂应在-20°C储存。
 重组诱导剂(星形孢菌素)应在-20°C下储存。具体请参阅说明书。

 储存条件:

 避光。

 运输:

 蓝冰运输。

 短期储存温度:

 4°C

 试剂盒构成:

 凋亡检测试剂 (Annexin   V-EnzoGold)
 坏死检测试剂
 凋亡诱导剂(Staurosporine)
 结合缓冲液(10X)

 技术信息/产品说明:

 应用说明:
 Image-Based Analysis of a Human Neurosphere Stem Cell Model for the Evaluation of Potential 

 Neurotoxicants
 引用样本:
 For an overview on cited samples please click here.

 监管状况:

 RUO-仅供研究用



点击下载此处下载相关产品宣传页

 其他自噬相关产品



  自噬抑制剂

 

产品编号

产品名称

应用

规格

BML-AP502-0025

3-Methyladenine

3-甲基腺嘌呤,PI3激酶抑制剂

25 mg

BML-CM110-0100

Bafilomycin A1

巴伐洛霉素,ATPase抑制剂

100 μg

 

 

自噬激活剂

 

产品编号

产品名称

应用

规格

产品编号

产品名称

BML-PE180-0001

Thapsigargin

毒胡萝卜素,ATPase抑制剂

1 mg

BML-PE180-0001

Thapsigargin

BML-CC104-0010

Tunicamycin

衣霉素,GlcNAc磷酸转移酶抑制剂

10 mg

BML-CC104-0010

Tunicamycin

ALX-550-084-G005

Carbamazepine

卡马西平,镇痉剂和止痛剂

5 g

ALX-550-084-G005

Carbamazepine

BML-SL100-0005

C2 Ceramide

C2-神经酰胺,细胞渗透性神经酰胺类似

5 mg

BML-SL100-0005

C2 Ceramide

BML-A275-0005

Rapamycin

雷帕霉素,免疫抑制剂

5 mg

BML-A275-0005

Rapamycin

BML-CA409-0050

Xestospongin C

IP3受体抑制剂

50 μg

BML-CA409-0050

Xestospongin C

 

 

自噬化合物库 

 

产品编号

产品名称

应用

规格

BML-AP502-0025

3-Methyladenine

3-甲基腺嘌呤,PI3激酶抑制剂

25 mg

BML-CM110-0100

Bafilomycin A1

巴伐洛霉素,ATPase抑制剂

100 μg

参考文献


 1.

Inhibitory role of TRIP-Br1/XIAP in necroptosis under nutrient/serum starvation: Z. Sandag, et al.; Mol. Cells 43, 236 (2020), 摘要全文

 2.

Inhibitory role of AMP‑activated protein kinase in necroptosis of HCT116 colon cancer cells with p53 null mutation under nutrient starvation: D.T. Le, et al.; Int. J. Oncol. 54, 702 (2019), 摘要;


 3.

Injectable and Quadruple-Functional Hydrogel as an Alternative to Intravenous Delivery for Enhanced Tumor Targeting: Z.Q. Zhang, et al.; ACS Appl. Mater. Interfaces 11, 34634 (2019), 摘要;


 4.

Intrinsic antibacterial activity of nanoparticles made of β-cyclodextrins potentiates their effect as drug nanocarriers against tuberculosis: A. Machelart, et al.; ACS Nano 13, 3992 (2019), 摘要;


 5.

Knockdown of TM9SF4 boosts ER stress to trigger cell death of chemoresistant breast cancer cells: Y. Zhu, et al.; Oncogene 38, 5778 (2019), Application(s): Flow cytometry using MCF-7 cells, 摘要;


  6.

PKM2 coordinates glycolysis with mitochondrial fusion and oxidative phosphorylation: T. Li, et al.; Protein Cell 10, 583 (2019), Application(s): Flow cytometry using H1299 and HepG2 cells, 摘要;

 

 7.

Tamoxifen acts on Trypanosoma cruzi sphingolipid pathway triggering an apoptotic death process: M. Landoni, et al.; Biochem. Biophys. Res. Commun. 516, 934 (2019), 摘要;

 

 8.

Anti-leukemic efficacy of BET inhibitor in a preclinical mouse model of MLL-AF4+ infant ALL: M. Bardini, et al.; Mol. Cancer Ther. 17, 1705 (2018), 摘要;

 

 9.

Pivotal role of human stearoyl-CoA desaturases (SCD1 and 5) in breast cancer progression: oleic acid-based effect of SCD1 on cell migration and a novel pro-cell survival role for SCD5: C. Angelucci, et al.; Oncotarget. 9, 24364 (2018), Application(s): Fluorescent microscopy with MCF-7 cells, 摘要全文

 

10.

Preclinical efficacy and safety of CD19CAR cytokine-induced killer cells transfected with Sleeping Beauty transposon for the treatment of acute lymphoblastic leukemia: C.F. Magnani, et al.; Hum. Gene. Ther. 29, 605 (2018), 摘要;


11.

Protective effect of a newly developed fucose-deficient recombinant antithrombin against histone-induced endothelial damage: T. Iba, et al.; Int. J. Hematol. 107, 528 (2018), 摘要;


12.

The poly (ADP-ribose) polymerase inhibitor olaparib induces up-regulation of death receptors in primary acute myeloid leukemia blasts by NF-κB activation: I. Faraoni, et al.; Cancer Lett. 423, 127 (2018), Application(s): Flow cytometry with primary AML cells, 摘要;


13.

Toxicity and phototoxicity in human ARPE-19 retinal pigment epithelium cells of dyes commonly used in retinal surgery: D. Awad, et al.; Eur. J. Ophthalmol. 28, 433 (2018), 摘要全文


14.

Cluster microRNAs miR‐194 and miR‐215 suppress the tumorigenicity of intestinal tumor organoids: T. Nakaoka, et al.; Cancer Sci. 108, 678 (2017), Application(s): Flow cytometry using organoid culture of mouse intestinal tumors, 摘要

15.

Elaidic Acid, a Trans-Fatty Acid, Enhances the Metastasis of Colorectal Cancer Cells: H. Ohmori, et al.; Pathobiology 84, 144 (2017), 摘要;


16.

Metabolic modulation of Ewing sarcoma cells inhibits tumor growth and stem cell properties: A. Dasgupta, et al.; Oncotarget. 8, 77292 (2017), Application(s): Flow cytometry with A673 cells, 摘要全文


17.

Multiple hyperthermia-mediated release of TRAIL/SPION nanocomplex from thermosensitive polymeric hydrogels for combination cancer therapy: Z.Q. Zhang, et al.; Biomaterials. 132, 16 (2017), Application(s): Confocal microscopy with PC3 and U-87 MG cells, 摘要;


18.

Pro-metastatic intracellular signaling of the elaidic trans fatty acid: K. Fujii, et al.; Int. J. Oncol. 50, 85 (2017), 摘要;


19.

Visualization of ceramide channels in lysosomes following endogenous palmitoyl-ceramide accumulation as an initial step in the induction of necrosis: M. Yamane, et al.; Biochem. Biophys. Rep. 11, 174 (2017), Application(s): Confocal microscopy with A549 cells, 摘要全文


20.

Immunotherapy of acute leukemia by chimeric antigen receptor-modified lymphocytes using an improved Sleeping Beauty transposon platform: C.F. Magnani, et al.; Oncotarget 7, 51581 (2016), Application(s): Flow cytometry using KG-1, REH, Nalm-6, and THP-1 cells, 摘要全文


21.

Novel long chain fatty acid derivatives of quercetin-3-O-glucoside reduce cytotoxicity induced by cigarette smoke toxicants in human fetal lung fibroblasts: N. Sumudu, et al.; Eur. J. Pharmacol. 781, 128 (2016), 摘要;


22.

Phlorofucofuroeckol Improves Glutamate-Induced Neurotoxicity through Modulation of Oxidative Stress-Mediated Mitochondrial Dysfunction in PC12 Cells: J.J. Kim, et al.; PLoS One 11, e0163433 (2016), 摘要全文


23.

PKLR promotes colorectal cancer liver colonization through induction of glutathione synthesis: A. Nguyen, et al.; J. Clin. Invest. 126, 681 (2016), Application(s): Assessed Apoptosis, Flow cytometry, 摘要

24.

Protective effects of β‐casofensin, a bioactive peptide from bovine β‐casein, against indomethacin‐induced intestinal lesions in rats: C. Bessette, et al.; Mol. Nutr. Food Res. 60, 823 (2016), 摘要;


25.

BRCA1, PARP1 and γH2AX in acute myeloid leukemia: Role as biomarkers of response to the PARP inhibitor olaparib: I. Faraoni, et al.; Biochim. Biophys. Acta 1852, 462 (2015), Application(s): Flow cytometry using primary AML cells, 摘要;


26.

Growth-promoting and tumourigenic activity of c-Myc is suppressed by Hhex: V. Marfil, et al.; Oncogene 34, 3011 (2015), Application(s): Flow cytometry using HO15.19 and TGR-1 cells, 摘要;


27.

common set of proteins modulated in Chikungunya virus infection: R. Abraham, et al.; J. Proteomics. 120, 126 (2015), Application(s): Flow cytometry using HEK293 cells, 摘要;


28.

Identification of novel osteogenic compounds by an ex-vivo sp7: luciferase zebrafish scale assay: E. de Vrieze, et al.; Blood 74, 106 (2015), Application(s): Fluorescence microscopy using fish scales, 摘要;


29.

Impaired oxidative phosphorylation regulates necroptosis in human lung epithelial cells: M.J. Koo, et al.; Biochem. Biophys. Res. Commun. 464, 875 (2015), Application(s): Apoptosis/necrosis assay, 摘要;


30.

Influenza virus M2 targets cystic fibrosis transmembrane conductance regulator for lysosomal degradation during viral infection: J.D. Londino, et al.; FASEB J. 29, 2712 (2015), Application(s): Flow cytometry using HEK293 cells, 摘要

31.

Inhibition of autophagy exerts anti-colon cancer effects via apoptosis induced by p53 activation and ER stress: K. Sakitani, et al.; BMC Cancer 15, 795 (2015), Application(s): Flow cytometric analysis of apoptosis, 摘要全文


32.

N-terminal functional domain of Gasdermin A3 regulates mitochondrial homeostasis via mitochondrial targeting: P.H. Lin, et al.; J. Biomed. Sci. 22, 44 (2015), Application(s): Fluorescence microscopy using HaCaT and HEK293 cells, 摘要全文

 

33.

Novel carbocyclic curcumin analog CUR3d modulates genes involved in multiple apoptosis pathways in human hepatocellular carcinoma cells.: K.S. Bhullar, et al. ; Chem. Biol. Interact. 242, 107 (2015), Application(s): Fluorescence microscopy, 摘要;


34.

NPD1-mediated stereoselective regulation of BIRC3 expression through cREL is decisive for neural cell survival: J.M. Calandria, et al.; Cell Death Differ. 22, 1363 (2015), Application(s): Assay, 摘要;


35.

ROS-induced oxidative stress and apoptosis-like event directly affect the cell viability of cryopreserved embryogenic callus in Agapanthus praecox: D. Zhang, et al.; Plant Cell Rep. 34, 1499 (2015), 摘要;

 

36.

The Adhesion GPCR CD97/ADGRE5 inhibits apoptosis: C.C. Hsiao, et al.; Int. J. Biochem. Cell. Biol. 65, 197 (2015), Application(s): Flow cytometry using HT1080 cells, 摘要;


37.

The effect of plasma-derived activated protein C on leukocyte cell-death and vascular endothelial damage: T. Iba, et al.; Thromb. Res 135, 963 (2015), Application(s): Fluorescence Microscopy using leukocytes, 摘要;


38.

Accumulation of cytosolic calcium induces necroptotic cell death in human neuroblastoma: M. Nomura, et al.; Cancer Res. 74, 1056 (2014), 摘要;


39.

Apoptotic and inhibitory effects on cell proliferation of hepatocellular carcinoma HepG2 cells by methanol leaf extract of Costus speciosus: S.V. Nair, et al.; Biomed. Res. Int. 2014, Article ID 637098 (2014), Application(s): Measurement by flow cytometry, 摘要全文


40.

Combination of antithrombin and recombinant thrombomodulin modulates neutrophil cell-death and decreases circulating DAMPs levels in endotoxemic rats: T. Iba, et al.; Throm. Res. 134, 169 (2014), Application(s): Detection Kit using live cells, 摘要;


41.

Fatty acid esters of ohloridzin induce apoptosis of human liver cancer cells through altered gene expression: S.V. Nair, et al.; PLoS One 9, e107149 (2014), Application(s): Fluorescence microscopy of HepG2 cells, 摘要全文


42.

Flavonoid-enriched apple fraction AF4 induces cell cycle arrest, DNA topoisomerase II inhibition, and apoptosis in human liver cancer HepG2 cells: S. Sudan, et al.; Nutr. Cancer 66, 1237 (2014), 摘要;


43.

Quercetin-3-O-glucoside induces human DNA topoisomerase II inhibition, cell cycle arrest and apoptosis in hepatocellular carcinoma cells: S. Sudan, et al.; Anticancer Res. 34, 1691 (2014), 摘要;


44.

A light-activated NO donor attenuates anchorage independent growth of cancer cells: Important role of a cross talk between NO and other reactive oxygen species: S. Sen, et al.; Arch. Biochem. Biophys. 540, 33 (2013), Application(s): Detection Kit using live cells, 摘要;


45.

Alu Elements in ANRIL Non-Coding RNA at Chromosome 9p21 Modulate Atherogenic Cell Functions through Trans-Regulation of Gene Networks: L.M. Holdt, et al.; PLoS Genet. 9, e1003588 (2013), Application(s): Detection Kit using live cells, 摘要

46.

Analysis of protein translocation into the endoplasmic reticulum of human cells: J. Dudek, et al.; Methods Mol. Biol. 1033, 285 (2013), 摘要;


47.

Characterizing virulence-specific perturbations in the mitochondrial function of macrophages infected with Mycobacterium tuberculosis: S. Jamwal, et al.; Sci. Rep. 3, 1328 (2013), 摘要

48.

Evaluation of anticancer effects and enhanced doxorubicin cytotoxicity of xanthine derivatives using canine hemangiosarcoma cell lines: T. Motegi, et al.; Res. Vet. Sci. 95, 600 (2013), Application(s): Fluorescence microscopy using canine HAS cells, 摘要;


49.

Genista sessilifolia DC. extracts induce apoptosis across a range of cancer cell lines: P. Bontempo, et al.; Cell Prolif. 46, 183 (2013), Application(s): Detection Kit using live cells, 摘要;


50.

High mobility group box 1 released from necrotic cells enhances regrowth and metastasis of cancer cells that have survived chemotherapy: Y. Luo, et al.; Eur. J. Cancer. 49, 741 (2013), Application(s): Fluorescence microscopy using CT26 cells, 摘要;


51.

Influence of gefitinib and erlotinib on apoptosis and c-MYC expression in H23 lung cancer cells: M. Suenaga, et al.; Anticancer Res. 33, 1547 (2013), 摘要;


52.

Comparison of different suicide-gene strategies for the safety improvement of genetically manipulated T cells: V. Marin, et al.; Hum. Gene Ther. Methods 23, 376 (2012), Application(s): Flow cytometry using EBV-CTL and 293 T cells, 摘要全文


53.

Maintenance of higher H2O2 levels, and its mechanism of action to induce growth in breast cancer cells: Important roles of bioactive catalase and PP2A: S. Sen, et al.; Free Radic. Biol. Med. 53, 1541 (2012), Application(s): Detection Kit using live cells, 摘要;


54.

Mesenchymal stem cells from Shwachman–Diamond syndrome patients display normal functions and do not contribute to hematological defects: V. André, et al.; Blood Cancer J. 2, e94 (2012), Application(s): Flow cytometry using human neutrophils, 摘要

55.

Methionine excess in diet induces acute lethal hepatitis in mice lacking cystathionine γ-lyase, an animal model of cystathioninuria: H. Yamada, et al.; Free Radic. Biol. Med. 52, 1716 (2012), Application(s): Fluorescence microscopy using mouse hepatocytes, 摘要;


56.

Molecular mechanism of interleukin-2-induced mucosal homeostasis : J. Mishra, et al.; Am. J. Physiol. Cell Physiol. 302, C735 (2012), Application(s): Detection Kit using live cells, 摘要全文


57.

Serratia marcescens induces apoptotic cell death in host immune cells via a lipopolysaccharide- and flagella-dependent mechanism: K. Ishii, et al.; J. Biol. Chem. 287, 36582 (2012), Application(s): Apoptosis detected in Silkworm larvae, 摘要;


58.

Serratia marcescens Induces Apoptotic Cell Death in Host Immune Cells via a Lipopolysaccharide- and Flagella-dependent Mechanism: K. Ishii, et al.; J. Biol. Chem. 287, 36582 (2012), Application(s): Detection Kit using live cells, 摘要全文


59.

Two mutations impair the stability and function of ubiquitin-activating enzyme (E1): T. Lao, et al.; J. Cell. Physiol. 227, 1561 (2012), Application(s): Viability and induction of cell death observed by confocal microscopy, 摘要全文


60.

Critical roles of Cold Shock Domain Protein A as an endogenous angiogenesis inhibitor in skeletal muscle: Y. Saito, et al.; Antioxid. Redox. Signal. 15, 2109 (2011), 摘要;


61.

Cell Surface Externalization of Annexin A1 as a Failsafe Mechanism Preventing Inflammatory Responses during Secondary Necrosis: K.E. Blume, et al.; J. Immunol. 183, 8138 (2009), 摘要全文


62. 

Supplemental Information for: Cell Surface Externalization of Annexin A1 as a Failsafe Mechanism Preventing Inflammatory Responses during Secondary Necrosis: K.E. Blume, et al.; J. Immunol. 183, (2009), (Supplemental Information), 全文

产品编号 产品名称 产品规格 产品等级
ENZ-51002-25 GFP-CERTIFIED® Apoptosis/Necrosis detection kit
细胞凋亡/坏死检测试剂盒(荧光显微镜&流式)(GFP细胞系)
25 assays
ENZ-51002-100 GFP-CERTIFIED® Apoptosis/Necrosis detection kit
细胞凋亡/坏死检测试剂盒(荧光显微镜&流式)(GFP细胞系)
100 assays

细胞周期检测试剂盒

  • 产品特性
  • 相关资料
  • Q&A
  • 参考文献

细胞周期检测试剂盒细胞周期检测试剂盒

Enzo Life Sciences的CELLESTIAL® 系列产品涵盖了广泛应用于活细胞分析的荧光分子探针,用于要求严格的成像应用,如共聚焦显微镜、流式细胞仪和高内涵筛选(HCS),具有需要一致性和可重复性。

NUCLEAR-ID® Green (绿色荧光)和GFP-CERTIFIED® NUCLEAR-ID®红色荧光)两款周期分析试剂盒,为通过流式细胞术进行细胞周期进程的诱导和抑制研究提供了一种便捷的方法,且细胞周期检测结果不受培养时间、温度、染料和细胞密度影响。可以用于以下方面:

(1)确定给定样品处于G0/G1,S和G2/M 期细胞的百分比,以及细胞凋亡之前定量亚G1期的百分比;

(2)正常细胞系和表现出多倍性细胞系的活细胞、透性化及固定细胞的 DNA 研究。

本试剂盒可用于约100次的流式细胞仪检测。使用 Nocodazole 诺考达唑处理的细胞作为对照以检测细胞周期动力学的变化。活细胞研究也可应用于细胞 DNA 含量的测定、细胞周期增长模式变化的检测、细胞凋亡监测,以及评估肿瘤细胞变化和抑制基因机制。



NUCLEAR-ID® Green cell cycle kit

ENZ-51014-100

本试剂盒中荧光染料为绿色。不适用于含绿色荧光蛋白或用 FITC 等绿色染料标记的细胞。

 

 应用:流式细胞仪,荧光显微镜检测

 样品类型:正常细胞系和表现出多倍性细胞系,活细胞、透性化细胞及固定细胞均可

 储存温度: -20°C短期保存,-80°C长期保存

 试剂盒组分:NUCLEAR-ID® Green Cell Cycle Detection Reagent, 100 µL

 试剂盒组分Nocodazole Control, 10 µL

 试剂盒组分10×Assay Buffer, 15 mL

特点


● 染色方法简便,加入染料后直接通过流式细胞仪分析(100 tests)

● 激发光波长 488 nm,发射光波长 530 nm,显示为绿色荧光

● 不需要细胞打孔或 RNA 酶处理

● 结果不受细胞周期培养时间、温度、染料和细胞密度影响

● 从活的或固定细胞中读取 DNA 内容信息

● 监测由药物治疗或其他干扰引起的细胞周期动力学的变化采用大范围的细胞密度进行性能验证

◆NUCLEAR-ID® Red cell cycle kit (GFP-CERTIFIED®)

ENZ-51008-100

本试剂盒中荧光染料为红色。对于含绿色荧光蛋白或用FITC等绿色染料标记的细胞同样适用。

 

● 应用:流式细胞仪,荧光显微镜检测

 样品类型:正常细胞系和表现出多倍性细胞系,活细胞、透性化细胞及固定细胞均可

 储存温度: -20°C短期保存,-80°C长期保存

 试剂盒组分:NUCLEAR-ID® Red Cell Cycle Detection Reagent, 200 µL

 试剂盒组分Nocodazole Control, 10 µL

 试剂盒组分10×Assay Buffer, 15 mL



特点

 可检测活细胞,固定细胞和透化的细胞中 DNA 含量信息的完整试剂盒

 稳定且高纯度的红色荧光染料

 采用不同细胞密度进行性能验证

 无需 RNase 处理

 可检测药物处理或者其他因素引起的细胞周期变化

 无需 UV 激发

 无光漂白效应

 可与其他探针与染料一同使用

 制造严格、消除非特异性检测伪影

 兼容 GFP 绿色荧光蛋白及 FITC



细胞周期检测试剂盒

Figure 1: 使用结构化照明方法,绿色荧光蛋白表达(GFP表达)线粒体和细胞核之间的空间关系的三维重建


细胞周期检测试剂盒

Figure 2: Drug treatments with live cells inhibit cell cycle progression at different phases.

活细胞药物治疗抑制不同阶段的细胞周期进程。


细胞周期检测试剂盒

NUCLEAR-ID® Red DNA Stain 与其他染料的比较

 


实验操作

A. 用NUCLEAR-ID® 红色染料进行细胞染色后,使用流式细胞仪进行细胞周期 DNA 分析


1. 使用(或不使用)实验化合物处理细胞。试管中悬浮细胞液浓度低于5×105 / mL。

2. 选择介质或普通细胞培养缓冲液与 NUCLEAR-ID® 红色 DNA 染色溶液混合。

3. 推荐使用 NUCLEAR-ID® 红色 DNA 染色溶液的250倍至500倍稀释液进行活细胞周期 DNA 分析(终浓度分别为40 μM至20 μM)。

4. 将细胞重悬于 0.5 mL 新稀释的染色溶液中。

5. 轻轻混合后,室温或37℃下孵育15-30分钟。

6. 直接用流式细胞仪分析细胞而无需进一步处理或洗涤。

7. 488 nm 激发激光分析样品使用流式细胞仪 PerCPCy5.5 或 FL3 通道检测。对于 633 nm 激发,选用适当的收集过滤器 > 700 nm,FL4 

      或 FL5,APC-Cy7 通道。

 


B. 经NUCLEAR-ID® 红色染料染色的活细胞用荧光/共聚焦显微镜观察细胞核变化


1. 贴壁细胞:在含有适当培养基的培养皿内的盖玻片上培养贴壁细胞。当细胞达到所需的数量时,小心地除去培养基并稀释到(~100 μL)2000

      至 4000 倍(在选择培养基或缓冲液中)使 NUCLEAR-ID® 红色 DNA 染料能(终浓度分别为 5.0 μM 至 2.5 μM)覆盖到单层细胞。

      悬浮细胞:室温(RT)下以 400× 离心5分钟获得细胞悬浮液。小心吸除上清液,并进行 2000-4000 倍稀释(在选择培养基或缓冲液中)

      使 NUCLEAR-ID® 红色 DNA 染料能够(终浓度分别为 5.0 μM 至 2.5 μM)覆盖到单层细胞。

2. 样品避光保存,并在37°C孵化15-30分钟。

3. 用 100 μL 缓冲液(如 PBS)洗涤细胞。去除多余的缓冲液,将盖玻片放在载玻片上。使用广角荧光或共焦显微镜(推荐放大 60 倍)观察染色

      的细。使用标准罗丹明或德克萨斯红色过滤器集成像系统。

相关产品资料请点击下载:活细胞荧光分析 Ver.3

※ 本页面产品仅供研究用。研究以外不可使用。


相关产品:

NUCLEAR-ID® Red DNA stain

NUCLEAR-ID® DNA 红色染料细胞渗透性 DNA 染色,可广泛应用于高效液相色谱(HPLC)≥93%,流式细胞仪,荧光检测

产品编号 包装
ENZ-51014-100 200 µL

     

参考文献

1.

Growth-promoting and tumorigenic activity of c-Myc is suppressed by Hhex: V. Marfil, et al.; Oncogene 34, 3011 (2015), Abstract;


2.

Epigenetic regulation of planarian stem cells by the SET1/MLL family of histone methyltransferases: A. Hubert, et al.; Epigenetics 8, 79 (2013), Application(s): Cell cycle analysis of stem cells from freshwater planarian by flow cytometry, AbstractFull Text

3.

Gene-specific factors determine mitotic expression and bookmarking via alternate regulatory elements: P. Arampatzi, et al.; Nucleic Acids Res. 41, 2202 (2013), Application(s): Fluorescence imaging of nuclear DNA of human cancer cells, AbstractFull Text

4.

An intact retinoblastoma protein-binding site in Merkel cell polyomavirus large T antigen is required for promoting growth of Merkel cell carcinoma cells: R. Houben, et al.; Int. J. Cancer 130, 847 (2012), Application(s): Cell cycle analysis of cancer cell lines by flow cytometry, AbstractFull Text

5.

Gomisin A enhances tumor necrosis factor-α-induced G1 cell cycle arrest via signal transducer and activator of transcription 1-mediated phosphorylation of retinoblastoma protein: P. Waiwut, et al.; Biol. Pharm. Bull. 35, 1997 (2012), Application(s): Cell cycle analysis of HeLa cells by flow cytometry, AbstractFull Text

6.

A cell-permanent dye for cell cycle analysis by flow and laser-scanning microplatecytometry: Y.J. Xiang, et al.; Nat. Methods 6, an2 (2009), Abstract;


一般参考文献

1.

DNA measurement and cell cycle analysis by flow cytometry: R. Nunez; Curr. Issues Mol. Biol. 3, 67 (2001), Abstract;

2.

Methods in Cell Biology, Flow Cytometry: Z. Darzynkiewicz, H.A. Crissman and J.P. Robinson (editors and co-authors); Vol. I and II, (1994), Book,

产品编号 产品名称 产品规格 产品等级
ENZ-51014-100 Nuclear-ID® Green cell cycle kit for flow cytometry 
细胞周期检测试剂盒(绿色荧光)(流式)
1 Kit
ENZ-51008-100 Nuclear-ID® Red cell cycle kit (GFP-Certified®) for flow cytometry 
细胞核检测试剂盒(红色荧光)(GFP细胞)(荧光显微镜)
1 Kit

BD原装进口凋亡检测试剂盒(PE,7-ADD,FITC标记)559763 556547

详细介绍

BD原装进口凋亡检测试剂盒(PE,7-ADD,FITC标记)559763 556547

原装进口现货促销中

Technical Data Sheet

PE Annexin V Apoptosis Detection Kit I

Product Information

Material Number: 559763

Component: 51-66121E

Description: 10X Annexin V Binding Buffer

Size: 50 ml (1 ea)

Storage Buffer: Aqueous buffered solution containing no preservative.

Component: 51-68981E

Description: 7-AAD

Size: 2.0 ml (1 ea)

Vol. per Test: 5 μl

Storage Buffer: Aqueous buffered solution containing fetal bovine serum and ≤0.09% sodium

azide.

Component: 51-65875X

Description: PE Annexin V

Size: 0.5 ml (1 ea)

Vol. per Test: 5 μl

Storage Buffer: Aqueous buffered solution containing BSA and ≤0.09% sodium azide.

Description

Apoptosis is a normal physiologic process which occurs during embryonic development as well as in maintenence of tissue homeostasis. The

apoptotic program is characterized by certain morphologic features, including loss of plasma membrane asymmetry and attachment,

condensation of the cytoplasm and nucleus, and internucleosomal cleavage of DNA. Loss of plasma membrane is one of the earliest features.

In apoptotic cells, the membrane phospholipid phosphatidylserine (PS) is translocated from the inner to the outer leaflet of the plasma

membrane, thereby exposing PS to the external cellular environment. Annexin V is a 35-36 kDa Ca2+ dependent phospholipid-binding

protein that has a high affinity for PS, and binds to cells with exposed PS. Annexin V may be conjugated to fluorochromes including

Phycoerythrin (PE). This format retains its high affinity for PS and thus serves as a sensitive probe for flow cytometric analysis of cells that are

undergoing apoptosis. Since externalization of PS occurs in the earlier stages of apoptosis, PE Annexin V staining can identify apoptosis at an

earlier stage than assays based on nuclear changes such as DNA fragmentation.

PE Annexin V staining precedes the loss of membrane integrity which accompanies the latest stages of cell death resulting from either

apoptotic or necrotic processes. Therefore, staining with PE Annexin V is typically used in conjunction with a vital dye such as

7-Amino-Actinomycin (7-AAD) to allow the investigator to identify early apoptotic cells (7-AAD negative, PE Annexin V positive). Viable

cells with intact membranes exclude 7-AAD, wheras the membranes of dead and damaged cells are permeable to 7-AAD. For example, cells

that are considered viable are PE Annexin V and 7-AAD negative; cells that are in early apoptosis are PE Annexin V positive and 7-AAD

negative; and cells that are in late apoptosis or already dead are are both PE Annexin V and 7-AAD positive. This assay does not distinguish

between cells that have undergone apoptotic death versus those that have died as a result of a necrotic pathway because in either case, the dead

cells will stain with both PE Annexin V and 7-AAD. However, when apoptosis is measured over time, cells can be often tracked from PE

Annexin V and 7-AAD negative (viable, or no measurable apoptosis), to PE Annexin V positive and 7-AAD negative (early apoptosis,

membrane integrity is present) and finally to PE Annexin V and 7-AAD positive (end stage apoptosis and death). The movement of cells

through these three stages suggests apoptosis. In contrast, a single observation indicating that cells are both PE Annexin V and 7-AAD

positive, in of itself, reveals less information about the process by which the cells underwent their demise.

559763 Rev. 8 Page 1 of 3

Flow Cytometric Analysis of PE Annexin V staining. Jurkat cells

(Human T-cell leukemia; ATCC TIB-152) were left untreated (top

panels) or treated for 4 hours with 4 μM Camptothecin (bottom

panels). Cells were incubated with PE Annexin V in a buffer

containing 7-Amino-Actinomycin (7-AAD) and analyzed by flow

cytometry. Untreated cells were primarily PE Annexin V and 7-AAD

negative, indicating that they were viable and not undergoing

apoptosis. After a 4 hour treatment (bottom panels), there were

primarily two populations of cells: Cells that were viable and not

undergoing apoptosis (PE Annexin V and 7-AAD negative); cells

undergoing apoptosis (PE Annexin V positive and 7-AAD negative).

A minor population of cells were observed to be PE Annexin V and

7-AAD positive, indicating that they were in end stage apoptosis or

already dead.

Preparation and Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.

Application Notes

Application

Flow cytometry Routinely Tested

Recommended Assay Procedure:

PE Annexin V is a sensitive probe for identifying apoptotic cells, binding to negatively charged phospholipid surfaces (Kd of ~5 x 10^-2) with a

higher affinity for phosphatidylserine (PS) than most other phospholipids. PE Annexin V binding is calcium dependent and defined calcium and

salt concentrations are required for optimal staining as described in the PE Annexin V Staining Protocol. Investigators should note that PE

Annexin V flow cytometric analysis on adherent cell types (e.g HeLa, NIH 3T3, etc.) is not routinely tested as specific membrane damage

may occur during cell detachment or harvesting. Methods for utilizing Annexin V for flow cytometry on adherent cell types, however,

have been previously reported (Casiola-Rosen et al. and van Engelend et al.).

INDUCTION OF APOPTOSIS BY CAMPTOTHECIN

The following protocol is provided as an illustration on how PE Annexin V may be used on a cell line (Jurkat).

BD原装进口凋亡检测试剂盒(PE,7-ADD,FITC标记)559763 556547

Materials

1. Prepare Camptothecin stock solution (Sigma-Aldrich Cat. No. C-9911): 1 mM in DMSO.

2. Jurkat T cells (ATCC TIB-152).

Procedure

1. Add Camptothecin (final conc. 4-6 μM) to 1 x 10^6 Jurkat cells.

2. Incubate the cells for 4-6 hr at 37°C.

3. Proceed with the PE Annexin V Staining Protocol to measure apoptosis.

PE ANNEXIN V STAINING PROTOCOL

PE Annexin V is used to quantitatively determine the percentage of cells within a population that are actively undergoing apoptosis. It relies on

the property of cells to lose membrane asymmetry in the early phases of apoptosis. In apoptotic cells, the membrane phospholipid

phosphatidylserine (PS) is translocated from the inner leaflet of the plasma membrane to the outer leaflet, thereby exposing PS to the external

environment. Annexin V is a calcium-dependent phospholipid-binding protein that has a high affinity for PS, and is useful for identifying

apoptotic cells with exposed PS. 7-Amino-Actinomycin (7-AAD) is a standard flow cytometric viability probe and is used to distinguish viable

from nonviable cells. Viable cells with intact membranes exclude 7-AAD, whereas the membranes of dead and damaged cells are permeable to

7-AAD. Cells that stain positive for PE Annexin V and negative for 7-AAD are undergoing apoptosis. Cells that stain positive for both PE

Annexin V and 7-AAD are either in the end stage of apoptosis, are undergoing necrosis, or are already dead. Cells that stain negative for both PE

Annexin V and 7-AAD are alive and not undergoing measurable apoptosis.

559763 Rev. 8 Page 2 of 3

Reagents

1. PE Annexin V (component no. 51-65875X): Use 5 μl per test.

2. 7-Amino-Actinomycin (7-AAD) (component no. 51-68981E) is a convenient, ready-to-use nucleic acid dye. Use 5 μl per test.

3. 10X Annexin V Binding Buffer (component no. 51-66121E): 0.1 M Hepes/NaOH (pH 7.4), 1.4 M NaCl, 25 mM CaCl2. For a 1X working

solution, dilute 1 part of the 10X Annexin V Binding Buffer to 9 parts of distilled water.

Staining

1. Wash cells twice with cold PBS and then resuspend cells in 1X Binding Buffer at a concentration of 1 x 10^6 cells/ml.

2. Transfer 100 μl of the solution (1 x 10^5 cells) to a 5 ml culture tube.

3. Add 5 μl of PE Annexin V and 5 μl 7-AAD.

4. Gently vortex the cells and incubate for 15 min at RT (25°C) in the dark.

5. Add 400 μl of 1X Binding Buffer to each tube. Analyze by flow cytometry within 1 hr.

SUGGESTED CONTROLS FOR SETTING UP FLOW CYTOMETRY

The following controls are used to set up compensation and quadrants:

1. Unstained cells.

2. Cells stained with PE Annexin V (no 7-AAD).

3. Cells stained with 7-AAD (no PE Annexin V).

Other Staining Controls:

A cell line that can be easily induced to undergo apoptosis should be used to obtain positive control staining with PE Annexin V and/or PE

Annexin V and 7-AAD. It is important to note that the basal level of apoptosis and necrosis varies considerably within a population. Thus, even in

the absence of induced apoptosis, most cell populations will contain a minor percentage of cells that are positive for apoptosis (PE Annexin V

positive, 7-AAD negative or PE Annexin V positive, 7-AAD positive).

The untreated population is used to define the basal level of apoptotic and dead cells. The percentage of cells that have been induced to undergo

apoptosis is then determined by subtracting the percentage of apoptotic cells in the untreated population from percentage of apoptotic cells in the

treated population. Since cell death is the eventual outcome of cells undergoing apoptosis, cells in the late stages of apoptosis will have a damaged

membrane and stain positive for 7-AAD as well as for PE Annexin V. Thus the assay does not distinguish between cells that have already

undergone an apoptotic cell death and those that have died as a result of necrotic pathway, because in either case the dead cells will stain with

both PE Annexin V and 7-AAD.

Product Notices

This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-μl experimental

sample (a test).

1.

2. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before

discarding to avoid accumulation of potentially explosive deposits in plumbing.

3.

4. Please refer to www.bdbiosciences.com/pharmingen/protocols for technical protocols.

References

Andree HA, Reuingsperger CP, Hauptmann R, Hemker HC, Hermens WT, Willems GM. Binding of vascular anticoagulant alpha (VAC alpha) to planar

phospholipid bilayers. J Biol Chem. 1990; 265(9):4923-4928. (Biology)

Casciola-Rosen L, Rosen A, Petri M, Schlissel M. Surface blebs on apoptotic cells are sites of enhanced procoagulant activity: implications for coagulation events

and antigenic spread in systemic lupus erythematosus. Proc Natl Acad Sci U S A. 1996; 93(4):1624-1629. (Biology)

Homburg CH, de Haas M, von dem Borne AE, Verhoeven AJ, Reuingsperger CP, Roos D. Human neutrophils lose their surface Fc gamma RIII and acquire

Annexin V binding sites during apoptosis in vitro. Blood. 1995; 85(2):532-540. (Biology)

Koopman G, Reuingsperger CP, Kuijten GA, Keehnen RM, Pals ST, van Oers MH. Annexin V for flow cytometric detection of phosphatidylserine expression on

B cells undergoing apoptosis. Blood. 1994; 84(5):1415-1420. (Biology)

Martin SJ, Reuingsperger CP, McGahon AJ, et al. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of

the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl. J Exp Med. 1995; 182(5):1545-1556. (Biology)

Raynal P, Pollard HB. Annexins: the problem of assessing the biological role for a gene family of multifunctional calcium- and phospholipid-binding proteins.

Biochim Biophys Acta. 1994; 1197(1):63-93. (Biology)

van Engeland M, Ramaekers FC, Schutte B, Reuingsperger CP. A novel assay to measure loss of plasma membrane asymmetry during apoptosis of adherent

cells in culture. Cytometry. 1996; 24(2):131-139. (Biology)

Vermes I, Haanen C, Steffens-Nakken H, Reuingsperger C. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early

apoptotic cells using fluorescein labelled Annexin V. J Immunol Methods. 1995; 184(1):39-51. (Biology)

 

详细产品信息可和选购!