eBioscience™ Annexin V 细胞凋亡检测试剂盒
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eBioscience™ Annexin V 细胞凋亡检测试剂盒

这些试剂盒利用活力染料偶联膜联蛋白 V 来标记细胞外膜上的磷脂酰丝氨酸(PS;细胞凋亡早期标记物)。
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货号数量激发/发射偶联物
BMS500FI-100100 次测试488、535/520、617FITC、碘化丙啶
88-8005-74200 次测试488、535/520、617FITC、碘化丙啶
88-8006-7250 次测试405、546/450、647eFluor 450、7-AAD
88-8006-74200 次测试405、546/450、647eFluor 450、7-AAD
88-8007-74200 次测试650、535/660、617APC、碘化丙啶
88-8008-7250 次测试PCP-eFluor 710
88-8008-74200 次反应PCP-eFluor 710
BMS500FI-2020 次测试488、535/520、617FITC、碘化丙啶
BMS500FI-300300 次测试488、535/520、617FITC、碘化丙啶
88-8102-7250 次测试PE、7-AAD
88-8102-74200 次测试PE、7-AAD
88-8103-7250 次测试PE/Cy7
88-8103-74200 次测试PE/Cy7
BMS500BT-100
又称 BMS500BT/100
100 次测试NA、535/NA、617生物素、碘化丙啶
BMS500BT-20
又称 BMS500BT/20
20 次测试NA、535/NA、617生物素、碘化丙啶
BMS500BT-300
又称 BMS500BT/300
300 次测试NA、535/NA、617生物素、碘化丙啶
88-8005-7250 次测试488、535/520、617FITC、碘化丙啶
88-8007-7250 次测试650、535/660、617APC、碘化丙啶
货号 BMS500FI-100
价格(CNY)
2,096.00
飞享价
Ends: 31-Dec-2025
2,785.00
共减 689.00 (25%)
Each
添加至购物车
数量:
100 次测试
激发/发射:
488、535/520、617
偶联物:
FITC、碘化丙啶
价格(CNY)
2,096.00
飞享价
Ends: 31-Dec-2025
2,785.00
共减 689.00 (25%)
Each
添加至购物车
使用用于进行流式细胞分析的 eBioscience 和 Annexin V 细胞凋亡检测试剂盒,可轻松区分早期和晚期细胞凋亡。这些试剂盒利用活力染料偶联膜联蛋白 V 标记细胞外膜上的磷脂酰丝氨酸(PS;细胞凋亡早期标记物)。在晚期细胞凋亡中,随着细胞完整性的丧失,膜联蛋白 V 和活力染料横穿质膜并结合质膜内部的 PS。
膜联蛋白是一系列钙离子依赖型磷脂结合蛋白,可优先结合磷脂酰丝氨酸 (PS)。在正常生理条件下,PS主要位于质膜的内叶。细胞凋亡开始时,PS 会丢失其在磷脂双分子层上的不对称分布,并且可以转运至细胞外膜叶上,以标记细胞作为吞噬作用的靶标。在细胞膜外表面时,可通过荧光标记的膜联蛋白 V 在钙离子依赖模式下检测 PS。

在细胞凋亡早期,质膜可阻挡碘化丙啶 (PI)、7-AAD 等活力染料或者 eFluor 450 等可固定活力染料进入细胞。这些细胞会被膜联蛋白 V 染色,但不被活力染料染色,从而能够在早期细胞凋亡中区分出细胞。然而,在细胞凋亡晚期,细胞膜丧失完整性,因此膜联蛋白 V 也可接触细胞内的 PS。活力染料可用于从早期凋亡细胞(膜联蛋白 V 阳性,活力染料阴性)中分辨出这些晚期凋亡和坏死细胞(膜联蛋白 V、活力染料阳性)。

目前随 eBioscience 膜联蛋白 V 细胞凋亡检测试剂盒提供的活力染料包括 FITC、eFluor 450、别藻蓝蛋白 (APC)、藻红蛋白 (PE)、PE-cyanine7 和生物素。

仅供科研使用。不可用于诊断程序。
规格
描述eBioscience Annexin V-FITC Apoptosis Detection Kit
激发/发射488、535/520、617
适用于(设备)流式细胞仪
套装内容• 结合缓冲液 (4X),1 瓶 (50 mL)
• rh Annexin V-FITC,1 小瓶 (0.5 mL)
• 碘化丙啶 (20 µg/mL),1 小瓶 (1.8 mL)
产品类型细胞凋亡检测试剂盒
数量100 次测试
运输条件湿冰
偶联物FITC、碘化丙啶
Unit SizeEach
内容与储存
2°C 至 8°C。避免温度波动。

常见问题解答 (FAQ)

Is annexin V specific for any particular species?

Annexin V binding of phospholipids is not species-specific. In the presence of millimolar concentrations of Ca2+, Annexin V binds to several phospholipids, but exhibits the highest affinity for phosphatidylserine. This feature is useful for screening cells undergoing apoptosis. Phosphatidylserine is usually distributed on the inner leaflet of the lipid bilayer, but when cells start to undergo apoptosis, the phosphatidylserine moves to the outer leaflet. The translocation of phosphatidylserine to the outer leaflet makes it available for Annexin V staining. Normal, intact cells will not stain with Annexin V, while cells undergoing apoptosis will be.

Annexin V staining can be visualized by fluorescence microscopy or flow cytometry using conjugates such as Annexin V-FITC, or Annexin V-biotin in conjugation with a streptavidin-conjugated fluorophore. It is important to note that experiments with Annexin V require that the cells under study are live cells with intact membranes. It is not suitable for use with fixed cells as the membrane develops holes during the fixation process, making the phosphatidylserine on the inner face of the membrane accessible for Annexin V binding. For similar reasons, this product is also not suitable for use with tissue sections. Because necrotic cells also have numerous membrane breaches, these cells are also often stained with Annexin V. A quick way to differentiate apoptotic from necrotic cells is with a double staining regime using Annexin V-FITC (green fluorescence) and the DNA staining dye propidium iodide (red fluorescence). Propidium iodide requires membrane breaches in order to gain access to the cell nucleus.

Using the Annexin V-FITC/propidium iodide double staining regime, the following staining patterns are observed with apoptotic and necrotic cells:
1. Cells that are normal will not stain with either Annexin V-FITC or propidium iodide (indicating no phosphatidylserine on the surface and no holes in the membrane).
2. Cells that are starting to undergo apoptosis will stain with Annnexin V-FITC only (indicating phosphatidylserine on the surface but no holes in the membrane).
3. Cells that are in late apoptosis and necrotic cells will stain with both Annexin V-FITC and with propidium iodide (indicating that we cannot tell where the phosphatidylserine is located and that there are holes in the membrane).

Phosphatidylserine is an ubiquitous membrane component among mammalian species; therefore, we believe that Annexin V has utility in monitoring apoptosis with any mammalian-derived cell line. One report (O'Brien et al., 1997) has even indicated its utility in monitoring apoptosis with plant cells. Dive, C., C.D. Gregory, D.J. Phipps, D.L. Evans, A.E. Milner, and A.H. Wyllie (1992) Analysis and discrimination of necrosis and apoptosis (programmed cell death) by multiparameter flow cytometry. Biochem. Biophys. Acta 1133:275-285. Koopman, G., C.P.M. Reutlingsperger, G.A.M. Kuitjen, R.M.J. Keehnen, S.T. Pals, and M.H.J. van Oers (1994) Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis. Blood 84:1415-1420. O'Brien, I.E., C.P. Reutelingsperger, and K.M. Holdaway (1997) Annexin-V and TUNEL use in monitoring the progression of apoptosis in plants. Cytometry 29(1):28-33.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Can I use eFluor 450-conjugated antibodies with eBioscience Annexin V Apoptosis Detection kits?

Yes, eFluor 450-conjugated antibodies are compatible with eBioscience Annexin V Apoptosis Detection kits.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.