| 產(chǎn)品編號(hào) | BA00103 |
| 英文名稱 | Annexin V-AF647 Apoptosis Detection Kit |
| 中文名稱 | Annexin V-AF647細(xì)胞凋亡檢測(cè)試劑盒 |
| 別 名 | Annexin V-AF647/PI Apoptosis Detection Kit; Annexin V-AF647 Apoptosis Detection Kit; Annexin V-AbBy Fluor? 647/PI Kit; Annexin V-AbBy Fluor? 647/PI Kit; Annexin V-AF647/PI Kit; Annexin V-AF647/PI雙染細(xì)胞凋亡檢測(cè)試劑盒; Annexin V-AF647細(xì)胞凋亡檢測(cè)試劑盒; AF647 Annexin V/PI細(xì)胞凋亡檢測(cè)試劑盒; Annexin V-AF647/PI雙染細(xì)胞凋亡檢測(cè)試劑盒; ANNEXIN V- AF647凋亡檢測(cè)試劑盒; Annexin V-AF647/PI細(xì)胞凋亡檢測(cè)試劑盒; 細(xì)胞凋亡檢測(cè)試劑盒; 細(xì)胞凋亡試劑盒; |
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Specific References (2) | BA00103 has been referenced in 2 publications.
[IF=10.164] Wang D et al. Loss of 4.1N in epithelial ovarian cancer results in EMT and matrix-detached cell death resistance.. Protein Cell. 2020 May 25. FCM ; Human.
[IF=5.714] Xiangming Liu. et al. Taxifolin ameliorates cigarette smoke-induced chronic obstructive pulmonary disease via inhibiting inflammation and apoptosis. INT IMMUNOPHARMACOL. 2023 Feb;115:109577
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| 克 隆 號(hào) | |
| CAS | |
| 理論分子量 | kDa |
| 檢測(cè)分子量 | |
| 保存條件 | Store at 4℃. |
| 注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 產(chǎn)品介紹 |
磷脂酰絲氨酸（PS）是一種帶負(fù)電荷的磷脂，正常細(xì)胞中，PS只分布在細(xì)胞膜脂質(zhì)雙層的內(nèi)側(cè)，而在細(xì)胞凋亡早期，細(xì)胞膜 PS由脂膜內(nèi)側(cè)翻向細(xì)胞膜外側(cè)，使PS暴露在細(xì)胞膜外表面。Annexin V是一種分子量為35~36kD 的Ca2+依賴性磷脂結(jié)合蛋白，與磷脂酰絲氨酸有高度親和力，故可通過(guò)細(xì)胞外側(cè)暴露的磷脂酰絲氨酸與凋亡早期細(xì)胞的胞膜結(jié)合。因此Annexin V被公認(rèn)為檢測(cè)細(xì)胞早期凋亡的靈敏指標(biāo)之一。 將Annexin V進(jìn)行Alexa Fluor 647標(biāo)記，以標(biāo)記了的Annexin V作為探針，利用熒光顯微鏡或流式細(xì)胞儀可檢測(cè)細(xì)胞凋亡的發(fā)生。碘化丙啶（Propidium Iodide, PI）是一種核酸染料，它不能透過(guò)正常細(xì)胞或早期凋亡細(xì)胞的完整的細(xì)胞膜，但對(duì)凋亡中晚期的細(xì)胞和壞死細(xì)胞，PI能夠透過(guò)細(xì)胞膜而使細(xì)胞核染紅。因此采用Annexin V與PI雙染的方法，就可以將處于不同凋亡時(shí)期的細(xì)胞區(qū)分開來(lái)。 |
| 產(chǎn)品圖片 |
Jurkat cells (T-cell leukemia,human) treated with 10 μM of camptothecin for 4 hours(panel right) or untreated control(panel left).
1. Wash cells twice with cold PBS and then resuspend cells in 1×Binding Buffer at a concentration of 1×106 cells/ml.
2. Transfer 100 μl of the solution (1×105cells) to a 5 ml culture tube.
3. Add 5 μl of Annexin V-AF647.
4. Add 5 μl PI.
5. Gently vortex the cells and incubate for 15 min at RT (25°C) in the dark.
6. Add 400 μl of 1×Binding Buffer to each tube.Analyze by flow cytometry within 1 hr.
外觀及包裝
外觀及包裝
外觀及包裝
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