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- 英文名:
APO-BRDU Kit
- 库存:
1
- 供应商:
研卉生物
- 规格:
60 Tests
| Tunel凋亡晚期 |
Description
| / | 产品编号 | 产品名称 | 规格 |
| 凋亡早期 | 556547 | BD Pharmingen™FITC Annexin V Apoptosis Detection Kit | 100T |
| 凋亡早期 | 559763 | BD Pharmingen™PE Annexin V Apoptosis Detection Kit | 100T |
| 线粒体膜电位 | 551302 | MitoScreen JC-1 Kit | 100T |
| Caspase-3 | 550914 | PE Active Caspase-3 Apoptosis Kit |
Kit |
| Tunel凋亡晚期 | 556405 | APO-BRDU™ Kit | 60T |
One of the later steps in apoptosis is DNA fragmentation, a process which results from the activation of endonucleases during the apoptotic program. These nucleases degrade the higher order chromatin structure into fragments of ~300 kb and subsequently into smaller DNA pieces of about 50 bp length. A method which is often used to detect fragmented DNA utilizes a reaction catalyzed by exogenous TdT, often referred to as "end-labeling" or "TUNEL" (terminal deoxynucleotidyltransferase dUTP nick end labeling). In the APO-BRDU™ assay, TdT catalyzes a template-independent addition of bromolated deoxyuridine triphosphates (Br-dUTP) to the 3'-hydroxyl (OH) termini of double- and single-stranded DNA. After incorporation, these sites are identified by flow cytometric means by staining the cells with a FITC-labeled anti-BrdU mAb. The APO-DIRECT™ assay (Cat. No. 51-6536KK) is a single-step method for labeling DNA breaks with FITC-dUTP, followed by flow cytometric analysis.
The APO-BRDU™ Kit is a two color staining method for labeling DNA breaks and total cellular DNA to detect apoptotic cells by flow cytometry. Sufficient reagents are provided to process 60 cell suspensions. The kit includes 5 ml of positive and 5 ml of negative control cell suspensions, approximately 1 x 10^6 cells per ml in 70% (v/v) ethanol. The control cells are derived from a human lymphoma cell line and have been fixed as described in the Fixation Protocol.
The APO-BRDU™ Kit consists of two parts (part A and B).
Part A (Comp. No. 51-6576AK) consists of:
One 0.30 ml bottle of FITC-Labeled Anti-BrdU mAb [Isotype: mouse; 1 µg/test (contains 0.05% sodium azide)] (Comp. No. 51-6584AZ]
One 30 ml bottle of PI/RNase Staining Buffer (5 µg/ml, 200 µg/ml RNase) [Comp. No. 51-6585AZ]
One 0.6 ml vial of Reaction Buffer (containing cacodylic acid (dimethylarsenic)) [Comp. No. 51-6580AZ ]
One 126 ml bottle of Rinsing Buffer (containing 0.05% sodium azide) [Comp. No. 51-6583AZ]
One 120 ml botle of Wash Buffer (containing 0.05% sodium azide) [Comp. No. 51-6579AZ].
Part B (Comp. No. 51-6576BK) consists of:
One 0.48 ml bottle of Br-dUTP (54.7 µg/ml) [Comp. No. 51-6582EZ]
One 5 ml bottle of Negative Control Cells [contains 70% (v/v) ethanol] [Comp. No. 51-6578LZ]
One 5 ml bottle of Positive Control Cells [contains 70% (v/v) ethanol] [Comp. No. 51-6577LZ}
One 0.045 ml bottle of TdT Enzyme [200 µg/ml (S.A.= 100,000 U/mg) in 50% (v/v) glycerol solution; will not freeze at -20°C] [Comp. No. 51-6581EZ]
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文献和实验0-G1期峰的一个峰,死亡的细胞峰离G0-G1期峰较远,但是这种典型的结果似乎很难获得。有其它的替代方法,完全可以不用这种方法。晚期凋亡的细胞由于DNA的断裂,因而可以出现DNA ladder,从而也就有了经典的检测方法TUNEl。流式也能进行Tunel检测,其检测原理与经典Tunel原理基本一致。以BD公司的为例,其利用TdT能将荧光素标记的dUTP标记到断裂的DNA末端,从而使凋亡的细胞具有荧光。但是由于在细胞内标记,细胞需要进行固定处理,操作类似免疫组织化学法,容易造成假阳性。建议采用原装大厂
细胞凋亡晚期中,核酸内切酶(某些Caspase的底物)在核小体之间剪切核DNA,产生大量长度在180-200 bp 的DNA片段。对于这一现象的检测通常有以下几种方法: 1 TUNEL(Terminal deoxynucleotidyl transferase-mediated dUTP nick-end-labeling) 通过DNA末端转移酶将带标记的 dNTP (多为dUTP)间接(通过地高辛)或直接接到DNA片段的3’-OH端,再通
示例: Jurkat细胞用1μM喜树碱(Camptothecin) (左)或未加药 (右)处理4h,FITC-Annexin V/PI荧光双染细胞凋亡检测试剂盒染色后,流式细胞仪荧光检测。 Annexin V-FITC单阳性细胞为早期凋亡细胞,Annexin V-FITC和PI染色双阳性的细胞为坏死细胞或者晚期凋亡。PI单染色阳性位裸核细胞。 实测数据可能会因细胞类型、细胞凋亡情况,检测仪器等的不同而存在差异,图中数据仅供参考。 流式检测细胞凋亡的数据分析方法: 1) 选中所有颗粒,将FSC
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