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ApoDIRECT DNA Fragmentation Assay Kit

ABIN411729 产品详细信息, 供应商: Log in to see
适用
DNA
应用范围
Detection (D), Fluorescence Microscopy (FM), Flow Cytometry (FACS)
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原理 ApoDIRECT In Situ DNA Fragmentation Assay Kit provides complete components including positive and negative control cells for conveniently detecting DNA fragmentation by fluorescence microscopy or flow cytometry. The TUNEL-based detection kit utilizes terminal deoxynucleotidyl transferase (TdT) to catalyze incorporation of fluorescein-12-dUTP at the free 3'-hydroxyl ends of the fragmented DNA. The fluorescein-labeled DNA can then be observed by fluorescence microscopy or analyzed by flow cytometry.
品牌 ApoDIRECT™
样品类型 Adherent Cell Culture, Cell Culture Cells, Biological Fluids
检测方法 Fluorometric
特异性 ApoDIRECT In Situ DNA Fragmentation Assay Kit provides complete components including positive and negative control cells for conveniently detecting DNA fragmentation by fluorescence microscopy or flow cytometry. The TUNEL-based detection kit utilizes terminal deoxynucleotidyl transferase (TdT) to catalyze incorporation of fluorescein-12-dUTP at the free 3'-hydroxyl ends of the fragmented DNA. The fluorescein-labeled DNA can then be observed by fluorescence microscopy or analyzed by flow cytometry.
产品特性 ApoDIRECT In Situ DNA Fragmentation Assay Kit: Convenient & Reliable TUNEL-based Detection Kit to Detect DNA Fragmentation by Fluorescence Microscopy or Flow Cytometry. Includes both Positive and Negative Control Cells.
组件
  • Positive Control Cells
  • Negative Control Cells
  • Wash Buffer
  • Reaction Buffer
  • TdT Enzymes
  • FITC-dUTP
  • Rinse Buffer
  • PI/RNase Staining Buffer
背景 Internucleosomal DNA fragmentation is a hallmark of apoptosis in mammalian cells.
应用备注 Detection method: Flow cytometry (Ex/Em = 488/520 nm for FITC, and 488/623 nm for PI) and Fluorescence microscopy (FITC and rhodamine filters)
Applications: The TUNEL-based assay kit provides complete components including positive and negative control cells for convenient detection of DNA fragmentation in cultured cells and tissue sections.
说明

Flow cytometry (Ex/Em = 488/520 nm for FITC, and 488/623 nm for PI) and fluorescence microscopy (FITC and rhodamine filters)
Simple procedure, takes ~ 1 hour
Fast and convenient
The assay is sensitive and stable
The assay offers an one-step labeling of apoptotic cells.

实验流程 A. Cell fixation
1. Induce apoptosis in cells by desired method. Concurrently incubate a control culture without induction.
2. Pellet 1-5 x 10^6 cells at 300 x g and resuspend in 0.5 mL of PBS.
3. fix the cells by adding 5 mL of 1 % (w/v) paraformaldehyde in PBS and place on ice for 15 minutes.
4. Centrifuge the cells for 5 min at 300 x g and discard the supernatant.
5. Wash the cells in 5 mL of PBS and pellet the cells by centrifugation. Repeat one time the wash and centrifugation step.
6. Resuspend the cells in 0.5 mL of PBS.
7. Add the cells to 5 mL of ice-cold 70 % (v/v) ethanol. Let cells stand for a minimum of 30 min in ice or in the freezer.
8. Store the cells in 70 % (v/v) ethanol at -20 °C until use. Cells can be stored at - 20 °C for several days before use. B. Apo-DIRECT The procedures can be used for both control cells and your testing cells.
1. Resuspend the fixed cells by swirling the vials. Remove 1 mL aliquots of the cell suspension (approx. 1 x 10^6 cells per ml) and place in 12 x 75 mm tubes. Centrifuge (300 x g) cells for 5 min and carefully remove the ethanol by aspiration.
2. Resuspend each tube of cells with 1 mL of Wash Buffer (blue cap). Centrifuge as before and remove supernatant carefully by aspiration.
3. Repeat one time the washing step (step 2).
4. Resuspend each tube of the cells in 50 µL of the Staining Solution prepared as below:
5. Incubate the cells in the Staining Solution for 60 min at 37 °C. Shake cells every 15 min to resuspend.
6. Add 1 mL of Rinse Buffer (red cap) to each tube and centrifuge (300 x g) for 5 min. Remove supernatant by aspiration.
7. Repeat the rinsing step (step 6).
8. Resuspend the cell pellet in 0.5 mL of Propidium Iodide/RNase A Solution (amber bottle).
9. Incubate the cells in the dark for 30 min at room temperature.
10. Analyze the cells by fluorescence microscopy (apoptotic cells show green staining over an orange-red PI counter-staining) or flow cytometry. Cells should be analyzed within 3 hours of staining.
限制 仅限研究用
储存条件 -20 °C
有效期 12 months
有引用在: Apelbaum, Yarden, Warszawski, Harari, Schreiber: "Type I interferons induce apoptosis by balancing cFLIP and caspase-8 independent of death ligands." in: Molecular and cellular biology, Vol. 33, Issue 4, pp. 800-14, 2013 (PubMed).

Bahl, Hüebner, Davis, Welsh: "Analysis of apoptosis of memory T cells and dendritic cells during the early stages of viral infection or exposure to toll-like receptor agonists." in: Journal of virology, Vol. 84, Issue 10, pp. 4866-77, 2010 (PubMed).

Goplen, Bougnaud, Rajcevic, Bøe, Skaftnesmo, Voges, Enger, Wang, Tysnes, Laerum, Niclou, Bjerkvig: "αB-crystallin is elevated in highly infiltrative apoptosis-resistant glioblastoma cells." in: The American journal of pathology, Vol. 177, Issue 4, pp. 1618-28, 2010 (PubMed).

Vogt, Geddes, Bross, Blackstone: "Physiological characterization of stolon regression in a colonial hydroid." in: The Journal of experimental biology, Vol. 211, Issue Pt 5, pp. 731-40, 2008 (PubMed).