TUNEL Assay试剂盒- BrdU-Red (ab66110)
Key features and details
- Assay type: Quantitative
- Detection method: Fluorescent
- Platform: Flow cytometer, Fluorescence microscope
- Assay time: 3 hr
- Sample type: Adherent cells, Suspension cells, Tissue
概述
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产品名称
TUNEL Assay试剂盒- BrdU-Red
参阅全部 DNA fragmentation 试剂盒 -
检测方法
Fluorescent -
样品类型
Tissue, Adherent cells, Suspension cells -
检测类型
Quantitative -
检测时间
3h 00m -
种属反应性
与反应: Mammals, Other species -
产品概述
TUNEL Assay Kit - BrdU-Red ab66110 uses a convenient and sensitive method to detect DNA fragmentation by flow cytometry and fluorescence microscopy in live cells.
The TUNEL assay is used to detect DNA fragmentation, such as in apoptosis. It uses terminal deoxynucleotidyl transferase (TdT) to catalyze the incorporation of deoxynucleotides at the free 3'-hydroxyl ends of fragmented DNA. The deoxynucleotides are then labeled in a variety of ways for detection of the degree of DNA fragmentation.
This TUNEL assay protocol is based on Br-dUTP (bromolated deoxyuridine triphosphate nucleotide), which can be more readily incorporated into DNA strand breaks by the TdT enzyme than other dUTP labels such as FITC, biotin or dioxigenin. The greater incorporation rate produces a brighter signal when the Br-dUTP sites are detected with an anti-BrdU monoclonal antibody directly labeled with a red fluorochrome.
The BrdU-Red signal can be analyzed at Ex/Em 488/576 nm, with an optional 7-AAD counterstain at Ex/Em 488/655nm.
This TUNEL assay kit includes both negative and positive control cells. It is designed to be suitable for studying DNA fragmentation in GFP-transfected cells.
Tunel assay protocol summary:
- fix cells / tissues with formaldehyde, or deparaffinize and rehydrate if paraffin sections, and wash
- incubate cells in 70% ethanol for 30 min at 4ºC, or if tissues incubate with proteinase K solution for 5 min at room temp and refix with formaldehyde
- wash
- incubate in DNA labeling solution for 60 min at 37ºC
- wash
- incubate in antibody solution for 30 min at room temp
- add 7-AAD / RNase A solution and incubate for 30 min at room temp
- analyze with flow cytometry or fluorescent microscopy -
说明
This product is manufactured by BioVision, an Abcam company and was previously called K404 ApoBrdU Red DNA Fragmentation Kit. K404-60 is the same size as the 60 test size of ab66110.
This kit is BrdU-Red labeled (Ex/Em = 488/576 nm). It was previously called TUNEL Assay Kit - In situ BrdU-Red DNA Fragmentation.
To use FITC (Ex/Em = 495/519 nm) as a label, we recommend TUNEL Assay Kit - FITC (ab66108).
For chromogenic TUNEL staining, we recommend TUNEL Assay Kit - HRP-DAB ab206386.
Find out more about the TUNEL method in the TUNEL staining / TUNEL assay guide.
Abcam has not and does not intend to apply for the REACH Authorisation of customers’ uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses. -
平台
Flow cytometer, Fluorescence microscope
性能
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存放说明
Please refer to protocols. -
组件 60 tests 60 tests 7-AAD/RNase Staining Buffer 1 x 30ml 1 x 30ml Anti-BrdU-Red Antibody 1 x 300µl 1 x 300µl Br-dUTP 1 x 480µl 1 x 480µl Negative Control Cells 1 x 5ml 1 x 5ml Positive Control Cells 1 x 5ml 1 x 5ml Reaction Buffer 1 x 600µl 1 x 600µl Rinse Buffer 1 x 120ml 1 x 120ml TdT Enzymes 1 x 45µl 1 x 45µl Wash Buffer 1 x 120ml 1 x 120ml -
研究领域
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相关性
Internucleosomal DNA fragmentation is a hallmark of apoptosis in mammalian cells.
相关产品
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Assay kits
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Related Products
图片
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Detection of DNA fragmention (TUNEL staining) using the negative and positive control cells (HL-60 untreated and treated with camptothecin). Cells were stained following the assay protocol. The fluorescence signal was detected and analyzed using BD FACScan System (Becton Dickinson).
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TUNEL staining in whole mount Hydractinia echinata using In situ BrdU-Red DNA Fragmentation (TUNEL) Assay Kit (ab66110).
Animals were fixed in 4% PFA in PBS for 1 hour and processed as per the protocol without proteinaseK treatment. In place of proteinaseK animals were permeabilised in 3% Triton in PBS for 15 minutes. Animals were counter-stained with DAPI.
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Immunohistochemical analysis of paraffin embedded 5 micron thick testis tissues of 8 week old Stag3+/− and Stag3−/− (Stromal antigen) mice . Apoptotic cells were detected using In situ BrdU-Red DNA Fragmentation (TUNEL) Assay Kit (ab66110). DAPI was used as a counterstain.
数据表及文件
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SDS download
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Datasheet download
文献 (123)
ab66110 被引用在 123 文献中.
- Notorgiacomo G et al. A bioreactor for studying negative pressure wound therapy on skin grafts. Int Wound J 19:633-642 (2022). PubMed: 34235863
- Sandovici I et al. The imprinted Igf2-Igf2r axis is critical for matching placental microvasculature expansion to fetal growth. Dev Cell 57:63-79.e8 (2022). PubMed: 34963058
- Bi Y et al. ERp44 is required for endocardial cushion development by regulating VEGFA secretion in myocardium. Cell Prolif 55:e13179 (2022). PubMed: 35088919
- Kim H et al. Ultraefficient extracellular vesicle-guided direct reprogramming of fibroblasts into functional cardiomyocytes. Sci Adv 8:eabj6621 (2022). PubMed: 35213232
- Sakuma C et al. Histological and Immunohistochemical Studies to Determine the Mechanism of Cleft Palate Induction after Palatal Fusion in Mice Exposed to TCDD. Int J Mol Sci 23:N/A (2022). PubMed: 35216185