OxiSelect™ DNA Double Strand Break (DSB) Staining Kit, Trial Size
Specifications | |
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Research Area: | Oxidative Stress |
Assay Category: | DNA/RNA Damage and Repair Assays |
Detection Method: | Immunofluorescence |
Product Description
- Detects phosphorylation of histone H2A.X
- See immunofluorescence in about 3 hours
- DNA double-strand break inducer included
DNA double-strand breaks (DSBs) are probably the most dangerous of the many different types of DNA damage that occur within the cell. DSBs are generated by exogenous agents such as ionizing radiation (IR) or by endogenously generated reactive oxygen species and occur as intermediates during meiotic and V(D)J recombination. A very early step in the cellular response to DSBs is the
phosphorylation of a histone H2A variant, H2AX, at the sites of DNA damage. H2AX is rapidly phosphorylated (within seconds) at serine 139 when DSBs are introduced into mammalian cells resulting in discrete gamma-H2AX (phosphorylated H2AX) foci at the DNA damage sites. H2AX phosphorylation also appears to be a general cellular response to processes involving DSB intermediates including V(D)J recombination in lymphoid cells and meiotic recombination in mice. Phosphorylation of H2A at serine 139 causes chromatin decondensation and appears to play a critical role in the recruitment of repair or damage-signaling factors to the sites of DNA damage.
Cell Biolabs’ OxiSelect DNA DSB Staining Kit is based on the phosphorylation of the histone H2A.X at serine 139 in response to DNA damaging agents which cause double strand breaks in cells that are cultured in microtiter plates. The kit provides sufficient reagents for up to 100 stainings in 96-well plate.
Product Citations
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- Shirasugi, M. et al. (2016) Normal human gingival fibroblasts undergo cytostasis and apoptosis after long-term exposure to butyric acid. Biochem.
- Wu, S. T. et al. (2016) Cellular effects induced by 17-β-estradiol to reduce the survival of renal cell carcinoma cells. J Biomed Sci
- Dokic, I. et al. (2014) High resistance to X-rays and therapeutic carbon ions in glioblastoma cells bearing dysfunctional ATM associates with intrinsic chromosomal instability. Int J Radiat Biol.
- Edwards, A.K. et al. (2014) A peptide inhibitor of synuclein-g reduces neovascularization of human endometriotic lesions. Mol Hum Reprod.
- Catalog Number
STA-321-T-CB - Supplier
Cell Biolabs - Size
- Shipping
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