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Alexa Fluor® 488 anti-H2A.X Phospho (Ser139) A
产品名称：
Alexa Fluor® 488 anti-H2A.X Phospho (Ser139) A
产品类别：
抗体
产品编号：
613406
产品应用：
613406
[价格]
规格 价格 库存
100tests ￥ 4440 1

产品详情

Product Details

Verified Reactivity
Human, Mouse
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
Modified peptide
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA)
Preparation
The antibody was purified by affinity chromatography and conjugated with Alexa Fluor? 488 under optimal conditions.
Concentration
Lot-specific (to obtain lot-specific concentration, please enter the lot number in our Concentration and Expiration Lookup or Certificate of Analysis online tools.)
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

ICFC - Quality tested
Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent intracellular staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is 5 ?l per million cells.

* Alexa Fluor? 488 has a maximum emission of 519 nm when it is excited at 488 nm.


Alexa Fluor? and Pacific Blue? are trademarks of Life Technologies Corporation.

View full statement regarding label licenses
Excitation Laser
Blue Laser (488 nm)
Application Notes

Additional reported applications (for the relevant formats of this clone) include: immunohistochemistry on paraffin embedded sections2, immunofluorescence microscopy3-9, Western blotting 10-12, and flow cytometry1,13. Clone 2F3 cross-reacts with mouse4.

Intracellular staining protocol for Anti-H2A.X-Phosphorylated (Ser139) Antibody for Flow Cytometry

1. Prepare 70% absolute ethanol. Chill solution by storing at -20°C.
2. Prepare cells of interest.
3. Wash 1X with PBS, centrifuge at 350g for 5 min.
4. Discard the supernatant and vortex to loosen cell pellet.
5. Add pre-cooled 70% ethanol drop by drop, while vortexing.
6. Incubate at -20°C for 60 minutes.
7. Wash 3X with BioLegend Cell Staining Buffer and resuspend the cells at 0.5-1 X 107 cells/ml in the cell staining buffer.
8. Perform immunofluorescent staining for flow cytometry.

Application References

(PubMed link indicates BioLegend citation)
  1. Jha JC, et al. 2013. J. Virol. 87:5255. (FC) PubMed
  2. Akbay A, et al. 2008. Am J Pathol. 173:536. (IHC) PubMed
  3. Mochizuki K, et al.2008.J cell Sci.121:2148. (IF) PubMed
  4. Xiao R, et al. 2007. Mol Cell Biol.27:5393. (IF) PubMed
  5. Rossi DJ, et al. 2007. Nature. 447:725. (IF) PubMed
  6. Loidl J, et al. 2009. Mol Cell Biol. 20:2048. (IF) PubMed
  7. Beels L, et al. 2009. Circulation. 120:1903. (IF) PubMed
  8. Suzuki K, et al. 2010. Nucleic Acids Res. 38:e129. (IF) PubMed
  9. Lukaszewicz A. 2010. Chromasoma Apr 27. [Epub ahead of print] (IF) PubMed
  10. Yamada C, et al. 2010 J. Biol. Chem. 285:16693. (WB) PubMed
  11. Bu Y, et al. 2010, Biochem Biophys Res Commun. 397:157. (WB) PubMed
  12. Massignan T, et al. 2010. J. Biol Chem. 285:7752. (WB) PubMed
  13. Banath JP, et al. 2010. BMC Cancer 10:4 (FC)
  14. Zhang M., et al. 2011. Cancer Res. 23:7155. PubMed
  15. Kuefner MA, et al. 2012. Radiology 264:59. PubMed
  16. Yoshihara Y, et al. 2012. Biochem Biophys Res Cmmun. 421:57. PubMed
  17. Titus S, et al. 2013. Sci Transl Med. 13:21. PubMed
  18. Crown KN, et al. 2013. G3. 6:1927. PubMed
  19. Schenkwein D, et al. 2013. Nucleic Acids Res. 41:e61. PubMed
  20. Zhadanova NS, et al. 2014. Mol Cell Biol. 34:2786. PubMed
  21. Horrell SA, et al. 2014. Eukaryot Cell. 13:1300. PubMed
  22. Maya-Mendoza A, et al. 2015. Mol Oncol. 9:601. PubMed
Product Citations
  1. Stopfer LE, et al. 2020. Nat Commun. 2760:11. PubMed
  2. Castro M, et al. 2017. Antioxidants (Basel). 10.3390/antiox6030058. PubMed
  3. Zhang M, et al. 2011. Cancer Res. 71:7155. PubMed
  4. Fichtman B, et al. 2019. Nat Commun. 10:605. PubMed
  5. de Groot S, et al. 2020. Nat Commun. 11:3083. PubMed
  6. Pond KW, et al. 2019. PLoS Genet. 15:e1007942. PubMed
  7. Lee Y, et al. 2022. Sci Adv. 8:eabm7688. PubMed
  8. Picard E, et al. 2019. Oncoimmunology. 8:e1527498. PubMed
  9. Prasad CB, et al. 2017. Sci Rep. 7:12876. PubMed
  10. Fabián-Morales E, et al. 2021. Front Psychiatry. 12:753562. PubMed
  11. Heo J, et al. 2013. J Gerontol A Biol Sci Med Sci. 68:914. PubMed
  12. McGee-Lawrence M, et al. 2011. Bone. 48:1117. PubMed
  13. Furia L, et al. 2013. Cytometry A. 83:344. PubMed
  14. Nemcakova I, et al. 2020. Sci Rep. 10:9456. PubMed
  15. Chen C, et al. 2020. Cell Rep. 2136:30. PubMed
  16. Kopova I, et al. 2015. PLoS One. 10:123680. PubMed
  17. Becker M, et al. 2014. Cell Death Dis. 5:1000. PubMed
  18. Furia L, et al. 2022. Int J Mol Sci. 23:. PubMed
  19. Leone S, et al. 2010. Cancer Lett. 295:167. PubMed
  20. Carraro C, et al. 2022. Elife. 11:. PubMed
  21. Wang ZJ, et al. 2021. Neuropsychopharmacology. 46:1617. PubMed
RRID
AB_528914 (BioLegend Cat. No. 613405) AB_2248011 (BioLegend Cat. No. 613406)

Antigen Details

Structure
Basal histone, H2 histone family; 14 kD
Distribution

Nuclear

Function
Phosphorylated H2AX promotes DNA repair and maintains genomic stability. Important for recombination between immunoglobulin switch regions
Modification
Phosphorylation on Ser139 after double-stranded DNA breaks
Biology Area
Cell Biology, Chromatin Remodeling/Epigenetics, DNA Repair/Replication, Neuroscience
Molecular Family
Phospho-Proteins
Antigen References

1. Mannironi C, et al.1989. Nucleic Acids Res. 17:9113.
2. Celeste A, et al. 2002. Science 296:922.
3. Bassing CH, et al. 2002. Proc. Natl. Acad. Sci. USA 99:8173.
4. Reina-San-Martin B, et al. 2003. J. Exp. Med. 197:1767.

Regulation
Synthesized in G1 and S-phase of cell cycle
Gene ID
3014 View all products for this Gene ID
UniProt
View information about Phosphorylated H2A.X on UniProt.org

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