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Home Antibody All anti-MRE11 antibodies

Anti-MRE11 Antibody

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Specifications Citations Related Products Product Documents
SKU Description Amount Price Availability*  
TA319245
  • Rabbit polyclonal anti-Mre11 antibody
100ug 325 3-7 Days
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IP(1)

OriGene Data

ImmunogenThis affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to amino acids 578-590 of Saccharomyces cerevisiae (baker's yeast) Mre11 protein.
Clone Name IsotypeIgG
Species ReactivitySaccharomyces cerevisiae Concentration1.19 mg/mL
Guaranteed Application *IP Suggested DilutionsELISA: 1:10,000 - 1:50,000, WB: 1:500- 1:2,000
Buffer0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Note Mre11 (also known as double-strand break repair protein MRE11) is a subunit of a complex with Rad50 and Xrs2 (RMX complex) that functions in repair of DNA double-strand breaks and in telomere stability.  Mre11 possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity that appears to be required for RMX function.  This nuclear protein is widely conserved and is also involved in meiotic double strand break processing.

Reference Data

Target NameHomo sapiens MRE11 meiotic recombination 11 homolog A (S. cerevisiae) (MRE11A), transcript variant 2
Alternative NameATLD; HNGS1; MRE11; MRE11B
Database LinkNP_005581
Function
Related PathwayStem cell - PluripotencyDruggable Genome Homologous recombinationNon-homologous end-joining

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* OriGene provides validated application data and protocol, with money back guarantee.

IP Image
Chromatin Immunoprecipitation (ChIP) using Affinity Purified Mre11 (S. cerevisiae) antibody. A yeast strain containing the HO endonuclease gene controlled by a galactose-inducible promoter (uninduced 0 m lanes) was shifted into galactose containing medium (induced 60 m lanes). After 1 hour of induction cells were cross-linked with formaldehyde followed by preparation of sheared chromatin. Chromatin was immunoprecipitated with the antibody at the stated dilutions. Immunocomplexes were captured using polyacrylamide bead linked secondary antibodies. The resultant immunoprecipitate was probed by multiplex PCR, using primers 20 bp from the MAT locus double strand break (lower arrow) and 67 kb from the break (upper band, control locus). PCR products were displayed on a polyacrylamide gel, stained with SyBR Green® (Invitrogen), and detected using a Fuji scanning fluorometer. Personal Communication. Michael Lichten, NIH, CCR, Bethesda, MD.

 

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