Anti-MRE11 Antibody, clone 15B8.1E7.6

Evaluated by Western Blotting in Ramo cell lysate.

Western Blotting Analysis: 4 µg/mL of this antibody detected MRE11 in 10 µg of Ramo cell lysate.

Anti-MRE11, clone 15B8.1E7.6 , Cat. No. MABE1153, is a highly specific armenian hamster monoclonal antibody that targets Double-strand break repair protein MRE11A and has been tested in Western Blotting.

Research Category
Epigenetics & Nuclear Function

Western Blotting Analysis: 1 µg/mL from a representative lot detected MRE11 in 10 µg of mouse embryo fibroblast cell lysate (MEFs).

Clone 15B8.1E7.6 detects Double-strand break repair protein MRE11A in human and murine cells.

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Double-strand break repair protein MRE11A (UniProt: Q61216; also known as MmMRE11A, Meiotic recombination 11 homolog 1, MRE11 homolog 1, Meiotic recombination 11 homolog A, MRE11 homolog A) is encoded by the Mrer11a (also known as Mre11) gene (Gene ID: 17535) in murine species. MRE11A a nuclear protein involved in homologous recombination, telomere length maintenance, and DNA double-strand break repair. It localizes to discrete nuclear foci after treatment with genotoxic agents. MRE11A is a component of the MRN complex that possesses single-strand endonuclease activity and double-strand-specific 3′-5′ exonuclease activity. MRE11A forms a complex with the RAD50 homolog, which is required for non-homologous joining of DNA end. RAD50 may be required to bind DNA ends and hold them in close proximity, which facilitate searches for short or long regions of sequence homology in the recombining DNA templates, and may also stimulate the activity of DNA ligases and/or restrict the nuclease activity of MRE11A to prevent nucleolytic degradation past a given point. In conjunction with a DNA ligase, MRE11A is reported to promote the joining of non-complementary ends in vitro using short homologies near the ends of the DNA fragments.

~80 kDa observed; 80.22 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Recombinant fragment corresponding to 540 amino acids from murine Double-strand break repair protein MRE11A.

Concentration: Please refer to lot specific datasheet.

Replaces: PC388-100UG

Format: Purified

Protein G purified

Purified armenian hamster monoclonal antibodyIgG in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Stable for 1 year at 2-8°C from date of receipt.