Product nameAnti-Mre11 antibody
See all Mre11 primary antibodies
DescriptionRabbit polyclonal to Mre11
Tested applicationsSuitable for: IHC-P, WB, IP, ICC/IFmore details
Species reactivityReacts with: Human
Predicted to work with: Mouse, Rat
- Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate; A431 (Human epithelial carcinoma cell line) Whole Cell Lysate;
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Storage bufferPreservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS. pH 7.4
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab33125 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|IHC-P||1/250. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.|
|WB||Use a concentration of 1 µg/ml. Detects a band of approximately 81 kDa (predicted molecular weight: 81 kDa).|
|IP||Use at an assay dependent concentration.|
FunctionComponent of the MRN complex, which plays a central role in double-strand break (DSB) repair, DNA recombination, maintenance of telomere integrity and meiosis. The complex possesses single-strand endonuclease activity and double-strand-specific 3'-5' exonuclease activity, which are provided by MRE11A. RAD50 may be required to bind DNA ends and hold them in close proximity. This could 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. The complex may also be required for DNA damage signaling via activation of the ATM kinase. In telomeres the MRN complex may modulate t-loop formation.
Involvement in diseaseDefects in MRE11A are a cause of ataxia telangiectasia-like disorder (ATLD) [MIM:604391]. ATLD is a disease with the same clinical feature than ataxia-telangiectasia but with a somewhat milder clinical course.
Sequence similaritiesBelongs to the MRE11/RAD32 family.
modificationsPhosphorylated upon DNA damage, probably by ATM or ATR.
Cellular localizationNucleus. Localizes to discrete nuclear foci after treatment with genotoxic agents.
- Information by UniProt
- AT like disease antibody
- Ataxia telangiectasia disorder like antibody
- ATLD antibody
All lanes : Anti-Mre11 antibody (ab33125) at 1 µg/ml
Lane 1 :
Jurkat whole cell lysate (ab7899)
Lane 2 :
A431 whole cell lysate (ab7909)
Lysates/proteins at 20 µg per lane.
All lanes : IR Dye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/15000 dilution
Performed under reducing conditions.
Predicted band size: 81 kDa
Observed band size: 81 kDa
Additional bands at: 49 kDa. We are unsure as to the identity of these extra bands.
Mre11 was immunoprecipitated using 0.5mg A431 whole cell extract, 5µg of Rabbit polyclonal to Mre11 and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, A431 whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab33125.
Secondary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
Band: 81kDa: Mre11
ab33125 (1/200) stainning Mre11 in assynchronous HeLa cells (green). Cells were fixed using paraformaldehyde and counterstained with DAPI in order to highlight the nucleus. Please refer to abreview for further experimental details.
This product has been referenced in:
- Eryilmaz M et al. Localization Microscopy Analyses of MRE11 Clusters in 3D-Conserved Cell Nuclei of Different Cell Lines. Cancers (Basel) 10:N/A (2018). Human . Read more (PubMed: 29361783) »
- Forment JV et al. Genome-wide genetic screening with chemically mutagenized haploid embryonic stem cells. Nat Chem Biol 13:12-14 (2017). Read more (PubMed: 27820796) »