Mouse Anti-RAD50 Recombinant Antibody (CBT4759) (V2LY-0625-LY429)

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Tested Data
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Datasheet Target Q & As Review & reward Protocols Associated Products

Basic Information

Host Animal
Mouse
Clone
CBT4759
Application
WB
Immunogen
Purified recombinant fragment of human RAD50 (AA: 228-359) expressed in E. Coli.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal Antibody
Application Notes
ApplicationNote
WB1:500-1:2,000
ELISA1:10,000

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS
Preservative
Sodium azide
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.
More Infomation

Target

Full Name
RAD50 DOUBLE STRAND BREAK REPAIR PROTEIN
Entrez Gene ID
UniProt ID
Function
Component 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 MRE11. 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 MRE11 to prevent nucleolytic degradation past a given point (PubMed:11741547, PubMed:9590181, PubMed:9705271, PubMed:9651580).
The complex may also be required for DNA damage signaling via activation of the ATM kinase (PubMed:15064416).
In telomeres the MRN complex may modulate t-loop formation (PubMed:10888888).
Biological Process
Biological Process cellular response to DNA damage stimulusManual Assertion Based On ExperimentIDA:MGI
Biological Process chromosome organization involved in meiotic cell cycleManual Assertion Based On ExperimentIBA:GO_Central
Biological Process DNA double-strand break processing1 PublicationIC:ComplexPortal
Biological Process DNA duplex unwindingManual Assertion Based On ExperimentIMP:BHF-UCL
Biological Process DNA recombinationManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process DNA repairManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process DNA strand resection involved in replication fork processing1 PublicationIC:ComplexPortal
Biological Process double-strand break repairManual Assertion Based On ExperimentIMP:UniProtKB
Biological Process homologous recombination1 PublicationIC:ComplexPortal
Biological Process mitotic G2/M transition checkpoint1 PublicationIC:ComplexPortal
Biological Process negative regulation of telomere cappingManual Assertion Based On ExperimentIDA:BHF-UCL
Biological Process nucleic acid phosphodiester bond hydrolysisManual Assertion Based On ExperimentIBA:GO_Central
Biological Process positive regulation of kinase activityManual Assertion Based On ExperimentIDA:BHF-UCL
Biological Process positive regulation of protein autophosphorylationManual Assertion Based On ExperimentIDA:BHF-UCL
Biological Process positive regulation of telomere maintenanceManual Assertion Based On ExperimentIMP:BHF-UCL
Biological Process reciprocal meiotic recombinationManual Assertion Based On ExperimentTAS:ProtInc
Biological Process regulation of mitotic recombinationManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process telomere maintenanceManual Assertion Based On ExperimentTAS:BHF-UCL
Biological Process telomere maintenance via recombinationManual Assertion Based On ExperimentIBA:GO_Central
Biological Process telomere maintenance via telomeraseManual Assertion Based On ExperimentIDA:UniProtKB
Biological Process telomeric 3' overhang formationManual Assertion Based On ExperimentIMP:BHF-UCL
Cellular Location
Nucleus
Chromosome, telomere
Chromosome
Localizes to discrete nuclear foci after treatment with genotoxic agents.
Involvement in disease
Nijmegen breakage syndrome-like disorder (NBSLD):
A disorder similar to Nijmegen breakage syndrome and characterized by chromosomal instability, radiation sensitivity, microcephaly, growth retardation, short stature and bird-like face. Immunodeficiency is absent.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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