Product Details

Uniprot No.

Target Names

RAD51B

Alternative Names

DNA repair protein RAD51 homolog 2 antibody; hREC2 antibody; MGC34245 antibody; OTTHUMP00000212251 antibody; OTTHUMP00000212253 antibody; OTTHUMP00000212254 antibody; OTTHUMP00000212255 antibody; R51H2 antibody; RA51B_HUMAN antibody; RAD51 homolog B (S. cerevisiae) antibody; RAD51 homolog B antibody; RAD51 like 1 antibody; RAD51 like protein 1 antibody; RAD51-like protein 1 antibody; Rad51B antibody; RAD51L1 antibody; REC2 antibody; RecA like protein antibody; Recombination repair protein antibody

Raised in

Rabbit

Species Reactivity

Human,Mouse,Rat

Immunogen

Human RAD51L1

Immunogen Species

Homo sapiens (Human)

Isotype

IgG

Purification Method

Antigen Affinity Purified

Concentration

It differs from different batches. Please contact us to confirm it.

Buffer

PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.

Tested Applications

ELISA,WB

Protocols

ELISA Protocol
Western Blotting(WB) Protocol

Troubleshooting and FAQs

Antibody FAQs

Storage

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Lead Time

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

Target Background

Function

Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. May promote the assembly of presynaptic RAD51 nucleoprotein filaments. Binds single-stranded DNA and double-stranded DNA and has DNA-dependent ATPase activity. Part of the RAD21 paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream of BRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 binds predominantly to the intersection of the four duplex arms of the Holliday junction and to junction of replication forks. The BCDX2 complex was originally reported to bind single-stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. The BCDX2 subcomplex RAD51B:RAD51C exhibits single-stranded DNA-dependent ATPase activity suggesting an involvement in early stages of the HR pathway.

Gene References into Functions

We successfully identified a common variant, rs911263, as being significantly associated with the disease status . In addition, this SNP was shown to be related to erosion, a clinical assessment of disease severity in RA (P = 2.89 x 10(-5), OR = 0.52). These findings shed light on the role of RAD51B in the onset and severity of Rheumatoid arthritis (RA). PMID: 28361912
hypermethylation of homologous recombination DNA repair genes including RAD51B and XRCC3 is associated with an inflamed phenotype in squamous cell cancers of the head and neck, lung and cervix. PMID: 27683114
our study suggested that miRNA-binding site genetic variants of RAD51B may modify the susceptibility to cervical cancer, which is important to identify individuals with differential risk for this malignancy and to improve the effectiveness of preventive intervention. PMID: 27334422
common variation is significantly associated with familial breast cancer risk PMID: 27149063
over-expression of RAD51B promoted cell proliferation, aneuploidy, and drug resistance, while RAD51B knockdown led to G1 arrest and sensitized cells to 5-fluorouracil PMID: 27651161
a novel germ line RAD51B nonsense mutation, and reduced expression of RAD51B in melanoma cells indicating inactivation of RAD51B PMID: 25600502
Mutations in epithelial ovarian cancer cases were more frequent in RAD51C (14 occurrences, 0.41%) and RAD51D (12 occurrences, 0.35%) than in RAD51B (two occurrences, 0.06%). PMID: 26261251
the risk of developing AMD exhibits dose dependency as well as an epistatic combined effect in rs17105278 T>C and rs4902566 C>T carriers and that the elevated risk for rs17105278 T>C carriers may be due to decreased transcription of RAD51B. PMID: 24526414
Relative excess risk of breast cancer due to interaction between RAD51L1 single-nucleotide polymorphism and BMI. PMID: 25255808
Data indicate that complement factor H (CFH) R1210C and common variants in COL8A1 and RAD51B plus six genes contribute predictive information for advanced macular degeneration (AMD) beyond macular and behavioral phenotypes. PMID: 24498017
It confirms that RAD51 paralog mutations confer breast and ovarian cancer predisposition and are rare events. PMID: 24139550
This study provides robust evidence for an association of rheumatoid arthritis susceptibility with genes involved in B cell differentiation (BACH2) and DNA repair (RAD51B). PMID: 24022229
SNP in RAD51B at 14q24.1 was significantly associated with male breast cancer risk PMID: 23001122
Single nucleotide polymorphism in RAD51L1 is associated with breast cancer. PMID: 22454379
our results suggest that RAD51L1 is unlikely to represent a high-penetrance breast cancer susceptibility gene. PMID: 21533530
Single Nucleotide Polymorphisms in RAD51L1 gene is associated with glioblastoma. PMID: 22017238
rs11249433 at 1p.11.2, and two highly correlated single-nucleotide polymorphisms rs999737 and rs10483813 (r(2)= 0.98) at 14q24.1 (RAD51L1), for up to 46 036 invasive breast cancer cases and 46 930 controls from 39 studies, were genotyped. PMID: 21852249
findings support the notion that DNA repair genes, in particular RAD51L1, play a role in nasopharyngeal carcinoma etiology and development PMID: 21368091
polymorphisms in and haplotypes of the RAD51L1 gene, which is involved in the double-strand break repair pathway, modulate gamma-radiation-induced mutagen sensitivity. PMID: 20610542
BCR/ABL fragments were used for identifying the sites of BCR/ABL interaction with RAD51B PMID: 19657362
involved in the frequently occurring t(6;14) (p21;q23-->q24) in pulmonary chondroid hamartomas PMID: 11978964
Rad51B protein may have a specific function in Holliday junction processing in the homologous recombinational repair pathway in humans PMID: 12441335
motif in the N-terminus of Rad51B serves as an NLS that allows Rad51B to localize to the nucleus independent of Rad51C or BRCA2 PMID: 15701685
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). PMID: 19330030