REV1 Antibody

Code CSB-PA883372XA01HU
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) REV1 Polyclonal antibody
Uniprot No.
Target Names
REV1
Alternative Names
AIBP 80 antibody; AIBP80 antibody; Alpha integrin binding protein 80 antibody; Alpha integrin-binding protein 80 antibody; DNA repair protein REV 1 antibody; DNA repair protein REV1 antibody; FLJ21523 antibody; MGC163283 antibody; MGC26225 antibody; REV 1 (yeast homolog) like antibody; REV 1 antibody; REV 1 homolog antibody; REV 1 like antibody; REV 1 protein antibody; REV 1L antibody; REV1 (yeast homolog) like antibody; REV1 antibody; REV1 homolog (S. cerevisiae) antibody; REV1 homolog antibody; REV1 like (yeast) antibody; REV1 like antibody; Rev1 like terminal deoxycytidyl transferase antibody; REV1 protein antibody; Rev1-like terminal deoxycytidyl transferase antibody; REV1_HUMAN antibody; REV1L antibody
Raised in
Rabbit
Species Reactivity
Homo sapiens (Human)
Immunogen
Recombinant Homo sapiens (Human) REV1 protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, WB (ensure identification of antigen)
Protocols
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Value-added Deliverables
① 200ug * antigen (positive control);
② 1ml * Pre-immune serum (negative control);
Quality Guarantee
① Antibody purity can be guaranteed above 90% by SDS-PAGE detection;
② ELISA titer can be guaranteed 1: 64,000;
③ WB validation with antigen can be guaranteed positive;
Lead Time
Made-to-order (14-16 weeks)

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Target Background

Function
Deoxycytidyl transferase involved in DNA repair. Transfers a dCMP residue from dCTP to the 3'-end of a DNA primer in a template-dependent reaction. May assist in the first step in the bypass of abasic lesions by the insertion of a nucleotide opposite the lesion. Required for normal induction of mutations by physical and chemical agents.
Gene References into Functions
  1. These data indicate that dysregulation of cellular Rev1 levels leads to the accumulation of mutations and suppression of cell death, which accelerates the tumorigenic activities of DNA-damaging agents. PMID: 28498946
  2. The data directly show that, in the human genome, DNA Pol-eta and Rev1 bypass cyclobutane pyrimidine dimers and 6-4PP at replication forks, while only 6-4PP are also tolerated by a Rev3L-dependent gap-filling mechanism, independent of S phase. PMID: 27095204
  3. the catalytic function of REV1 is moderately or slightly altered by at least nine genetic variations, and the G4 DNA processing function of REV1 is slightly enhanced by the N373S variation, which might provide the possibility that certain germline missense REV1 variations affect the individual susceptibility to carcinogenesis by modifying the capability of REV1 for replicative bypass past DNA lesions and G4 motifs derived PMID: 26914252
  4. REV1 can promote PCNA monoubiquitylation after UV radiation through interacting with ubiquitylated RAD18. PMID: 26795561
  5. Saccharomyces cerevisiae PMID: 26903512
  6. Rev1 is indispensable for Translesion synthesis mediated by Poleta, Poliota, and Polkappa but is not required for TLS by Polzeta. PMID: 26680302
  7. Data suggest Rev1 protein recognition mechanism by Fanconi anemia-associated protein 20 (FAAP20). PMID: 26318859
  8. show that REV1 is a novel binding partner of the tumor suppressor p53 and regulates its activity PMID: 25614517
  9. Our results suggest for the first time that REV1 and REV3L SNPs might serve as potential predictive markers of outcome of cisplatin-based chemotherapy PMID: 24956248
  10. Structural studies suggest the possible involvement of XRCC1 and its associated repair factors, REV1 in post replication repair. PMID: 24409475
  11. The results show that human Rev1 disrupts G4 DNA structures and prevents refolding in vitro. PMID: 24366879
  12. the first structural insights into the regulation of human Rev1 for TLS polymerases. PMID: 23220741
  13. Rev1 but not Poleta depletion is epistatic to the lack of PCNA ubiquitination. PMID: 23761444
  14. a structural basis for understanding the recognition of the Rev1-CT by Y-family DNA polymerases PMID: 22691049
  15. Findings indicate that miR-96 regulates DNA repair and chemosensitivity by repressing RAD51 and REV1. PMID: 22761336
  16. Results suggest that abasic sites might be bypassed by single B- and Y-family pols or combinations, possibly by REV1 and pols iota, eta, and delta/PCNA at the insertion step opposite the lesion and by pols eta and delta/PCNA at the subsequent extension step. PMID: 20888339
  17. REV7 subunit of pol zeta mediated the interaction between REV3 and the REV1 C terminus. PMID: 22303021
  18. FAAP20 binding stabilizes Rev1 nuclear foci and promotes interaction of the Fanconi anemia core with PCNA-Rev1 DNA damage bypass complexes. PMID: 22266823
  19. Hsp90 promotes folding of REV1 into a stable and/or functional form(s) to bind to monoubiquitinated proliferating cell nuclear antigen in the regulation of translesion DNA synthesis-mediated mutagenesis PMID: 21690293
  20. WRN facilitates REV1-dependent translesion synthesis. PMID: 20691646
  21. the interaction between REV7 and REV3 creates a structural interface for REV1 binding PMID: 20164194
  22. REV1 and Polzeta facilitate repair of interstrand cross-links independently of PCNA monoubiquitination and Poleta, whereas RAD18 plus Poleta, REV1, and Polzeta are all necessary for replicative bypass of cisplatin intrastrand DNA cross-links. PMID: 20028736
  23. The results suggest that the positive charge on R357 could prevent interaction of REV1 with dGTP. PMID: 20059978
  24. UV-induced mutant frequencies at the HPRT locus were reduced up to 75% in cells with reduced levels of REV1 mRNA and data support that targeting the mutagenic translesion DNA replication pathway can greatly reduce the frequency of induced mutations. PMID: 12930947
  25. REV1 interacts with three Y-family DNA polymerases. PMID: 15189446
  26. REV1 interacts with pol eta in translesion synthesis of damaged DNA PMID: 15380106
  27. REV1-dependent processes are important determinants of cisplatin-induced genomic instability and the development of resistance. PMID: 16495473
  28. a novel biochemical activity of human REV1 protein, due to higher affinity for single-stranded DNA (ssDNA) than the primer terminus PMID: 16803901
  29. Rev1 is a polypeptide associated with Poleta. The study results suggest that arrested replication forks strengthen interactions among Poleta, Rad18/Rad6 and Rev1, consistent with the requirement for effective TLS by Poleta at sites of DNA lesions. PMID: 16824193
  30. Results support Phe257Ser and Ser257Ser genotypes are associated with a decreased risk for cervical carcinoma, while Asn373Ser and Ser373Ser genotypes increased the risk. PMID: 18470628
  31. Data show that PCNA ubiquitination and REV1 play distinct roles in the coordination of DNA damage bypass that are temporally separated relative to replication fork arrest. PMID: 18498753
  32. human REV1, apparently the slowest Y family polymerase, is kinetically highly tolerant to N(2)-adduct at G but not to O(6)-adducts. PMID: 18591245
  33. plays a role in mutagenesis and translesin DNA synthesis. (review) PMID: 18975621
  34. Poleta-REV1 interactions prevent spontaneous mutations, probably by promoting accurate translesion DNA synthesis past endogenous DNA lesions PMID: 19157994
  35. Novel structural features are important for providing Rev1 greater latitude in promoting efficient and error-free translesion DNA synthesis through the diverse array of bulky and potentially carcinogenic N(2)-deoxyguanosine DNA adducts in human cells. PMID: 19464298

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Subcellular Location
Nucleus.
Protein Families
DNA polymerase type-Y family
Tissue Specificity
Ubiquitous.
Database Links

HGNC: 14060

OMIM: 606134

KEGG: hsa:51455

STRING: 9606.ENSP00000258428

UniGene: Hs.443077

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