Western Blot: BRIP1/FANCJ Antibody (pp15-IB4) [NB100-189] - Used to detect BRIP1/FANCJ in 293 cell lysate.
Immunohistochemistry-Paraffin: BRIP1/FANCJ Antibody (pp15-IB4) [NB100-189] - Analysis of a FFPE tissue section of the human breast cancer using 1:200 dilution of BRIP1/FANCJ antibody (NB100-189). The signal was ...read more
The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Theoretical MW
130 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
Ascites
Preservative
0.05% Sodium Azide
Purity
Unpurified
Alternate Names for BRIP1/FANCJ Antibody (pp15-IB4) - BSA Free
ATP-dependent RNA helicase BRIP1
BACH1
BACH1BRCA1/BRCA2-associated helicase 1
BRCA1 interacting protein C-terminal helicase 1
BRCA1-associated C-terminal helicase 1
BRCA1-binding helicase-like protein BACH1
BRCA1-interacting protein 1
BRCA1-interacting protein C-terminal helicase 1
BRIP1
EC 3.6.1
EC 3.6.4.13
FACJ
FANCJ
FANCJFanconi anemia group J protein
FLJ90232
MGC126521
MGC126523
OF
Protein FACJ
Background
FANCJ (Fanconi anemia group J protein) was originally identified as a protein which binds BRCT domains of BRCA1 and was named BACH1 (BRCA1-Associated C-terminal Helicase1) or BRIP1 (BRCA1 Interacting Protein C-terminal Helicase1), and after its identification as a component of Fanconi anemia pathway, it was renamed as FANCJ. It is expressed ubiquitously with highest levels in testes and sub-cellularly, it localizes to the nucleus. FANCJ is a DNA-dependent ATPase with 5' to 3' DNA helicase activity which is essential for genetic and structural integrity of genome. FANCJ acts late in the Fanconi anemia pathway, after FANCD2 ubiquitination, and is implicated in repairing DNA double-strand breaks through homologous recombination in FANCJ-BRCA1 interactions dependent manner. Cell-cycle regulated phosphorylation of FANCJ is essential for BRCA1 interaction and 4Fe-4S iron-sulfur-binding is required for its helicase activity. The interaction of FANCJ with proteins including MutLalpha complex and BRCA1, suggests its importance in other pathways of DNA repair and in diseases such as colon and breast cancer. Defective FANCJ causes chromosome instability disorder Fanconi anemia complementation group J.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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