Recombinant Human FANCI protein (GST tag N-Terminus)
Be the first to review this product! Submit a review
|
(0 Publication)
Recombinant Human FANCI protein (GST tag N-Terminus) is a Human Fragment protein, in the 180 to 252 aa range, expressed in Wheat germ, with >80%, suitable for SDS-PAGE, ELISA, WB.
View Alternative Names
KIAA1794, FANCI, Fanconi anemia group I protein, Protein FACI
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human FANCI protein (GST tag N-Terminus) (AB132153)
SDS-PAGE analysis of ab132153 on a 12.5% gel stained with Coomassie Blue.
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The FANCI protein acts as part of the multiprotein Fanconi anemia (FA) core complex. This complex Functions in the repair of DNA interstrand crosslinks which are severe forms of DNA damage. Successful function of FANCI is important for maintaining genomic stability and subsequently proper cell cycle progression. It partners with proteins including FANCD2 to coordinate the homologous recombination repair process. Defective FANCI leads to disrupted DNA repair resulting in cellular damage and apoptosis.
Pathways
FANCI plays a major role in the Fanconi anemia pathway and the broader DNA damage response system. The FA pathway which involves over 20 proteins forms a network integral in repairing DNA crosslinks. FANCI tightly interacts with proteins like FANCD2 to initiate DNA repair in response to damage. The successful coordination of these proteins ensures the stability of genetic material throughout the cell cycle affecting cell fate decisions such as survival or apoptosis.
Specifications
Form
Liquid
Additional notes
Glutathione Sepharose
General info
Function
Plays an essential role in the repair of DNA double-strand breaks by homologous recombination and in the repair of interstrand DNA cross-links (ICLs) by promoting FANCD2 monoubiquitination by FANCL and participating in recruitment to DNA repair sites (PubMed : 17412408, PubMed : 17460694, PubMed : 17452773, PubMed : 19111657, PubMed : 36385258). The FANCI-FANCD2 complex binds and scans double-stranded DNA (dsDNA) for DNA damage; this complex stalls at DNA junctions between double-stranded DNA and single-stranded DNA (PubMed : 19589784). Participates in S phase and G2 phase checkpoint activation upon DNA damage (PubMed : 25862789).
Sequence similarities
Belongs to the Fanconi anemia group I protein family.
Post-translational modifications
Monoubiquitinated by FANCL on Lys-523 during S phase and upon genotoxic stress (PubMed:17412408, PubMed:17460694, PubMed:19589784, PubMed:36385258). Deubiquitinated by USP1 as cells enter G2/M, or once DNA repair is completed (PubMed:36385258). Monoubiquitination requires the FANCA-FANCB-FANCC-FANCE-FANCF-FANCG-FANCM complex (PubMed:17412408, PubMed:17460694). Ubiquitination is required for binding to chromatin, DNA repair, and normal cell cycle progression (PubMed:36385258). Monoubiquitination is stimulated by DNA-binding (PubMed:36385258).. Phosphorylated in response to DNA damage by ATM and/or ATR (PubMed:17412408). Phosphorylation of FANCI promotes ubiquitination of FANCD2, which prevents DNA release from the FANCI-FANCD2 complex (By similarity).
Subcellular localisation
Nucleus
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com