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Each lot of this antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 10 μl per 5 ml antibody dilution buffer for each mini-gel. It is recommended that the reagent be titrated for optimal performance for each application.
COA:
Hela nuclear extract was resolved by electrophoresis, transferred to nitrocellulose, and probed with rabbit anti-Fanconi D2 (Ser222) antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system. Lane 1, control cells. Lane 2, Hela cells exposed to 10 Gy radiation harvested at 2 hrs.
Fanconi anemia (also known as Fanconi anemia complementation group D2 (FANCD2)) is a 166 kD member of Fanconi anemia complementation group D. There are multiple isoforms of this nuclear protein including a post-translationally modified form. Activated FANCD2 co-localizes with BRCA1 in ionizing radiation-induced foci and in synaptonemal complexes of meiotic chromosomes. This protein is critical for cellular resistance to DNA cross-linking and cell-cycle arrest after ionizing radiation. DNA damage leads to monoubiquitination of FANCD2 and targeting to nuclear foci. Monoubiquitination occurs during normal cell cycle progression and is required for RAD51 and BRCA1 binding. This protein forms a complex with Fanconi proteins A, C, F, and G. FANCD2 has also been shown to bind to BRCA1, NBS1, and RAD51. The Poly6180 antibody recognizes the phosphorylated human FANCD2 protein (Ser222) and has been shown to be useful for Western blotting.
Other Names:
Fanconi anemia complementation group D2 (FANCD2)
Structure:
Fanconi anemia complementation group D. Multiple isoforms, post-translationally modified form, 166 kD
Distribution:
Nuclear protein, activated FANCD2 colocalizes with BRCA1 in ionizing radiation-induced foci and in synaptonemal complexes of meiotic chromosomes
Function:
Critical for cellular resistance to DNA cross-linking and cell-cycle arrest after ionizing radiation
Regulation:
DNA damage leads to monoubiquitination of FANCD2 and targeting to nuclear foci. Monoubiquitination occurs during normal cell cycle progression and is required for RAD51 and BRCA1 binding
Modification:
Phosphorylation, Ubiquitination
Interaction:
Forms a complex with Fanconi proteins A, C, F, and G; binds to BRCA1, NBS1, RAD51
Antigen References:
1. Timmers C, et al. 2001. Mol. Cell 7:241. 2. Gordon S, et al. 2003. Blood 102:136. 3. Taniguchi T, et al. 2002. Blood 100:2414. 4. Nakanishi K, et al. 2002. Nat. Cell. Biol. 4:913.
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Purified anti-Fanconi anemia D2 Phospho (Ser222)
Hela nuclear extract was resolved by electrophoresis, transferred to nitrocellulose, and probed with rabbit anti-Fanconi D2 (Ser222) antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system. Lane 1, control cells. Lane 2, Hela cells exposed to 10 Gy radiation harvested at 2 hrs.
