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Rabbit Polyclonal Phospho-FANCG (S383) antibody (STJ90615)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:40000;
Recommended protocols: check protocols
Click or hover above images to see image description for FANCG (phospho Ser383) Polyclonal Antibody.
Check alternative names for the antibodyExpand
FANCG antibody, XRCC9 antibody,|DNA repair protein XRCC9 antibody|FAG antibody|FANCG antibody|FANCG_HUMAN antibody|Fanconi anaemia complementation group G antibody|Fanconi anemia group G protein antibody|Protein FACG antibody|X ray repair, complementing defective, in Chinese hamster cells 9 antibody|X-ray repair, complementing defective, in Chinese hamster, 9 antibody|XRCC9 antibody|Anti-FANCG antibody (ab54645)
SCBT cat No: sc-100740|sc-393382|sc-28219|
FANCG (phospho Ser383) Polyclonal Antibody
|Catalogue No.|| |
Phospho-FANCG (S383) Polyclonal Antibody detects endogenous levels of FANCG protein only when phosphorylated at S383.
Synthesized phospho-peptide derived from FANCG (phospho Ser383) at AA range 330-410
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:40000;
|Molecular weight|| |
FANCG (phospho Ser383) Antibody was tube-contained. Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
FANCG (phospho Ser383) Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Fanconi anemia group G protein antibody, Protein FACG antibody, DNA repair protein XRCC9 antibody
|Protein names|| |
Fanconi anemia group G protein , Protein FACG , DNA repair protein XRCC9
|Protein function|| |
DNA repair protein that may operate in a postreplication repair or a cell cycle checkpoint function. May be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. Candidate tumor suppressor gene.
|Protein tissue specificity|| |
Highly expressed in testis and thymus. Found in lymphoblasts.
|Involvement in disease|| |
Fanconi anemia complementation group G (FANCG) [MIM:614082]: A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Contains 4 TPR repeats.
|Protein cellular localization|| |
Nucleus / Cytoplasm
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St John’s Laboratory Ltd.
|Product type|| |
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