Phospho-FANCG (S383) Antibody (PACO02688)
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주문- SKU:
- PACO02688
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
Antibody Name: | Phospho-FANCG (S383) Antibody |
Antibody SKU: | PACO02688 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB |
Recommended Dilutions: | WB:1:500-1:2000 |
Species Reactivity: | Human |
Immunogen: | synthesized peptide derived from human FANCG around the phosphorylation site of S383. |
Form: | Liquid |
Storage Buffer: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Purification Method: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Synonyms: | FANCG; XRCC9; Fanconi anemia group G protein; Protein FACG; DNA repair protein XRCC9 |
UniProt Protein Function: | FANCG: 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. Defects in FANCG are a cause of Fanconi anemia complementation group G (FANCG). 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. |
UniProt Protein Details: | Protein type:DNA repair, damage Chromosomal Location of Human Ortholog: 9p13 Cellular Component: cytoplasm; mitochondrion; nucleolus; nucleoplasm; plasma membrane Molecular Function:damaged DNA binding; protein binding Biological Process: cell cycle checkpoint; DNA repair; mitochondrion organization and biogenesis Disease: Fanconi Anemia, Complementation Group G; Tracheoesophageal Fistula With Or Without Esophageal Atresia |
NCBI Summary: | The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G. [provided by RefSeq, Jul 2008] |
UniProt Code: | O15287 |
NCBI GenInfo Identifier: | 6136453 |
NCBI Gene ID: | 2189 |
NCBI Accession: | O15287.1 |
UniProt Related Accession: | O15287 |
Molecular Weight: | 68,554 Da |
NCBI Full Name: | Fanconi anemia group G protein |
NCBI Synonym Full Names: | Fanconi anemia complementation group G |
NCBI Official Symbol: | FANCG |
NCBI Official Synonym Symbols: | FAG; XRCC9 |
NCBI Protein Information: | Fanconi anemia group G protein |
UniProt Protein Name: | Fanconi anemia group G protein |
UniProt Synonym Protein Names: | DNA repair protein XRCC9 |
Protein Family: | Fanconi anemia group G protein |
UniProt Gene Name: | FANCG |
UniProt Entry Name: | FANCG_HUMAN |