FANCG antibody
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
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.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Fanconi anemia, complementation group G (FANCG) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500-1:2000; IF: 1:20-1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 65-68 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| UniProt ID | O15287 |
| Gene ID | 2189 |
| Alias | Fanconi anemia group G protein (Protein FACG),DNA repair protein XRCC9,FANCG,XRCC9 |
| Background | Antibody anti-FANCG |
| Status | RUO |
| Note | Mol. Weight 65-68 kDa |
Descripción
Related Products
FANCG antibody
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.
Ver Producto
Fanconi Anemia Group G Protein (FANCG) Antibody
Fanconi Anemia Group G Protein (FANCG) Antibody is a Rabbit Polyclonal antibody against Fanconi Anemia Group G Protein (FANCG). The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, Fanconi Anemia Group G Protein (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.
Ver Producto
Fanconi Anemia Group G Protein Phospho-Ser383 (FANCG pS383) Antibody
Rabbit polyclonal antibody against Fanconi Anemia Group G Protein (FANCG) protein. Immunogen region is Internal. Specificity is as follows for the reactive species: H:S383.
Ver Producto