FANCG anticorps (pSer383)

N° du produit ABIN8121380

Cet anticorps Lapin Polyclonal détecte spécifiquement FANCG dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour FANCG anticorps (pSer383) (ABIN8121380)

Antigène: FANCG (Fanconi Anemia Complementation Group G (FANCG))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FANCG est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-FANCG anticorps

Épitope: pSer383

Fonction: FANCG (phospho Ser383) Antibody

Specificité: Phospho-FANCG (S383) Polyclonal Antibody detects endogenous levels of FANCG protein only when phosphorylated at S383.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized phospho-peptide around the phosphorylation site of human FANCG (phospho Ser383)

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. ELISA: 1:40000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur FANCG

Antigène: FANCG (Fanconi Anemia Complementation Group G (FANCG))

Autre désignation: FANCG

Sujet:

Synonyms: FANCG, XRCC9, Fanconi anemia group G protein, Protein FACG, DNA repair protein XRCC9

Background: 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],

Gene Name: FANCG

Protein Name: Fanconi anemia group G protein

ID gène: 2189

UniProt: O15287

Pathways: Réparation de l'ADN