CHD7 anticorps (AA 2947-2997)

N° du produit ABIN7453314

Détail du produit anti-CHD7 anticorps

Antigène: CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))

Épitope: AA 2947-2997

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CHD7 est non-conjugé

Application: Western Blotting (WB), Immunoprecipitation (IP)

Fonction: Rabbit anti-CHD7 Antibody, Affinity Purified

Purification: Affinity Purified

Immunogène: between AA 2947 and 2997

Isotype: IgG

Information d'application

Indications d'application:

IP: 2 - 5 μg/mg lysate

WB: 1:2,000 - 1:10,000

Restrictions: For Research Use only

Stockage

Concentration: 200 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % 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: 4 °C

Date de péremption: 12 months

Détails sur CHD7

Antigène: CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))

Autre désignation: CHD7 (CHD7 Produits)

Synonymes: anticorps CHD7, anticorps fd19h06, anticorps si:ch211-197o6.2, anticorps wu:cegs2051, anticorps wu:fb37f10, anticorps wu:fb39h04, anticorps wu:fd19h06, anticorps HH5, anticorps IS3, anticorps KAL5, anticorps A730019I05Rik, anticorps Cycn, anticorps Cyn, anticorps Dz, anticorps Edy, anticorps Flo, anticorps GENA 47, anticorps GENA 60, anticorps Gena 52, anticorps Lda, anticorps Mt, anticorps Obt, anticorps Todo, anticorps WBE1, anticorps Whi, anticorps metis, anticorps chromodomain helicase DNA binding protein 7 L homeolog, anticorps chromodomain helicase DNA binding protein 7, anticorps chd7.L, anticorps CHD7, anticorps chd7, anticorps Chd7

Sujet: Background: CHD7 is a member of the CHD (chromodomain-helicase-DNA-binding) family of proteins that interacts with nucleosomes and plays a role in chromatin remodeling to modulate transcription. The members of the CHD family of proteins possess 3 common structural and functional domains: a chromodomain (chromatin organization modifier), an SNF2-like helicase/ATPase domain, and a C-terminal DNA-binding domain. CHD7 is implicated to play a role in development. Mutations in CHD7 are associated with CHARGE syndrome, a multi-symptom syndrome characterized by congenital anomalies and malformations of the heart, inner ear, retina, and palate.

ID gène: 55636

NCBI Accession: NP_060250

UniProt: Q9P2D1

Pathways: Sensory Perception of Sound, Chromatin Binding