CHD7 Antikörper (AA 2947-2997)

Produktnummer ABIN7453314

Produktdetails anti-CHD7 Antikörper

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

Bindungsspezifität: AA 2947-2997

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CHD7 Antikörper ist unkonjugiert

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

Verwendungszweck: Rabbit anti-CHD7 Antibody, Affinity Purified

Aufreinigung: Affinity Purified

Immunogen: between AA 2947 and 2997

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise:

IP: 2 - 5 μg/mg lysate

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 200 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C

Haltbarkeit: 12 months

Details zu CHD7

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

Andere Bezeichnung: CHD7 (CHD7 Produkte)

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

Hintergrund: 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.

Gen-ID: 55636

NCBI Accession: NP_060250

UniProt: Q9P2D1

Pathways: Sensory Perception of Sound, Chromatin Binding