ZBTB20 Antikörper

Produktnummer ABIN7012097

Produktdetails anti-ZBTB20 Antikörper

Target: ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ZBTB20 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human ZBTB20 (NP_056457.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ZBTB20

Target: ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))

Andere Bezeichnung: ZBTB20 (ZBTB20 Produkte)

Synonyme: DPZF antikoerper, HOF antikoerper, ODA-8S antikoerper, ZNF288 antikoerper, 1300017A20Rik antikoerper, 7330412A13Rik antikoerper, A930017C21Rik antikoerper, D16Wsu73e antikoerper, Oda8 antikoerper, Zfp288 antikoerper, RGD1560387 antikoerper, zinc finger and BTB domain containing 20 antikoerper, ZBTB20 antikoerper, Zbtb20 antikoerper

Hintergrund: This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Molekulargewicht:

Observed_MW: 81 kDa

Calculated_MW: 73 kDa/81 kDa

Gen-ID: 26137

UniProt: Q9HC78