WHSC1 Antikörper

Produktnummer ABIN7263985

Produktdetails anti-WHSC1 Antikörper

Target: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WHSC1 Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human WHSC1 (NP_579877.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:200

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 WHSC1

Target: WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))

Andere Bezeichnung: WHSC1 (WHSC1 Produkte)

Synonyme: WHSC1 antikoerper, fc12c04 antikoerper, wu:fc12c04 antikoerper, wu:fi20c01 antikoerper, si:rp71-77d7.2 antikoerper, whs antikoerper, nsd2 antikoerper, trx5 antikoerper, mmset antikoerper, reiibp antikoerper, MMSET antikoerper, NSD2 antikoerper, REIIBP antikoerper, TRX5 antikoerper, WHS antikoerper, RGD1565590 antikoerper, 5830445G22Rik antikoerper, 9430010A17Rik antikoerper, AW555663 antikoerper, C130020C13Rik antikoerper, D030027O06Rik antikoerper, D930023B08Rik antikoerper, Whsc1l antikoerper, mKIAA1090 antikoerper, nuclear receptor binding SET domain protein 2 antikoerper, Wolf-Hirschhorn syndrome candidate 1 antikoerper, NSD2 antikoerper, nsd2 antikoerper, WHSC1 antikoerper, Nsd2 antikoerper

Hintergrund: This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4,14)(p16.3,q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.

Gen-ID: 7468

UniProt: O96028

Pathways: SARS-CoV-2 Protein Interaktom