WHSC1 anticorps (AA 525-575)

N° du produit ABIN7453147

Détail du produit anti-WHSC1 anticorps

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

Épitope: AA 525-575

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WHSC1 est non-conjugé

Application: Western Blotting (WB)

Fonction: Rabbit anti-NSD2 Antibody, Affinity Purified

Purification: Affinity Purified

Immunogène: between AA 525 and 575

Isotype: IgG

Information d'application

Indications d'application:

IP: Not recommended

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 WHSC1

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

Autre désignation: NSD2 (WHSC1 Produits)

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

Sujet: Background: MMSET (multiple myeloma SET domain-containing protein) or NSD2 (nuclear SET-domain containing protein 2) is the product of the Wolf-Hirschhorn syndrome candidate 1 (WHSC1) gene. MMSET is 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 and is a probable histone methyltransferase. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4 [taken from NCBI Entrez Gene (Gene ID: 7468].

ID gène: 7468

NCBI Accession: NP_579877

UniProt: O96028

Pathways: SARS-CoV-2 Protein Interactome