BZW2 anticorps (AA 21-292) (APC)

N° du produit ABIN7972129

L’anticorps anti-BZW2 Polyclonal Lapin est utilisé pour la détection de BZW2 dans des échantillons de Humain, Souris et Rat. Il a été validé pour FACS.

Aperçu rapide pour BZW2 anticorps (AA 21-292) (APC) (ABIN7972129)

Antigène: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BZW2 est conjugé à/à la APC

Application: Flow Cytometry (FACS)

Détail du produit anti-BZW2 anticorps (APC)

Épitope: AA 21-292

Fonction: Anti-BZW2 Antibody APC Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human BZW2 recombinant protein (Position: E21-A292).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur BZW2

Antigène: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Autre désignation: BZW2

Sujet:

Background: Basic Leucine Zipper and W2 Domain-Containing Protein 2 is a protein that is encoded by the BZW2 gene. BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

Gene Full Name: basic leucine zipper and W2 domains 2

ID gène: 28969

UniProt: Q9Y6E2

Pathways: SARS-CoV-2 Protein Interactome