BZW2 anticorps (AA 21-292)

N° du produit ABIN7872158

Cet anticorps Lapin Polyclonal détecte spécifiquement BZW2 dans WB, ELISA, IHC (p) et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour BZW2 anticorps (AA 21-292) (ABIN7872158)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BZW2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Détail du produit anti-BZW2 anticorps

Épitope: AA 21-292

Fonction: BZW2 Antibody / eIF5-mimic protein 1

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids E21-A292) was used as the immunogen for the BZW2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the BZW2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the BZW2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur BZW2

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

Autre désignation: BZW2

Sujet: 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.

UniProt: Q9Y6E2

Pathways: SARS-CoV-2 Protein Interactome