BZW2 antibody (AA 21-292) (FITC)

Catalog No. ABIN7972127

The FITC-conjugated Rabbit Polyclonal anti-BZW2 antibody (ABIN7972127) specifically detects BZW2 in FACS. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for BZW2 antibody (AA 21-292) (FITC) (ABIN7972127)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BZW2 antibody is conjugated to FITC

Application: Flow Cytometry (FACS)

Product Details anti-BZW2 Antibody (FITC)

Binding Specificity: AA 21-292

Purpose: Anti-BZW2 Antibody FITC Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

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

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

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

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for BZW2

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

Alternative Name: BZW2

Background:

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

Gene ID: 28969

UniProt: Q9Y6E2

Pathways: SARS-CoV-2 Protein Interactome