BZW2 antibody (AA 21-292)

Catalog No. ABIN7872158

This Rabbit Polyclonal antibody specifically detects BZW2 in WB, ELISA, IHC (p) and FACS. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for BZW2 antibody (AA 21-292) (ABIN7872158)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BZW2 antibody is un-conjugated

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

Product Details anti-BZW2 Antibody

Binding Specificity: AA 21-292

Purpose: BZW2 Antibody / eIF5-mimic protein 1

Purification: Antigen affinity purified

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

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the BZW2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

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

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for BZW2

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

Alternative Name: BZW2

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.

UniProt: Q9Y6E2

Pathways: SARS-CoV-2 Protein Interactome