BZW2 antibody (Cy3)

Catalog No. ABIN1418105

Product Details anti-BZW2 Antibody (Cy3)

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 Cy3

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BZW2

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for BZW2

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

Alternative Name: BZW2 (BZW2 Products)

Synonyms: HSPC028 antibody, MGC84347 antibody, MST017 antibody, MSTP017 antibody, 1110001I24Rik antibody, Bdm2 antibody, Hfb2 antibody, zgc:55580 antibody, basic leucine zipper and W2 domains 2 antibody, basic leucine zipper and W2 domains 2 L homeolog antibody, BZW2 antibody, bzw2.L antibody, Bzw2 antibody, bzw2 antibody

Background:

Synonyms: HSPC028, MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2, Basic leucine zipper and W2 domains 2, BZW 2, MST017, BZW2_HUMAN.

Background: 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 ID: 28969

Pathways: SARS-CoV-2 Protein Interactome