BZW2 antibody (AbBy Fluor® 488)
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- Target See all BZW2 Antibodies
- BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This BZW2 antibody is conjugated to AbBy Fluor® 488
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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
- Top Product
- Discover our top product BZW2 Primary Antibody
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- Application Notes
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- 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
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- 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
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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
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