BAIAP2 antibody
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- Target See all BAIAP2 Antibodies
- BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))
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Reactivity
- Human
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Host
- Mouse
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Clonality
- Monoclonal
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Conjugate
- This BAIAP2 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)
- Characteristics
- Homo sapiens BAI1-associated protein 2 (BAIAP2), transcript variant 3
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human BAIAP2 (NP_006331) produced in HEK293T cell.
- Clone
- 1D9
- Isotype
- IgG1
- Top Product
- Discover our top product BAIAP2 Primary Antibody
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- Application Notes
- WB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100,
- Comment
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 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
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- Target
- BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))
- Alternative Name
- BAIAP2 (BAIAP2 Products)
- Background
- The protein encoded by this gene has been identified as a brain-specific angiogenesis inhibitor (BAI1)-binding protein. This adaptor protein links membrane bound G-proteins to cytoplasmic effector proteins. This protein functions as an insulin receptor tyrosine kinase substrate and suggests a role for insulin in the central nervous system. It also associates with a downstream effector of Rho small G proteins, which is associated with the formation of stress fibers and cytokinesis. This protein is involved in lamellipodia and filopodia formation in motile cells and may affect neuronal growth-cone guidance. This protein has also been identified as interacting with the dentatorubral-pallidoluysian atrophy gene, which is associated with an autosomal dominant neurodegenerative disease. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
- Molecular Weight
- 57.3 kDa
- Gene ID
- 10458
- NCBI Accession
- NM_006340
- HGNC
- 10458
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