BAIAP2 Antikörper
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- Target Alle BAIAP2 Antikörper anzeigen
- BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser BAIAP2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
- Produktmerkmale
- Homo sapiens BAI1-associated protein 2 (BAIAP2), transcript variant 3
- Aufreinigung
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human BAIAP2(NP_005331) produced in HEK293 cell.
- Klon
- 1C10
- Isotyp
- IgG2a
- Top Product
- Discover our top product BAIAP2 Primärantikörper
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- Applikationshinweise
- WB 1:2000, IF 1:100, FLOW 1:100,
- Kommentare
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The concentration of the product may vary between diferrent lots.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
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- Target
- BAIAP2 (BAI1-Associated Protein 2 (BAIAP2))
- Andere Bezeichnung
- BAIAP2 (BAIAP2 Produkte)
- Hintergrund
- 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.
- Molekulargewicht
- 57.3 kDa
- Gen-ID
- 10458
- NCBI Accession
- NM_006340
- HGNC
- 10458
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