IQGAP3 Antikörper
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- Target Alle IQGAP3 Produkte
- IQGAP3 (IQ Motif Containing GTPase Activating Protein 3 (IQGAP3))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser IQGAP3 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human IQGAP3 (NP_839943.2).
- Isotyp
- IgG
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- Applikationshinweise
- WB 1:500-1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- IQGAP3 (IQ Motif Containing GTPase Activating Protein 3 (IQGAP3))
- Andere Bezeichnung
- IQGAP3 (IQGAP3 Produkte)
- Synonyme
- IQGAP3 antikoerper, AI593484 antikoerper, D030034H08 antikoerper, IQ motif containing GTPase activating protein 3 antikoerper, IQGAP3 antikoerper, iqgap3 antikoerper, Iqgap3 antikoerper
- Hintergrund
- IQGAP3 (IQ motif containing GTPase activating protein 3) is a 1,631 amino acid protein that acts as an effector of Cdc42 and Rac 1, linking their activation to the cytoskeleton during neuronal morphogenesis. A novel member of the IQGAP family, IQGAP3 is highly expressed in brain where it localizes to axons of hippocampal neurons. IQGAP3 contains one Ras-GAP domain, a CH (calponin-homology) domain, four IQ domains and is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson's disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
- Molekulargewicht
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Observed_MW: 170 kDa
Calculated_MW: 184 kDa
- Gen-ID
- 128239
- UniProt
- Q86VI3
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