RASA1 Antikörper (AA 140-220)

Produktnummer ABIN3022297

Produktdetails anti-RASA1 Antikörper

Target: RASA1 (RAS P21 Protein Activator (GTPase Activating Protein) 1 (RASA1))

Bindungsspezifität: AA 140-220

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RASA1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: PPYLPPLGAG LGTVDEGDSL DGPEYEEEEV AIPLTAPPTN QWYHGKLDRT IAEERLRQAG KSGSYLIRES DRRPGSFVLS F

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 140-220 of human RASA1 (NP_002881.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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.

Handhabung: Avoid freeze / thaw cycles

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu RASA1

Target: RASA1 (RAS P21 Protein Activator (GTPase Activating Protein) 1 (RASA1))

Andere Bezeichnung: RASA1 (RASA1 Produkte)

Synonyme: CG9209 antikoerper, D-RasGAP antikoerper, Dmel\\CG9209 antikoerper, RAS-GAP antikoerper, RasGAP antikoerper, RasGap antikoerper, rasGap antikoerper, CM-AVM antikoerper, CMAVM antikoerper, GAP antikoerper, PKWS antikoerper, RASA antikoerper, RASGAP antikoerper, p120GAP antikoerper, p120RASGAP antikoerper, GAPX antikoerper, Rasa antikoerper, Gap antikoerper, vacuolar peduncle antikoerper, RAS p21 protein activator 1 antikoerper, vap antikoerper, RASA1 antikoerper, Rasa1 antikoerper

Hintergrund: The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues.,RASA1,CM-AVM,CMAVM,GAP,PKWS,RASA,RASGAP,p120,p120GAP,p120RASGAP,Cancer,Signal Transduction,G protein signaling,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Immunology & Inflammation,B Cell Receptor Signaling Pathway,RASA1

Molekulargewicht: 58 kDa/100 kDa/101 kDa/116 kDa

Gen-ID: 5921

UniProt: P20936

Pathways: Regulation of Actin Filament Polymerization, Signaling of Hepatocyte Growth Factor Receptor, VEGFR1 Specific Signals