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RASA1 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-52205

宿主: Rabbit

反应性: H,R

应用: IHC

  • 详情
  • Overview

    Synonyms CM AVM,CMAVM,DKFZp434N071,GAP,GTPase activating protein,GTPase-activating protein,OTTHUMP00000222390,OTTHUMP00000222391,OTTHUMP00000222392,OTTHUMP00000222393,p120GAP,p120RASGAP,PKWS,Ras GTPase-activating protein 1,RAS p21 protein activator (GTPase activating protein) 1,Ras p21 protein activator,RASA,RASA1,RASA1,RasGAP,Triphosphatase activating protein,RASA1抗体
    Swissprot P20936
    Source Rabbit
    Reactivity Human,Rat
    Immunogen Fusion protein of human RASA1
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:30-1:150
    Concentration 0.6mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytoplasm.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background 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.
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