RASA1 Rabbit Monoclonal antibody

RASA1 Rabbit Monoclonal antibody

Cat: AMRe03182
Beden:50μL Fiyat:$158 $99_x000D_
Beden:100μL Fiyat:$288 $180_x000D_
Uygulama:WB,IHC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:RASA1
Category: 組換えモノクローナル抗体 Tags: , , , , , ,
RASA1 Rabbit Monoclonal antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC
Reaktivite
Human
Gen Adı
RASA1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı RASA1 Rabbit Monoclonal antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Monoclonal Antibody
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Saflaştırma Affinity Purified
Antijen Bilgisi
Gen Adı RASA1
Alternatif İsimler GAP; PKWS; RASA; p120; CMAVM; CM-AVM; CMAVM1; RASGAP; p120GAP; p120RASGAP
Gen Kimliği 5921
SwissProt Kimliği P20936
İmmünojen A synthetic peptide of human RASA1
Uygulama
Uygulama WB,IHC
Seyreltme Oranı WB 1:500-1:1000,IHC 1:50-1:100
Moleküler Ağırlık Calculated MW: 116 kDa; Observed MW: 140 kDa
Araştırma Alanı
Signal Transduction
Arka Plan
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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