SYN1 Mouse Monoclonal Antibody

SYN1 Mouse Monoclonal Antibody

Cat: AMM81677
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC,ELISA,FC
Reaktivite:Human,Mouse,Monkey,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:SYN1
Category: マウスモノクローナル抗体 Tags: , , , , , , , , , , ,
SYN1 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC,ELISA,FC
Reaktivite
Human,Mouse,Monkey,Rat
Gen Adı
SYN1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı SYN1 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human,Mouse,Monkey,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG1
Klonalite Monoclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Purified antibody in PBS with 0.05% sodium azide
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı SYN1
Alternatif İsimler SYNI; SYN1a; SYN1b
Gen Kimliği 6853
SwissProt Kimliği P17600
İmmünojen Purified recombinant fragment of human SYN1 (AA: 362-511) expressed in E. Coli.
Uygulama
Uygulama WB,IHC,ICC,ELISA,FC
Seyreltme Oranı WB 1:500-1:2000,IHC 1:200-1:1000,ICC 1:200-1:1000,ELISA 1:5000-1:20000,FC 1:200-1:400
Moleküler Ağırlık 74.1kDa
Araştırma Alanı
Arka Plan
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
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