HNF-4α Rabbit Monoclonal Antibody

HNF-4α Rabbit Monoclonal Antibody

Cat: AMRe21100
Boyut:50μL Fiyat:$128_x000D_
Boyut:100μL Fiyat:$230_x000D_
Boyut:200μL Fiyat:$380_x000D_
Uygulama:WB,IHC,ICC/IF,ELISA,IP
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:HNF4A
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
HNF-4α Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,ELISA,IP
Reaktivite
Human,Mouse,Rat
Gen Adı
HNF4A
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı HNF-4α Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG,Kappa
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 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%protective protein
Saflaştırma Protein A
Antijen Bilgisi
Gen Adı HNF4A
Alternatif İsimler HNF4A;HNF4;NR2A1;TCF14;Hepatocyte nuclear factor 4-alpha;HNF-4-alpha;Nuclear receptor subfamily 2 group A member 1;Transcription factor 14;TCF-14;Transcription factor HNF-4
Gen Kimliği 3172
SwissProt Kimliği P41235
İmmünojen A synthetic peptide of human HNF-4-alpha
Uygulama
Uygulama WB,IHC,ICC/IF,ELISA,IP
Seyreltme Oranı WB 1:2000-1:10000,IHC 1:1000-1:5000,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
Moleküler Ağırlık Calculated MW:53kD;Observed MW:53kD
Araştırma Alanı
Arka Plan
Cell localization:Nucleus..The protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012],
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