IκB-α Rabbit Monoclonal Antibody

IκB-α Rabbit Monoclonal Antibody

Cat: AMRe21140
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:NFKBIA
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
IκB-α 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
NFKBIA
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı IκB-α 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 NFKBIA
Alternatif İsimler NF-kappa-B inhibitor alpha;I-kappa-B-alpha;IkB-alpha;IkappaBalpha;Major histocompatibility complex enhancer-binding protein MAD3;
Gen Kimliği 4792
SwissProt Kimliği P25963
İmmünojen A synthetic peptide corresponding to target protein
Uygulama
Uygulama WB,IHC,ICC/IF,ELISA,IP
Seyreltme Oranı WB 1:2000-1:10000,IHC 1:200-1:2000,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
Moleküler Ağırlık Calculated MW:36kD;Observed MW:36kD
Araştırma Alanı
Arka Plan
Cell localization:Cytoplasm, Nucleus.This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011],
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