SOD1 Rabbit Monoclonal Antibody

SOD1 Rabbit Monoclonal Antibody

Cat: AMRe21378
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:SOD1
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
SOD1 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
SOD1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı SOD1 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 SOD1
Alternatif İsimler SOD1;Superoxide dismutase [Cu-Zn];Superoxide dismutase 1;hSod1
Gen Kimliği 6647
SwissProt Kimliği P00441
İmmünojen Recombinant protein of human Superoxide Dismutase 1
Uygulama
Uygulama WB,IHC,ICC/IF,ELISA,IP
Seyreltme Oranı WB 1:2000-1:10000,IHC 1:100-1:500,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
Moleküler Ağırlık Calculated MW:23kD;Observed MW:15kD
Araştırma Alanı
Arka Plan
Cell localization:Cytoplasm, Nucleus.The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals inThe body.The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide.The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq, Jul 2008],
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