SOD2 Rabbit Monoclonal Antibody

SOD2 Rabbit Monoclonal Antibody

Cat: AMRe21462
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:SOD2
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
SOD2 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
SOD2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı SOD2 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 SOD2
Alternatif İsimler SOD2;Superoxide dismutase [Mn], mitochondrial
Gen Kimliği 6648
SwissProt Kimliği P04179
İmmünojen A synthetic peptide of human SOD2
Uygulama
Uygulama WB,IHC,ICC/IF,ELISA,IP
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:200-1:1000,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
Moleküler Ağırlık Calculated MW:25kD;Observed MW:22kD
Araştırma Alanı
Arka Plan
Cell localization:Mitochondrion matrix.This gene is a member of the iron/manganese superoxide dismutase family. It encodes a mitochondrial protein that forms a homotetramer and binds one manganese ion per subunit. This protein binds to the superoxide byproducts of oxidative phosphorylation and converts them to hydrogen peroxide and diatomic oxygen. Mutations in this gene have been associated with idiopathic cardiomyopathy (IDC), premature aging, sporadic motor neuron disease, and cancer. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. [provided by RefSeq, Apr 2016],
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