Pyruvate Dehydrogenase E1 alpha Rabbit Monoclonal antibody

Pyruvate Dehydrogenase E1 alpha Rabbit Monoclonal antibody

Cat: AMRe03791
Beden:50μL Fiyat:$158 $99_x000D_
Beden:100μL Fiyat:$288 $180_x000D_
Uygulama:WB,ICC/IF,IP
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:PDHA1
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , ,
Pyruvate Dehydrogenase E1 alpha Rabbit Monoclonal antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,ICC/IF,IP
Reaktivite
Human,Mouse,Rat
Gen Adı
PDHA1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Pyruvate Dehydrogenase E1 alpha Rabbit Monoclonal antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Monoclonal Antibody
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Saflaştırma Affinity Purified
Antijen Bilgisi
Gen Adı PDHA1
Alternatif İsimler mitochondrial; ODPA_HUMAN; PDH; PDHA; PDHA1; PDHCE1A; PDHE1 A type I; PDHE1-A type I; PHE1A; Pyruvate Dehydrogenase (lipoamide) alpha 1; Pyruvate dehydrogenase complex; E1 alpha polypeptide 1; Pyruvate Dehydrogenase E1 alpha; Pyruvate dehydrogenase E1 component subunit alpha; Pyruvate dehydrogenase E1 component subunit alpha; somatic form; mitochondrial; somatic form.
Gen Kimliği 5160
SwissProt Kimliği P08559
İmmünojen A synthetic peptide of human Pyruvate Dehydrogenase E1-alpha subunit
Uygulama
Uygulama WB,ICC/IF,IP
Seyreltme Oranı WB 1:500-1:1000,ICC/IF 1:50-1:200,IP 1:20-1:50
Moleküler Ağırlık Calculated MW: 43 kDa; Observed MW: 43 kDa
Araştırma Alanı
Signal Transduction
Arka Plan
The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). Catalyzes the removal of CO2 from pyruvate. Mutations in the α subunits of pyruvate dehydrogenase (E1) lead to congenital defects that are usually associated with lactic acidosis, neurodegeneration and early death.
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