Lipoamide Dehydrogenase Rabbit Monoclonal Antibody

Lipoamide Dehydrogenase Rabbit Monoclonal Antibody

Cat: AMRe87348
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Lipoamide Dehydrogenase
Category: 組換えモノクローナル抗体 Tags: , , , , , , ,
Lipoamide Dehydrogenase Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC
Reaktivite
Human,Mouse,Rat
Gen Adı
Lipoamide Dehydrogenase
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Lipoamide Dehydrogenase Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
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 Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı Lipoamide Dehydrogenase
Alternatif İsimler E3; LAD; DLDD; DLDH; GCSL; PHE3; OGDC-E3
Gen Kimliği 1738
SwissProt Kimliği P09622
İmmünojen A synthetic peptide of human Lipoamide Dehydrogenase
Uygulama
Uygulama WB,IHC
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:100-1:200
Moleküler Ağırlık Calculated MW:54 kDa; Observed MW:54 kDa
Araştırma Alanı
Arka Plan
This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
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