Alkyl-DHAP synthase Rabbit Monoclonal Antibody

Alkyl-DHAP synthase Rabbit Monoclonal Antibody

Cat: AMRe86521
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,FC
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Alkyl-DHAP synthase
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,
Alkyl-DHAP synthase Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,FC
Reaktivite
Human,Mouse,Rat
Gen Adı
Alkyl-DHAP synthase
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Alkyl-DHAP synthase 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 Alkyl-DHAP synthase
Alternatif İsimler ADAS; ADPS; RCDP3; ADAP-S; ADHAPS; ALDHPSY
Gen Kimliği 8540
SwissProt Kimliği O00116
İmmünojen Recombinant protein of human Alkyl-DHAP synthase
Uygulama
Uygulama WB,IHC,FC
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:50-1:100,FC 1:10-1:100
Moleküler Ağırlık Calculated MW:73 kDa; Observed MW:73 kDa
Araştırma Alanı
Arka Plan
This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome. [provided by RefSeq, Jul 2008]
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