ACSL4 Rabbit Monoclonal Antibody

ACSL4 Rabbit Monoclonal Antibody

Cat: AMRe21426
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:ACSL4
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
ACSL4 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
ACSL4
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı ACSL4 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 ACSL4
Alternatif İsimler Long-chain-fatty-acid--CoA ligase 4;Long-chain acyl-CoA synthetase 4;LACS 4;
Gen Kimliği 2182
SwissProt Kimliği O60488
İmmünojen Recombinant protein of human FACL4
Uygulama
Uygulama WB,IHC,ICC/IF,ELISA,IP
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:200-1:2000,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200
Moleküler Ağırlık Calculated MW:78kD;Observed MW:78kD
Araştırma Alanı
Arka Plan
Cell localization:Membrane.The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the cognitive disability or Alport syndrome. Alternative splicing of this gene generates multiple transcript variants. [provided by RefSeq, Jan 2016]
   💬 WhatsApp