ABCA1 Mouse Monoclonal Antibody

ABCA1 Mouse Monoclonal Antibody

Cat: AMM82629
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:IHC,ICC,FC
Reaktivite:Human,Mouse,Rat,Rabbit,Monkey
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:ABCA1
Category: マウスモノクローナル抗体 Tags: , , , , , , , , , ,
ABCA1 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA IHC,ICC,FC
Reaktivite
Human,Mouse,Rat,Rabbit,Monkey
Gen Adı
ABCA1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı ABCA1 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human,Mouse,Rat,Rabbit,Monkey
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG2a
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 Purified antibody in PBS with 0.05% sodium azide
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı ABCA1
Alternatif İsimler TGD; ABC1; CERP; ABC-1; HDLDT1; HPALP1; HDLCQTL13
Gen Kimliği 19
SwissProt Kimliği O95477
İmmünojen Purified recombinant fragment of human ABCA1 (AA: 2081-2261) expressed in E. Coli.
Uygulama
Uygulama IHC,ICC,FC
Seyreltme Oranı IHC 1:100-1:500,ICC 1:200-1:1000,FC 1:200-1:400
Moleküler Ağırlık 254 kDa
Araştırma Alanı
Arka Plan
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in both alleles of this gene cause Tangier disease and familial high-density lipoprotein (HDL) deficiency.
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