CFHR5 Mouse Monoclonal Antibody

CFHR5 Mouse Monoclonal Antibody

Cat: AMM81633
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:IHC,ICC,ELISA,FC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:CFHR5
Category: マウスモノクローナル抗体 Tags: , , , , , , ,
CFHR5 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA IHC,ICC,ELISA,FC
Reaktivite
Human
Gen Adı
CFHR5
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı CFHR5 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG1
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 CFHR5
Alternatif İsimler FHR5; CFHL5; FHR-5; CFHR5D
Gen Kimliği 81494
SwissProt Kimliği Q9BXR6
İmmünojen Purified recombinant fragment of human CFHR5 (AA: 344-569) expressed in E. Coli.
Uygulama
Uygulama IHC,ICC,ELISA,FC
Seyreltme Oranı IHC 1:200-1:1000,ICC 1:200-1:1000,ELISA 1:5000-1:20000,FC 1:200-1:400
Moleküler Ağırlık 64.4kDa
Araştırma Alanı
Arka Plan
This gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation. The protein encoded by this gene has nine SCRs with the first two repeats having heparin binding properties, a region within repeats 5-7 having heparin binding and C reactive protein binding properties, and the C-terminal repeats being similar to a complement component 3 b (C3b) binding domain. This protein co-localizes with C3, binds C3b in a dose-dependent manner, and is recruited to tissues damaged by C-reactive protein. Allelic variations in this gene have been associated, but not causally linked, with two different forms of kidney disease: membranoproliferative glomerulonephritis type II (MPGNII) and hemolytic uraemic syndrome (HUS).
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