C2 Rabbit Monoclonal Antibody

C2 Rabbit Monoclonal Antibody

Cat: AMRe86565
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB
Reaktivite:Human,Mouse
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:C2
Category: 組換えモノクローナル抗体 Tags: , , , , ,
C2 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB
Reaktivite
Human,Mouse
Gen Adı
C2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı C2 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse
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 C2
Alternatif İsimler CO2; ARMD14
Gen Kimliği 717
SwissProt Kimliği P06681
İmmünojen A synthetic peptide of human C2
Uygulama
Uygulama WB
Seyreltme Oranı WB 1:500-1:2000
Moleküler Ağırlık Calculated MW:83 kDa; Observed MW:100 kDa
Araştırma Alanı
Arka Plan
Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]
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