PMS2 Mouse Monoclonal Antibody

PMS2 Mouse Monoclonal Antibody

Cat: AMM82537
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ELISA,FC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:PMS2
Category: マウスモノクローナル抗体 Tags: , , , , , , ,
PMS2 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ELISA,FC
Reaktivite
Human
Gen Adı
PMS2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı PMS2 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 PMS2
Alternatif İsimler MLH4; PMSL2; HNPCC4; PMS2CL
Gen Kimliği 5395
SwissProt Kimliği P54278
İmmünojen Purified recombinant fragment of human PMS2 (AA: (431-580)) expressed in E. Coli.
Uygulama
Uygulama WB,IHC,ELISA,FC
Seyreltme Oranı WB 1:500-1:2000,IHC 1:200-1:1000,ELISA 1:5000-1:20000,FC 1:200-1:400
Moleküler Ağırlık 95.8kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and homologous recombination. This protein forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer. The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers, and is necessary for removal of the mismatched DNA. There is a DQHA(X)2E(X)4E motif found at the C-terminus of the protein encoded by this gene that forms part of the active site of the nuclease. Mutations in this gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC; also known as Lynch syndrome) and Turcot syndrome.
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