MLH1 Rabbit Monoclonal Antibody

MLH1 Rabbit Monoclonal Antibody

Cat: AMRe87475
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,FC,IP
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:MLH1
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,
MLH1 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,FC,IP
Reaktivite
Human
Gen Adı
MLH1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı MLH1 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
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 MLH1
Alternatif İsimler FCC2; COCA2; HNPCC; hMLH1; HNPCC2
Gen Kimliği 4292
SwissProt Kimliği P40692
İmmünojen A synthetic peptide of human MLH1
Uygulama
Uygulama WB,IHC,ICC/IF,FC,IP
Seyreltme Oranı WB 1:500-1:2000,IHC 1:50-1:200,ICC/IF 1:100-1:200,FC 1:50-1:200,IP 1:20-1:50
Moleküler Ağırlık Calculated MW:85 kDa; Observed MW:85 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene can heterodimerize with mismatch repair endonuclease PMS2 to form MutL alpha, part of the DNA mismatch repair system. When MutL alpha is bound by MutS beta and some accessory proteins, the PMS2 subunit of MutL alpha introduces a single-strand break near DNA mismatches, providing an entry point for exonuclease degradation. The encoded protein is also involved in DNA damage signaling and can heterodimerize with DNA mismatch repair protein MLH3 to form MutL gamma, which is involved in meiosis. This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). [provided by RefSeq, Aug 2017]
   💬 WhatsApp