NTH1 Rabbit Monoclonal Antibody

NTH1 Rabbit Monoclonal Antibody

Cat: AMRe85872
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,ICC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:NTH1
Category: 組換えモノクローナル抗体 Tags: , , , , ,
NTH1 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,ICC
Reaktivite
Human
Gen Adı
NTH1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı NTH1 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 Purified antibody in TBS with 0.05% sodium azide,0.05%protective protein and 50% glycerol.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı NTH1
Alternatif İsimler FAP3; NTH1; OCTS3; hNTH1
Gen Kimliği 4913
SwissProt Kimliği P78549
İmmünojen Recombinant protein of human NTH1
Uygulama
Uygulama WB,ICC
Seyreltme Oranı WB 1:500-1:1000,ICC 1:50-1:200
Moleküler Ağırlık Calculated MW: 34 kDa; Observed MW: 34 kDa
Araştırma Alanı
Arka Plan
Bifunctional DNA N-glycosylase with associated apurinic/apyrimidinic (AP) lyase function that catalyzes the first step in base excision repair (BER), the primary repair pathway for the repair of oxidative DNA damage. The DNA N-glycosylase activity releases the damaged DNA base from DNA by cleaving the N-glycosidic bond, leaving an AP site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination. Primarily recognizes and repairs oxidative base damage of pyrimidines. Has also 8-oxo-7,8-dihydroguanine (8-oxoG) DNA glycosylase activity. Acts preferentially on DNA damage opposite guanine residues in DNA. Is able to process lesions in nucleosomes without requiring or inducing nucleosome disruption.
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