Cytokeratin 13 Rabbit Monoclonal Antibody

Cytokeratin 13 Rabbit Monoclonal Antibody

Cat: AMRe86647
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,FC
Reaktivite:Human,Mouse
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Cytokeratin 13
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,
Cytokeratin 13 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,FC
Reaktivite
Human,Mouse
Gen Adı
Cytokeratin 13
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Cytokeratin 13 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 Cytokeratin 13
Alternatif İsimler K13; CK13; WSN2
Gen Kimliği 3860
SwissProt Kimliği P13646
İmmünojen A synthetic peptide of human Cytokeratin 13
Uygulama
Uygulama WB,IHC,ICC/IF,FC
Seyreltme Oranı WB 1:5000-1:50000,IHC 1:100-1:200,ICC/IF 1:200-1:500,FC 1:20-1:50
Moleküler Ağırlık Calculated MW:50 kDa; Observed MW:50 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008]
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