Cytokeratin 13(CK13) Mouse Monoclonal Antibody

Cytokeratin 13(CK13) Mouse Monoclonal Antibody

Cat: AMM21970
规格:50μL 价格:¥1200
规格:100μL 价格:¥2150
应用(Application):IHC,ELISA

种属(Reactivity):Human
偶联物(Conjugate):Unconjugated
基因名(Gene Name):KRT13

分类: 病理IHC抗体 标签: , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

Cytokeratin 13(CK13) Mouse Monoclonal Antibody

描述(Description)

病理IHC抗体

宿主(Host)

Mouse

应用(Application)

IHC,ELISA

种属反应性(Reactivity)

Human

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Unmodified

同种型(Isotype)

IgG1,Kappa

克隆(Clonality)

Monoclonal

形式(Form)

Liquid

存放说明(Storage)

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

储存溶液(Buffer)

PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

纯化方式(Purification)

The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.

 

免疫原

基因名(Gene Name)

KRT13

别名(Alternative Names)

47 kDa cytokeratin;CK-13;CK13;Cytokeratin 13;Cytokeratin-13;K13;K1C13_HUMAN;Ka13;Keratin 13;Keratin;keratin type I cytoskeletal 13;Keratin-13;Krt-1.13;Krt1-13;KRT13;MGC161462;MGC3781;type I cytoskeletal 13;Type I keratin Ka13;WSN2

基因ID(Gene ID)

Human:3860

蛋白ID(SwissProt ID)

Human:P13646,Mouse:P08730,Rat:Q6IFV4

 

产品应用

稀释比(Dilution Ratio)

IHC 1:200-400;ELISA 1:500-5000

蛋白分子量(Molecular Weight)

Calculated MW:50kDa,Observed MW:50kDa

 

研究背景

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],

 

研究领域

Pathology


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