Cytokeratin 8(CK8) Mouse Monoclonal Antibody

Cytokeratin 8(CK8) Mouse Monoclonal Antibody

Cat: AMM21988
规格:50μL 价格:¥1200
规格:100μL 价格:¥2150
应用(Application):IHC,ELISA

种属(Reactivity):Human,Mouse,Rat
偶联物(Conjugate):Unconjugated
基因名(Gene Name):KRT8 CYK8

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 8(CK8) 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,Mouse,Rat

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Unmodified

同种型(Isotype)

IgG2b,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)

KRT8 CYK8

别名(Alternative Names)

CARD2;CK 8;CK-8;CK8;CYK8;CYKER;Cytokeratin endo A;Cytokeratin-8;DreK8;EndoA;K2C8;K2C8_HUMAN;K8;Keratin 8;Keratin type II cytoskeletal 8;Keratin, type II cytoskeletal 8;Keratin-8;KO;Krt 2.8;KRT8;MGC118110;MGC174782;MGC53564;MGC85764;sb:cb186;Type-II keratin Kb8

基因ID(Gene ID)

Human:3856

蛋白ID(SwissProt ID)

Human:P05787,Mouse:P11679,Rat:Q10758

 

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:54kDa,Observed MW:54kDa

 

研究背景

keratin 8(KRT8) Homo sapiens This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012],

 

研究领域

Pathology


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