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  • Accession
  • Catalog #

Cytokeratin 5 AntibodyMouse Monoclonal Antibody to Cytokeratin 5

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AO1256a 0.1ml 400 ul 7-10 days $ 325.00 Add to cart
  • Specification
  • Citiations : 0
  • Reviews
  • Protocols
  • Backgrounds

Cytokeratin 5 Antibody - Product info

ApplicationWB
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionP13647
Other AccessionNP_000415.2
ReactivityHuman
IsotypeMouse IgG1
Clone Names10
Calculated MW62378 Da

Cytokeratin 5 Antibody - Additional info

Gene ID 3852
Other Names
K5; CK5; KRT5A; KRT5
Target/Specificity
Purified recombinant fragment of Cytokeratin 5 expressed in E. Coli.
Dilution
WB~~1:500 - 2000.
Format
Purified recombinant fragment of Cytokeratin 5 expressed in E. Coli.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
Cytokeratin 5 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.

Cytokeratin 5 Antibody - Protein Information

Name KRT5

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Provided below are standard protocols that you may find useful for product applications.

BACKGROUND

Cytokeratin 5, also known as CK5, KRT5. It is a member of the keratin gene family. Biochemically, most members of the CK family fall into one of two classes, type I (acidic polypeptides) and type II (basic polypeptides). The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. At least one member of the acidic family and one member of the basic family is expressed in all epithelial cells. Cytokeratin 5 is expressed in normal basal cells. Mutations of the Cytokeratin5 gene (KRT5) have been shown to result in the autosomal dominant disorderepidermolysis bullosa (EB). Defects in KRT5 are a cause of epidermolysis bullosa simplex.

REFERENCES

1. J Invest Dermatol. 2003 Sep;121(3):482-5.
2. J Cell Sci. 2005 Mar 1;118(Pt 5):1081-90.