KRT5 (Human) IP-WB Antibody Pair
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More Files
- More Functions
Immunoprecipitation of KRT5 transfected lysate using mouse monoclonal anti-KRT5 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-KRT5.
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Specification
Product Description
This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.
Reactivity
Human
Quality Control Testing
Immunoprecipitation-Western Blot (IP-WB)
Immunoprecipitation of KRT5 transfected lysate using mouse monoclonal anti-KRT5 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-KRT5.
Supplied Product
Antibody pair set content:
1. Antibody pair for IP: mouse monoclonal anti-KRT5 (300 ug)
2. Antibody pair for WB: rabbit polyclonal anti-KRT5 (50 ul)
Storage Instruction
Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
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Applications
Immunoprecipitation-Western Blot
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Gene Info — KRT5
Entrez GeneID
3852Gene Name
KRT5
Gene Alias
CK5, DDD, EBS2, K5, KRT5A
Gene Description
keratin 5
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene is a member of the keratin gene family. 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. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq
Other Designations
58 kda cytokeratin|epidermolysis bullosa simplex 2 Dowling-Meara/Kobner/Weber-Cockayne types|keratin 5 (epidermolysis bullosa simplex, Dowling-Meara/Kobner/Weber-Cockayne types)|keratin, type II cytoskeletal 5
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Interactome
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Disease
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