KRT13 monoclonal antibody, clone 3G4
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More Files
- More Functions
Western Blot (Cell lysate)
Western blot analysis of T47D cell with KRT13 monoclonal antibody.
Enzyme-linked Immunoabsorbent Assay
ELISA analysis of KRT13 monoclonal antibody, clone 3G4.
Flow Cytometry
Flow cytometric analysis of HeLa cells with KRT13 monoclonal antibody (green) and negative control (red).
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Specification
Product Description
Mouse monoclonal antibody raised against recombinant human KRT13.
Immunogen
Recombinant protein corresponding to amino acids 143-295 of human KRT13 from E. coli.
Host
Mouse
Theoretical MW (kDa)
52
Reactivity
Human
Form
Liquid
Isotype
IgG1
Recommend Usage
ELISA (1:10000)
Flow Cytometry (1:200-1:400)
Immunocytochemistry
Immunohistochemistry
Western Blot (1:500-1:2000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.05% sodium azide).
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of T47D cell with KRT13 monoclonal antibody.Enzyme-linked Immunoabsorbent Assay
ELISA analysis of KRT13 monoclonal antibody, clone 3G4.Flow Cytometry
Flow cytometric analysis of HeLa cells with KRT13 monoclonal antibody (green) and negative control (red). -
Gene Info — KRT13
Entrez GeneID
3860Gene Name
KRT13
Gene Alias
CK13, K13, MGC161462, MGC3781
Gene Description
keratin 13
Gene Ontology
HyperlinkGene Summary
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
Other Designations
cytokeratin 13|keratin, type I cytoskeletal 13
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