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Read our guarantee »Products:Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> ECM Proteins >> Cytokeratin
Anti-Keratin antibody
See all Keratin products (4) ...
Guinea pig polyclonal to Keratin
ab11217 does not react with mesenchymal, glial, neuronal or muscle cells.
Reacts with
Cow, Human
Keratin isolated from fetal bovine hooves.
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.1% Sodium Azide
Constituents: Whole Serum
Whole antiserum
Affinity purified rabbit sera.
A wide variety of cells contain, in addition to microtubules and microfilaments, another type of fibrous skeletal element which are classified under the category of "intermediate-sized" filaments. These intermediate sized filaments are stable in vivo and show a biochemical heterogeneity which is developmentally regulated. Each class of intermediate filament is restricted in vivo by tissue differentiation; keratins to epithelia, vimentin to mesenchymal cells, desmin to muscle tissues, glial fibrillary acidic protein (GFAP) to astroglia and neurofilament proteins to neurones. Unlike actin and tubulin, where molecular size is highly conserved from cell to cell and species to species, intermediate filament proteins vary greatly in size from class to class as well as species to species.
Polyclonal
IgG
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Microtubules >> Cytokeratin
Signal Transduction >> Cytoskeleton / ECM >> Cytoskeleton >> Intermediate Filaments >> Class I >> Keratin
Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> Structures >> Keratin
Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> ECM Proteins >> Cytokeratin
Our Abpromise guarantee covers the use of ab11217 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IF: 1/20
Constitutively expressed in distinct types of epithelia such as those in oral mucosa, esophagus, papillae of tongue and hair follicle outer root sheath.
Defects in KRT6A are a cause of pachyonychia congenita type 1 (PC1) [MIM:167200]; also known as Jadassohn-Lewandowsky syndrome. PC1 is an autosomal dominant ectodermal dysplasia characterized by hypertrophic nail dystrophy resulting in onchyogryposis (thickening and increase in curvature of the nail), palmoplantar keratoderma, follicular hyperkeratosis, and oral leukokeratosis. Hyperhidrosis of the hands and feet is usually present.
Belongs to the intermediate filament family.
Target information above from: UniProt accessionP02538
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
ab11217 has not yet been referenced specifically in any publications.
Publishing research using ab11217? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
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