Technical Data
Cytokeratin 10 (Keratin, Type I Cytoskeletal 10, Cytokeratin-10, CK-10, Keratin-10, K10, KRT10, KPP)
Among the cytoplasmic intermediate filaments (IF) proteins, keratins make up the largest family and are expressed specifically in epithelial cells in a cell-specific manner. Keratins include more than 20 unique gene products (termed K1-K20) that are divided into type I (K9-K20) and type II (K1-K8). Most epithelial cells express at least one type I and one type II keratin as their predominant IF protein complement in an epithelial cell-specific manner. Cytokeratin 10 is a member of the type I (acidic) cytokeratin family. Cytokeratin 10 is synthesized in the suprabasal cell layers of certain stratified epithelia, in an endogenous differentiation program and is expressed in certain epithelial tumors and is generally associated with keratin-1. Its deficiency leads to epidermolytic hyperkeratosis (EHK). The type I cytokeratins are clustered in a region of chromosome 17q21.2.

Suitable for use in Immunohistochemistry. Other applications not tested.

Recommended Dilution:
Immunohistochemistry (formalin fixed paraffin embedded): 1:25-1:50
Immunohistochemistry: Frozen
Optimal dilutions to be determined by the researcher.

Positive Control:

Storage and Stability:
May be stored at 4C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
500ul-20CBlue IceHumanMouse
Not determined
Crude cytoskeletal extract prepared from the epidermal component of trypsin-split normal adult skin. Cellular Localization: Cytoplasmic.
Supplied as a liquid, 0.05% sodium azide.
Recognizes human Cytokeratin 10. Species Crossreactivity: porcine and rat.
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.
1. Ivanyi et al. J Pathol 159: 7, 1989. 2. Ivanyi et al. Can Res 50: 5143, 1990. 3. Leigh et al. British J Dermatol 129: 110, 1993. 4. Muller et al. Hum Mol Genet 15: 1133, 2006.