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Precision Science Group
(PSG)
CK8 Mouse Antibody
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene.
Alternative Name(s)
KRT8
Application
WB
UNIprot
p05787
clonality
Monoclonal
reactivity
Human
Research area
Others
source
Mouse
storage
Store at -20℃, stable for one year from the date of shipment.
CK8 Mouse Antibody
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