K1107抗体应用：WB 1:500-2000

K121L抗体应用：WB 1:500-2000

K1257抗体应用：WB 1:500-2000

K1456抗体应用：WB 1:500-2000

K1614抗体应用：WB 1:500-2000

K1737抗体应用：WB 1:500-2000

K1751抗体应用：WB 1:500-2000

K1C12抗体应用：WB 1:500-2000 ELISA 1:5000-20000keratin 12(KRT12) Homo sapiens KRT12 encodes the type I intermediate filament chain keratin 12, expressed in corneal epithelia. Mutations in this gene lead to Meesmann corneal dystrophy. [provided by RefSeq, Jul 2008],

K1C23抗体应用：WB 1:500-2000 ELISA 1:5000-20000keratin 23(KRT23) Homo sapiens The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013],

K1C9抗体应用：WB 1:500-2000 ELISA 1:5000-20000keratin 9(KRT9) Homo sapiens This gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma. [provided by RefSeq, Jul 2008],