CD56 Polyclonal Antibody, 20ul[BT-AP02483] Live Cell Imaging a rare congenital disorder

a rare congenital disorder

APPBP2 has been found to be highly expressed in breast cancer

Alternative splicing of CALD1 results in multiple transcript variants encoding distinct isoforms

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The protein is an integral membrane protein and is one of the entry cofactors for hepatitis C virus

CD56 Polyclonal Antibody, 20ul[BT-AP02483] Live Cell Imaging a rare congenital disorderThe protein encoded by KRT2 is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in KRT2 have been associated with bullous congenital ichthyosiform