KRT82 Polyclonal Antibody, 50ul Fluorescent Staining Mutations in this gene are

Mutations in this gene are associated with osteogenesis imperfecta types I-IV

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membrane bound isoforms

This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment

or skeletal muscle

KRT82 Polyclonal Antibody, 50ul Fluorescent Staining Mutations in this gene areThe protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less related subfamily includes