KRT82 Polyclonal Antibody, 20ul Cryogenic Vials Several human genetic disorders are

Several human genetic disorders are caused by aberrations in human homeobox genes

ARVCF contains a predicted nuclear-targeting sequence suggesting that it may have a function as a nuclear protein

YWHAH (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta) product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins

This protein's enzymatic activity prevents the one electron reduction of quinones that results in the production of radical species

Demethylation of Lys residue generates formaldehyde and succinate

KRT82 Polyclonal Antibody, 20ul Cryogenic Vials Several human genetic disorders 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