SHOX2 Rabbit Polyclonal Antibody, 100ul Cell Proliferation Mutations in the gene encoding

Mutations in the gene encoding CABC1 may be implicated in ubiquinone deficiency which can lead to cerebellar ataxia and seizures

Rab GTPases are active

a family of serine/threonine p21-activating kinases

Three transcript variants encoding the same protein have been found for NFIL3

this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter

SHOX2 Rabbit Polyclonal Antibody, 100ul Cell Proliferation Mutations in the gene encodingThis gene is a member of the homeobox family of genes that encode proteins containing a 60 amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is