KCTD7 Polyclonal Antibody, 50ul Protein Modification with deletion of the Golgi

with deletion of the Golgi and endoplasmic reticulum signals resulting in abnormal subcellular localization

reproductive function

This protein contains conserved DLG (asp-leu-gly) and ENIL (glu-asn-ile-leu) motifs

and p53-mediated effects on growth

KCTD7 Polyclonal Antibody, 50ul Protein Modification with deletion of the GolgiThis gene encodes a member of the potassium channel tetramerization domain containing protein family. Family members are identified on a structural basis and contain an amino terminal domain similar to the T1 domain present in the voltage gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy 3. Alternative splicing results in multiple transcript variants.