KCTD7 Polyclonal Antibody

KCTD7

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Refer to figures

KCTD7 (Potassium Channel Tetramerization Domain Containing 7) is a Protein Coding gene. Diseases associated with KCTD7 include Epilepsy, Progressive Myoclonic 3, With Or Without Intracellular Inclusions and Cln14 Disease. Among its related pathways are Neuropathic Pain-Signaling in Dorsal Horn Neurons and Innate Immune System. An important paralog of this gene is KCTD14. This 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.

PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

WB 1:500-1:2000

Polyclonal

Polyclonal Antibodies