KCTD7 rabbit pAb

• Background :

  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.[provided by RefSeq, Jan 2011]

• Description :

  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. [provided by RefSeq, Jan 2011],

• Product Name Alternative :

  BTB/POZ domain-containing protein KCTD7

• UniProt :

  Q96MP8

• Swiss Prot :

  Q96MP8

• Reactivity :

  Human; Mouse; Rat

• Immunogen :

  Synthesized peptide derived from human KCTD7. at AA range: 181-230

• Target :

  KCTD7

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA; IHC

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000; IHC-p 1:50-300; ELISA 2000-20000

• Buffer :

  -20°C/1 year

• Molecular Weight :

  33kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  33kD

• Fragment :

  IgG

• Subcellular Location :

  Cell membrane. Cytoplasm, cytosol.

• Other Product Names :

  BTB/POZ domain-containing protein KCTD7

• Gene ID (Human) :

  154881