KCTD7 anticorps

N° du produit ABIN7245461

Détail du produit anti-KCTD7 anticorps

Antigène: KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KCTD7 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of human KCTD7

Isotype: IgG

Information d'application

Indications d'application: WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.56 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur KCTD7

Antigène: KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))

Autre désignation: KCTD7 (KCTD7 Produits)

Synonymes: anticorps 4932409E18, anticorps 9430010P06Rik, anticorps zgc:136884, anticorps CLN14, anticorps EPM3, anticorps potassium channel tetramerization domain containing 7, anticorps potassium channel tetramerisation domain containing 7, anticorps KCTD7, anticorps Kctd7, anticorps kctd7

Sujet: 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.

Poids moléculaire:

Observed_MW: Refer to figures

Calculated_MW: 33 kDa

UniProt: Q96MP8