KCTD7 Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-18176
宿主: Rabbit
反应性: H,M,R
应用: WB,IHC
Overview
Synonyms | BTB/POZ domain containing protein KCTD7,EPM3,FLJ32069,Potassium channel tetramerisation domain containing 7,KCTD7抗体 |
Swissprot | Q96MP8 |
Source | Rabbit |
Reactivity | Human,Mouse,Rat |
Immunogen | Synthetic peptide of human KCTD7 |
Application | WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213) |
Recommended dilution | WB,,1:1000-1:5000;IHC,,1:50-1:300; |
Concentration | 1.56mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Cytosol,Plasma Membrane,Other locations:cytoplasm |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
Background | 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. |
Images
Western blot analysis of Hela cell lysate using KCTD7 Polyclonal Antibody at dilution of 1:1200
Immunohistochemistry of paraffin-embedded Human brain tissue using KCTD7 Polyclonal Antibody at dilution of 1:55(×200)
Immunohistochemistry of paraffin-embedded Human liver cancer tissue using KCTD7 Polyclonal Antibody at dilution of 1:55(×200)