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KCTD7 Antibodies
AND KCTD7 ELISA kits, KCTD7 Proteins
Many biological assays use antibodies to detect KCTD7, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with KCTD7 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop KCTD7 antibodies...
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KCTD7 Overview
Facts about BTB/POZ domain-containing protein KCTD7.
BTB/POZ domain-containing protein KCTD7 (KCTD7)
May be involved in the control of excitability of cortical neurons. .
.
Gene Information
| Human | |
|---|---|
| Gene Name: | KCTD7 |
| Uniprot: | Q96MP8 |
| Entrez: | 154881 |
Family
| Belongs to: |
|---|
| No superfamily |
Alternative Names
BTB/POZ domain-containing protein KCTD7; EPM3FLJ32069; FLJ45891; potassium channel tetramerisation domain containing 7
Molecular Weight
Mass (kDA):
33.132 kDA
Genomic Context
| Human | |
|---|---|
| Location: | 7q11.21 |
| Sequence: | 7; NC_000007.14 (66628881..66643229) |
Subcellular Localizations
Cell membrane. Cytoplasm, cytosol.
Diseases
- Epilepsy
- Epilepsies, Myoclonic
- Myoclonic Epilepsies, Progressive
- Myoclonus
- Nerve Degeneration
- Ataxia
- Aortic Valve Insufficiency
- Regurgitation
- Developmental Delay (disorder)
- Dementia
- Neuronal Ceroid-lipofuscinoses
Interacting Proteins
- DVL3
- NIF3L1
- TRIM2
Pathways
- Response To Drug
- Pathogenesis
- Localization
For details, visit:
bosterbio.com/bosterbio-gene-info-cards/KCTD7
bosterbio.com/bosterbio-gene-info-cards/KCTD7
References
PMID: 17455289 by Van Bogaert P., et al. Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.
PMID: 22748208 by Staropoli J.F., et al. A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.