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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...

We validate the specificity of these antibodies to KCTD7 by testing them on tissues known to express KCTD7 positively and negatively. Browse below to find the KCTD7 antibody that suites your experiment. We have 3 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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KCTD7 Infographic by Boster Bio

KCTD7 protein infographic

All KCTD7 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-KCTD7 Antibody

6 Q&As

Human, Mouse, Rat

WB

$399
Cat # A11066
100μl

KCTD7 (NM_001167961) Human Recombinant Protein

$1062
Cat # PROTQ96MP8
20 µg

KCTD7 (NM_153033) Human Over-expression Lysate

Human

$628
Cat # LS154881
100 µg

KCTD7 Overview

Facts about BTB/POZ domain-containing protein KCTD7.

KCTD7 3D structure

KCTD7 3D structure. Source: alphafold

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

Gene Information

Family

Belongs to:

No superfamily

Family

Alternative Names

BTB/POZ domain-containing protein KCTD7; EPM3FLJ32069; FLJ45891; potassium channel tetramerisation domain containing 7

Molecular Weight

Mass (kDA):
33.132 kDA

Molecular Weight

Genomic Context


Human

Location:	7q11.21
Sequence:	7; NC_000007.14 (66628881..66643229)

Subcellular Localizations

Cell membrane. Cytoplasm, cytosol.

Subcellular Localization

Diseases

Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Myoclonus
Nerve Degeneration
Ataxia
Aortic Valve Insufficiency
Regurgitation
Developmental Delay (disorder)
Dementia
Neuronal Ceroid-lipofuscinoses

Dissection Of Aorta
Blind Vision
Hypertensive Disease
Cardiovascular Diseases
Tonic-clonic Epilepsy
Myoclonus And Ataxia

Disease

Interacting Proteins

DVL3
NIF3L1
TRIM2

Interacting Proteins

Pathways

Response To Drug
Pathogenesis
Localization

Pathways

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
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.