KCTD7 Antibody

Code CSB-PA850395LA01HU
Size US$166
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Image
  • Immunofluorescence staining of A549 cells with CSB-PA850395LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) KCTD7 Polyclonal antibody
Uniprot No.
Target Names
KCTD7
Alternative Names
KCTD7 antibody; BTB/POZ domain-containing protein KCTD7 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human BTB/POZ domain-containing protein KCTD7 protein (5-152AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The KCTD7 Antibody (Product code: CSB-PA850395LA01HU) is Non-conjugated. For KCTD7 Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA850395LB01HU KCTD7 Antibody, HRP conjugated ELISA
FITC CSB-PA850395LC01HU KCTD7 Antibody, FITC conjugated
Biotin CSB-PA850395LD01HU KCTD7 Antibody, Biotin conjugated ELISA
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, IF
Recommended Dilution
Application Recommended Dilution
IF 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
May be involved in the control of excitability of cortical neurons.
Gene References into Functions
  1. KCTD7 has an impact on K+ fluxes, neurotransmitter synthesis and neuronal function, and that malfunction of the encoded protein may lead to progressive myoclonus epilepsy. PMID: 27742667
  2. reviews the phenotype of progressive myoclonic epilepsy associated with KCTD7 mutations [review] PMID: 27629772
  3. This study identified that novel KCTD7 mutation in patients with progressive myoclonus epilepsy with ataxia. PMID: 25060828
  4. The KCTD7 gene, previously associated with progressive myoclonus epilepsies (PMEs) in a single inbred family, was screened for mutations in 18 Turkish PME patients. PMID: 22693283
  5. this study clearly demonstrates that KCTD7 mutations also cause a rare, infantile-onset NCL subtype designated as CLN14. PMID: 22748208
  6. We found a C to T mutation in exon 2 of the potassium channel tetramerization domain containing 7 gene(KCTD7)in a progressive myoclonic epilepsy family affecting a highly conserved segment of the predicted protein changing an arginine codon to a stop. PMID: 17455289

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Involvement in disease
Epilepsy, progressive myoclonic 3, with or without intracellular inclusions (EPM3)
Subcellular Location
Cell membrane. Cytoplasm, cytosol.
Database Links

HGNC: 21957

OMIM: 611725

KEGG: hsa:154881

UniGene: Hs.546627

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