human KCNQ3 Over-expression AAV
Category: AAV > Over-Expression
Cat. No: AAV-212773
Availability:
3-5 weeks
Name:
AAV-h-KCNQ3
This is an AAV expressing Human KCNQ3.
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Viral Details
- Viral Backbone
- Recombinant AAV
- AAV-ITR
- AAV2
- AAV Serotype
- Available in AAV1, AAV2, AAV3, AAV5, AAV6, AAV8, AAV9, AAV-DJ, AAV-DJ8, AAV-DJ9 and other wildtype/synthetic AAV capsids
- Promoter
- CMV (default), or choose from 30 different ubiquitous or cell specific promoter
- Reporter
- none, optional GFP, CFP, YFP, RFP or mCherry
- Storage Buffer
- PBS/5% Glycerol
Gene Details
- Species
- Human
- Gene Symbol
- KCNQ3
- Gene Name
- potassium voltage-gated channel subfamily Q member 3
- Gene ID
- 3786
- Gene Synonyms
- BFNC2; EBN2; KV7.3
- ORF Size
- 2616 bp
- RefSeq#
- BC152755
- Gene Description
- The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Two variants encoding distinct isoforms have been found.
- UniGene ID
- Hs.374023
- HGNC ID
- HGNC:6297
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