KCNQ3 (NM_004519) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC218739L3V
- LentiORF®
Lenti ORF particles, KCNQ3 (Myc-DDK tagged) - Human potassium voltage-gated channel, KQT-like subfamily, member 3 (KCNQ3), transcript variant 1, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK mGFP mGFP w/ Puro
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | KCNQ3 |
Synonyms | BFNC2; EBN2; KV7.3 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_004519 |
ORF Size | 2616 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC218739).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_004519.2 |
RefSeq Size | 3097 bp |
RefSeq ORF | 2619 bp |
Locus ID | 3786 |
UniProt ID | O43525 |
Cytogenetics | 8q24.22 |
Protein Families | Druggable Genome, Ion Channels: Potassium, Transmembrane |
MW | 96.6 kDa |
Gene Summary | This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are 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). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014] |
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