United States
Germany
Japan
United Kingdom
China
KCNQ2 (NM_172107) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC212932L1V
- LentiORF®
-
Lenti ORF particles, KCNQ2 (Myc-DDK tagged) - Human potassium voltage-gated channel, KQT-like subfamily, member 2 (KCNQ2), transcript variant 1, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 15,770.00
货期*
详询
规格
| Cited in 1 publication. |
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | KCNQ2 (NM_172107) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BFNC; DEE7; EBN; EBN1; ENB1; HNSPC; KCNA11; KV7.2 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_172107 |
| ORF Size | 2616 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC212932).
|
| 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_172107.2 |
| RefSeq Size | 3251 bp |
| RefSeq ORF | 2619 bp |
| Locus ID | 3785 |
| Protein Families | Druggable Genome, Ion Channels: Potassium, Transmembrane |
| MW | 95.7 kDa |
| Gene Summary | 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 a related protein encoded by the KCNQ3 gene, 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 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Citations (1)
| The use of this cDNA Clones has been cited in the following citations: |
|---|
|
Coexpression and activation of TRPV1 suppress the activity of the KCNQ2/3 channel
,null,
The Journal of General Physiology
,PubMed ID 21844219
[KCNQ2]
|
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
