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KCNC1 (NM_004976) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC215716L1V
- LentiORF®
-
Lenti ORF particles, KCNC1 (Myc-DDK tagged) - Human potassium voltage-gated channel, Shaw-related subfamily, member 1 (KCNC1), transcript variant B, 200ul, >10^7 TU/mL
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CNY 9,690.00
货期*
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规格
| Cited in 2 publications. |
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经常一起买 (3)
Specifications
| Product Data | |
| Product Name | KCNC1 (NM_004976) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | EPM7; KV3.1; KV4; NGK2 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_004976 |
| ORF Size | 1533 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC215716).
|
| 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_004976.2 |
| RefSeq Size | 1602 bp |
| RefSeq ORF | 1536 bp |
| Locus ID | 3746 |
| Protein Families | Druggable Genome, Ion Channels: Potassium, Transmembrane |
| MW | 57.8 kDa |
| Gene Summary | This gene encodes a member of a family of integral membrane proteins that mediate the voltage-dependent potassium ion permeability of excitable membranes. Alternative splicing is thought to result in two transcript variants encoding isoforms that differ at their C-termini. These isoforms have had conflicting names in the literature: the longer isoform has been called both "b" and "alpha", while the shorter isoform has been called both "a" and "beta" (PMIDs 1432046, 12091563). [provided by RefSeq, Oct 2014] |
Citations (2)
| The use of this cDNA Clones has been cited in the following citations: |
|---|
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KCNC1‐related disorders: new de novo variants expand the phenotypic spectrum, et al. KCNC1‐related disorders: new de novo variants expand the phenotypic spectrum
,null,
Annals of Clinical and Translational Neurology
,PubMed ID 31353862
[KCNC1]
|
|
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.
,null,
Annals of neurology
,PubMed ID 28380698
[KCNC1]
|
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