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KCNE3 (NM_005472) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC210303L4V
- LentiORF®
-
Lenti ORF particles, KCNE3 (mGFP-tagged) - Human potassium voltage-gated channel, Isk-related family, member 3 (KCNE3), 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
| Product Data | |
| Product Name | KCNE3 (NM_005472) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BRGDA6; HOKPP; HYPP; MiRP2 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_005472 |
| ORF Size | 309 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC210303).
|
| 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_005472.3 |
| RefSeq Size | 3070 bp |
| RefSeq ORF | 312 bp |
| Locus ID | 10008 |
| Protein Families | Druggable Genome, Ion Channels: Other, Transmembrane |
| MW | 11.7 kDa |
| Gene Summary | Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the kidney. A missense mutation in this gene is associated with hypokalemic periodic paralysis. [provided by RefSeq, Jul 2008] |
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