United States
Germany
Japan
United Kingdom
China
GIRK2 (KCNJ6) (NM_002240) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC210938L2V
- LentiORF®
-
Lenti ORF particles, KCNJ6 (mGFP-tagged) - Human potassium inwardly-rectifying channel, subfamily J, member 6 (KCNJ6), 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 9,975.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | GIRK2 (KCNJ6) (NM_002240) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BIR1; GIRK-2; GIRK2; hiGIRK2; KATP-2; KATP2; KCNJ7; KIR3.2; KPLBS |
| Vector | pLenti-C-mGFP |
| ACCN | NM_002240 |
| ORF Size | 1269 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC210938).
|
| 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_002240.2 |
| RefSeq Size | 2537 bp |
| RefSeq ORF | 1272 bp |
| Locus ID | 3763 |
| Domains | IRK |
| Protein Families | Druggable Genome, Ion Channels: Potassium, Transmembrane |
| MW | 48.5 kDa |
| Gene Summary | This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
