GIRK2 (KCNJ6) (NM_002240) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC210938L1V

  • LentiORF®

Lenti ORF particles, KCNJ6 (Myc-DDK tagged) - Human potassium inwardly-rectifying channel, subfamily J, member 6 (KCNJ6), 200ul, >10^7 TU/mL

Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 820.00

3 Weeks*

Size
    • 200 ul

Product Images

Other products for "KCNJ6"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol KCNJ6
Synonyms BIR1; GIRK-2; GIRK2; hiGIRK2; KATP-2; KATP2; KCNJ7; KIR3.2; KPLBS
Vector pLenti-C-Myc-DDK
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, NP_002231.1
RefSeq Size 2537 bp
RefSeq ORF 1272 bp
Locus ID 3763
Cytogenetics 21q22.13
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]'

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.