TRPM5 (NM_014555) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC210840L4V

  • LentiORF®

Lenti ORF particles, TRPM5 (mGFP-tagged)-Human transient receptor potential cation channel, subfamily M, member 5 (TRPM5), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 21,945.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name TRPM5 (NM_014555) Human Tagged ORF Clone Lentiviral Particle
Synonyms LTRPC5; MTR1
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_014555
ORF Size 3495 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC210840).
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_014555.2
RefSeq Size 3913 bp
RefSeq ORF 3498 bp
Locus ID 29850
Protein Families Druggable Genome, Ion Channels: Transient receptor potential, Transmembrane
Protein Pathways Taste transduction
MW 131.3 kDa
Gene Summary This gene encodes a member of the transient receptor potential (TRP) protein family, which is a diverse group of proteins with structural features typical of ion channels. This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Ca(2+) ions. It is activated by lower concentrations of intracellular Ca(2+), and inhibited by higher concentrations. It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15.5, and has been shown to be imprinted, with exclusive expression from the paternal allele. [provided by RefSeq, Oct 2010]
*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.
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