TRPM5 (NM_014555) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC210840L2V
- LentiORF®
Lenti ORF particles, TRPM5 (mGFP-tagged)-Human transient receptor potential cation channel, subfamily M, member 5 (TRPM5), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | TRPM5 |
Synonyms | LTRPC5; MTR1 |
Vector | pLenti-C-mGFP |
ACCN | NM_014555 |
ORF Size | 3495 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC210840).
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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, NP_055370.1 |
RefSeq Size | 3913 |
RefSeq ORF | 3498 |
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] |
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