TRPV6 (NM_018646) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC214982L2V
- LentiORF®
Lenti ORF particles, TRPV6 (mGFP-tagged) - Human transient receptor potential cation channel, subfamily V, member 6 (TRPV6), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | TRPV6 |
Synonyms | ABP/ZF; CAT1; CATL; ECAC2; HRPTTN; HSA277909; LP6728; ZFAB |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_018646 |
ORF Size | 2175 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC214982).
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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_018646.2 |
RefSeq Size | 2918 bp |
RefSeq ORF | 2298 bp |
Locus ID | 55503 |
UniProt ID | Q9H1D0 |
Cytogenetics | 7q34 |
Domains | ANK, ion_trans |
Protein Families | Druggable Genome, Ion Channels: Transient receptor potential, Transmembrane |
MW | 83 kDa |
Gene Summary | This gene encodes a member of a family of multipass membrane proteins that functions as calcium channels. The encoded protein contains N-terminal ankyrin repeats, which are required for channel assembly and regulation. Translation initiation for this protein occurs at a non-AUG start codon that is decoded as methionine. This gene is situated next to a closely related gene for transient receptor potential cation channel subfamily V member 5 (TRPV5). This locus has experienced positive selection in non-African populations, resulting in several non-synonymous codon differences among individuals of different genetic backgrounds. [provided by RefSeq, Feb 2015] |
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