TRPM6 (NM_017662) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC216965L1V

  • LentiORF®

Lenti ORF particles, TRPM6 (Myc-DDK tagged) - Human transient receptor potential cation channel, subfamily M, member 6 (TRPM6), transcript variant a, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 21,660.00


货期*
详询

规格
    • 200 ul

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

CNY 2,950.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

CNY 5,230.00


Rabbit Polyclonal Anti-TRPM6 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00

Specifications

Product Data
Product Name TRPM6 (NM_017662) Human Tagged ORF Clone Lentiviral Particle
Synonyms CHAK2; HMGX; HOMG; HOMG1; HSH
Vector pLenti-C-Myc-DDK
ACCN NM_017662
ORF Size 5685 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC216965).
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_017662.3
RefSeq Size 8429 bp
RefSeq ORF 6069 bp
Locus ID 140803
Protein Families Druggable Genome, Ion Channels: Transient receptor potential, Protein Kinase, Transmembrane
MW 216.32 kDa
Gene Summary This gene is predominantly expressed in the kidney and colon, and encodes a protein containing an ion channel domain and a protein kinase domain. It is crucial for magnesium homeostasis, and plays an essential role in epithelial magnesium transport and in the active magnesium absorption in the gut and kidney. Mutations in this gene are associated with hypomagnesemia with secondary hypocalcemia. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Apr 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.
Customer Reviews 
Loading...