Nav1.5 (SCN5A) (NM_000335) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC214689L1V

  • LentiORF®

Lenti ORF particles, SCN5A (Myc-DDK tagged) - Human sodium channel, voltage-gated, type V, alpha subunit (SCN5A), transcript variant 2, 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)
SCN5A mouse monoclonal antibody,clone OTI5E9
    • 100 ul

CNY 1,999.00
CNY 3,600.00


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

Specifications

Product Data
Product Name Nav1.5 (SCN5A) (NM_000335) Human Tagged ORF Clone Lentiviral Particle
Synonyms CDCD2; CMD1E; CMPD2; HB1; HB2; HBBD; HH1; ICCD; IVF; LQT3; Nav1.5; PFHB1; SSS1; VF1
Vector pLenti-C-Myc-DDK
ACCN NM_000335
ORF Size 6045 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC214689).
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_000335.3
RefSeq Size 8526 bp
RefSeq ORF 6048 bp
Locus ID 6331
Protein Families Druggable Genome, Ion Channels: Sodium, Transmembrane
MW 226.6 kDa
Gene Summary The protein encoded by this gene is an integral membrane protein and tetrodotoxin-resistant voltage-gated sodium channel subunit. This protein is found primarily in cardiac muscle and is responsible for the initial upstroke of the action potential in an electrocardiogram. Defects in this gene are a cause of long QT syndrome type 3 (LQT3), an autosomal dominant cardiac disease. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
*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...