Dystrophia myotonica protein kinase (DMPK) (NM_001081562) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC223643L4V

  • LentiORF®

Lenti ORF particles, DMPK (mGFP-tagged) - Human dystrophia myotonica-protein kinase (DMPK), transcript variant 4, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,132.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol Dystrophia myotonica protein kinase
Synonyms DM; DM1; DM1PK; DMK; MDPK; MT-PK
Mammalian Cell Selection Puromycin
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_001081562
ORF Size 1875 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC223643).
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_001081562.1
RefSeq Size 2873 bp
RefSeq ORF 1878 bp
Locus ID 1760
UniProt ID Q09013
Cytogenetics 19q13.32
Protein Families Druggable Genome, Protein Kinase
MW 69.4 kDa
Gene Summary The protein encoded by this gene is a serine-threonine kinase that is closely related to other kinases that interact with members of the Rho family of small GTPases. Substrates for this enzyme include myogenin, the beta-subunit of the L-type calcium channels, and phospholemman. The 3' untranslated region of this gene contains 5-38 copies of a CTG trinucleotide repeat. Expansion of this unstable motif to 50-5,000 copies causes myotonic dystrophy type I, which increases in severity with increasing repeat element copy number. Repeat expansion is associated with condensation of local chromatin structure that disrupts the expression of genes in this region. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2016]

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