ENPP1 (NM_006208) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC209222L3V

  • LentiORF®

Lenti ORF particles, ENPP1 (Myc-DDK tagged) - Human ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,930.00


货期*
详询

规格
    • 200 ul

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Specifications

Product Data
Product Name ENPP1 (NM_006208) Human Tagged ORF Clone Lentiviral Particle
Synonyms ARHR2; COLED; M6S1; NPP1; NPPS; PC-1; PCA1; PDNP1
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_006208
ORF Size 2619 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC209222).
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_006208.1, NP_006199.1
RefSeq Size 7442 bp
RefSeq ORF 2778 bp
Locus ID 5167
Domains SO, Endonuclease, Phosphodiest
Protein Families Druggable Genome, Transmembrane
Protein Pathways Metabolic pathways, Nicotinate and nicotinamide metabolism, Pantothenate and CoA biosynthesis, Purine metabolism, Riboflavin metabolism, Starch and sucrose metabolism
MW 99.9 kDa
Gene Summary This gene is a member of the ecto-nucleotide pyrophosphatase/phosphodiesterase (ENPP) family. The encoded protein is a type II transmembrane glycoprotein comprising two identical disulfide-bonded subunits. This protein has broad specificity and cleaves a variety of substrates, including phosphodiester bonds of nucleotides and nucleotide sugars and pyrophosphate bonds of nucleotides and nucleotide sugars. This protein may function to hydrolyze nucleoside 5' triphosphates to their corresponding monophosphates and may also hydrolyze diadenosine polyphosphates. Mutations in this gene have been associated with 'idiopathic' infantile arterial calcification, ossification of the posterior longitudinal ligament of the spine (OPLL), and insulin resistance. [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.
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