ENPP1 (NM_006208) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209222L2V
- LentiORF®
-
Lenti ORF particles, ENPP1 (mGFP-tagged) - Human ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), 200ul, >10^7 TU/mL
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CNY 9,975.00
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规格
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经常一起买 (3)
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-mGFP |
ACCN | NM_006208 |
ORF Size | 2619 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209222).
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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_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] |
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