FATP2 (SLC27A2) (NM_003645) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC221033L3V

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  • LentiORF®

Lenti ORF particles, SLC27A2 (Myc-DDK tagged) - Human solute carrier family 27 (fatty acid transporter), member 2 (SLC27A2), transcript variant 1, 200ul, >10^7 TU/mL



USD 1,127.00

5 Weeks*

Size
    • 200 ul

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol SLC27A2
Synonyms ACSVL1; FACVL1; FATP2; hFACVL1; HsT17226; VLACS; VLCS
Mammalian Cell Selection Puromycin
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_003645
ORF Size 1860 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC221033).
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_003645.2
RefSeq Size 2343 bp
RefSeq ORF 1863 bp
Locus ID 11001
UniProt ID O14975
Cytogenetics 15q21.2
Domains AMP-binding
Protein Families Transmembrane
Protein Pathways PPAR signaling pathway
MW 70.1 kDa
Gene Summary The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]
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*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.