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Home TrueClone ACSL4 Clone

ACSL4 (NM_004458) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC128137 ACSL4 (untagged)-Human acyl-CoA synthetase long-chain family member 4 (ACSL4), transcript variant 1 (10ug) NM_004458.1, 10ug $680 In Stock
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA311299 Goat Anti-FACL4 / ACSL4 Antibody, 100ug $325 3-7 Days
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OriGene Data
Vector:pCMV6-XL6 Insert Size: 4700 Restriction Site:
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence         
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: TransmembraneDruggable Genome
Protein Pathways: Fatty acid metabolismMetabolic pathwaysPPAR signaling pathwayAdipocytokine signaling pathway
Reference Data
RefSeq: NM_004458.1, NP_004449
RefSeq Size: 5039 RefSeq ORF: 2013
Synonyms : ACS4; FACL4; LACS4; MRX63; MRX68
LocusID: 2182 Cytogenetic: Xq22.3 Domains: AMP-binding
Summary: The protein encoded by this gene is an isozyme of the 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 preferentially utilizes arachidonate as substrate. The absence of this enzyme may contribute to the mental retardation or Alport syndrome. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008].

Transcript Variant: This variant (1) encodes the predominant isoform (1) of 670 amino acids.

* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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