ACSL6 (NM_001205250) Human Untagged Clone

CAT#: SC331644

ACSL6 (untagged) - Homo sapiens acyl-CoA synthetase long-chain family member 6 (ACSL6), transcript variant 5

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ACSL6
• Synonyms: ACS2; FACL6; LACS2; LACS5; LACS 6
• Vector: pCMV6 series
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001205250, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCCAGAGTTTGTCCTCTCACTTCTGGAGAAGATGCAGACACAGGAGATCCTGAGGATACTGCGACTGC
  CTGAGCTAGGTGACTTGGGACAGTTTTTCCGCAGCCTCTCGGCCACCACCCTCGTGAGTATGGGTGCCCT
  GGCTGCCATCCTTGCCTACTGGTTCACTCACCGGCCAAAGGCCTTGCAGCCGCCATGCAACCTCCTGATG
  CAGTCAGAAGAAGTAGAGGACAGTGGCGGGGCACGGCGATCTGTGATTGGGTCTGGCCCTCAGCTACTTA
  CCCACTACTATGATGATGCCCGGACCATGTACCAGGTGTTCCGCCGTGGGCTTAGCATCTCAGGGAATGG
  GCCCTGTCTTGGTTTCAGGAAGCCTAAGCAGCCTTACCAGTGGCTGTCCTACCAGGAGGTGGCCGACAGG
  GCTGAATTTCTGGGGTCCGGACTTCTCCAGCACAATTGTAAAGCATGCACTGATCAGTTTATTGGTGTTT
  TTGCACAAAATCGGCCAGAGTGGATCATTGTGGAGCTGGCCTGCTACACATATTCCATGGTGGTGGTCCC
  GCTCTATGACACCCTGGGCCCTGGGGCTATCCGCTACATCATCAATACAGCGGACATCAGCACCGTGATT
  GTGGACAAACCTCAGAAGGCTGTGCTTCTGCTAGAGCATGTGGAGAGGAAGGAGACTCCAGGCCTCAAGC
  TGATCATCCTCATGGACCCATTCGAAGAAGCCCTGAAAGAGAGAGGGCAGAAGTGCGGGGTGGTCATTAA
  GTCCATGCAGGCCGTGGAGGACTGTGGCCAAGAGAATCACCAGGCTCCTGTGCCCCCGCAGCCTGATGAC
  CTCTCCATTGTGTGTTTCACAAGCGGCACGACAGGGAACCCAAAAGGTGCGATGCTCACCCATGGGAACG
  TGGTGGCTGATTTCTCAGGCTTTCTGAAAGTGACAGAGAAAGTGATCTTTCCGAGACAGGACGATGTGCT
  CATCTCCTTCCTGCCTCTGGCTCACATGTTTGAGAGAGTAATCCAGTCTGTCGTCTATTGCCACGGAGGG
  CGTGTTGGCTTCTTCCAGGGAGATATCCGCCTTCTCTCAGATGACATGAAGGCTCTATGCCCCACCATCT
  TCCCTGTGGTCCCACGACTGCTGAACCGGATGTACGACAAGATCTTCAGCCAGGCAAACACACCATTAAA
  GCGCTGGCTCCTGGAGTTTGCAGCAAAGCGTAAGCAAGCCGAGGTCCGGAGTGGAATCATCAGGAATGAT
  AGTATCTGGGATGAACTCTTCTTTAATAAGATTCAGGCCAGTCTTGGTGGGTGTGTGCGGATGATTGTTA
  CTGGAGCAGCCCCAGCATCACCAACAGTTCTGGGATTTCTCCGGGCAGCTCTAGGGTGCCAGGTTTATGA
  AGGTTATGGCCAAACTGAGTGCACAGCTGGATGTACCTTCACCACTCCTGGCGACTGGACCTCAGGGCAC
  GTAGGGGCGCCACTTCCCTGCAATCATATCAAGCTCGTTGATGTTGAGGAACTGAACTACTGGGCCTGCA
  AAGGAGAGGGAGAGATATGTGTGAGAGGACCAAATGTGTTCAAAGGCTACTTGAAAGATCCAGACAGGAC
  GAAGGAGGCCCTGGACAGCGATGGCTGGCTTCACACTGGAGACATCGGAAAATGGCTGCCGGCAGGAACT
  CTTAAAATTATTGATCGGAAAAAGCATATATTTAAACTTGCTCAGGGAGAATATGTTGCACCCGAGAAGA
  TTGAGAACATCTACATCCGGAGCCAACCTGTGGCGCAAATCTATGTCCATGGGGACAGCTTAAAGGCCTT
  TTTGGTAGGCATTGTTGTGCCTGACCCTGAAGTTATGCCCTCCTGGGCCCAGAAGAGAGGAATTGAAGGA
  ACATATGCAGATCTCTGCACAAATAAGGATCTGAAGAAAGCCATTTTGGAAGATATGGTGAGGTTAGGAA
  AAGAAAGTGGACTCCATTCTTTTGAGCAGGTTAAAGCCATTCACATCCATTCTGACATGTTCTCAGTTCA
  AAATGGCTTGCTGACACCAACACTAAAAGCTAAGAGACCTGAGCTGAGAGAGTACTTCAAAAAACAAATA
  GAAGAGCTTTACTCAATCTCCATGTGA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001205250
• ORF Size: 2127 bp
• 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).

Reference Data

• RefSeq: NM_001205250.1, NP_001192179.1
• RefSeq Size: 6551
• RefSeq ORF: 2127
• Locus ID: 23305
• Protein Families: Druggable Genome, Transmembrane
• Protein Pathways: Adipocytokine signaling pathway, Fatty acid metabolism, Metabolic pathways, PPAR signaling pathway
• Gene Summary: The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2011]
  Transcript Variant: This variant (5) differs in the 5' UTR and coding sequence compared to variant 1. The resulting isoform (e) is shorter at the N-terminus compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.