ACSL6 (NM_001205251) Human Untagged Clone

CAT#: SC331645

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


  "NM_001205251" in other vectors (2)

Reconstitution Protocol

USD 640.00

5 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol ACSL6
Synonyms ACS2; FACL6; LACS2; LACS5; LACS 6
Vector pCMV6 series
Sequence Data
>NCBI ORF sequence for NM_001205251, the custom clone sequence may differ by one or more nucleotides


ATGCAGACACAGGAGATCCTGAGGATACTGCGACTGCCTGAGCTAGGTGACTTGGGACAGTTTTTCCGCA
GCCTCTCGGCCACCACCCTCGACAGTGGCGGGGCACGGCGATCTGTGATTGGGTCTGGCCCTCAGCTACT
TACCCACTACTATGATGATGCCCGGACCATGTACCAGGTGTTCCGCCGTGGGCTTAGCATCTCAGGGAAT
GGGCCCTGTCTTGGTTTCAGGAAGCCTAAGCAGCCTTACCAGTGGCTGTCCTACCAGGAGGTGGCCGACA
GGGCTGAATTTCTGGGGTCCGGACTTCTCCAGCACAATTGTAAAGCATGCACTGATCAGTTTATTGGTGT
TTTTGCACAAAATCGGCCAGAGTGGATCATTGTGGAGCTGGCCTGCTACACATATTCCATGGTGGTGGTC
CCGCTCTATGACACCCTGGGCCCTGGGGCTATCCGCTACATCATCAATACAGCGGACATCAGCACCGTGA
TTGTGGACAAACCTCAGAAGGCTGTGCTTCTGCTAGAGCATGTGGAGAGGAAGGAGACTCCAGGCCTCAA
GCTGATCATCCTCATGGACCCATTCGAAGAAGCCCTGAAAGAGAGAGGGCAGAAGTGCGGGGTGGTCATT
AAGTCCATGCAGGCCGTGGAGGACTGTGGCCAAGAGAATCACCAGGCTCCTGTGCCCCCGCAGCCTGATG
ACCTCTCCATTGTGTGTTTCACAAGCGGCACGACAGGGAACCCAAAAGGTGCGATGCTCACCCATGGGAA
CGTGGTGGCTGATTTCTCAGGCTTTCTGAAAGTGACAGAGGGAGATATCCGCCTTCTCTCAGATGACATG
AAGGCTCTATGCCCCACCATCTTCCCTGTGGTCCCACGACTGCTGAACCGGATGTACGACAAGATCTTCA
GCCAGGCAAACACACCATTAAAGCGCTGGCTCCTGGAGTTTGCAGCAAAGCGTAAGCAAGCCGAGGTCCG
GAGTGGAATCATCAGGAATGATAGTATCTGGGATGAACTCTTCTTTAATAAGATTCAGGCCAGTCTTGGT
GGGTGTGTGCGGATGATTGTTACTGGAGCAGCCCCAGCATCACCAACAGTTCTGGGATTTCTCCGGGCAG
CTCTAGGGTGCCAGGTTTATGAAGGTTATGGCCAAACTGAGTGCACAGCTGGATGTACCTTCACCACTCC
TGGCGACTGGACCTCAGGGCACGTAGGGGCGCCACTTCCCTGCAATCATATCAAGCTCGTTGATGTTGAG
GAACTGAACTACTGGGCCTGCAAAGGAGAGGGAGAGATATGTGTGAGAGGACCAAATGTGTTCAAAGGCT
ACTTGAAAGATCCAGACAGGACGAAGGAGGCCCTGGACAGCGATGGCTGGCTTCACACTGGAGACATCGG
AAAATGGCTGCCGGCAGGAACTCTTAAAATTATTGATCGGAAAAAGCATATATTTAAACTTGCTCAGGGA
GAATATGTTGCACCCGAGAAGATTGAGAACATCTACATCCGGAGCCAACCTGTGGCGCAAATCTATGTCC
ATGGGGACAGCTTAAAGGCCTTTTTGGTAGGCATTGTTGTGCCTGACCCTGAAGTTATGCCCTCCTGGGC
CCAGAAGAGAGGAATTGAAGGAACATATGCAGATCTCTGCACAAATAAGGATCTGAAGAAAGCCATTTTG
GAAGATATGGTGAGGTTAGGAAAAGAAAGTGGACTCCATTCTTTTGAGCAGGTTAAAGCCATTCACATCC
ATTCTGACATGTTCTCAGTTCAAAATGGCTTGCTGACACCAACACTAAAAGCTAAGAGACCTGAGCTGAG
AGAGTACTTCAAAAAACAAATAGAAGAGCTTTACTCAATCTCCATGTGA


Restriction Sites SgfI-MluI     
ACCN NM_001205251
ORF Size 1869 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_001205251.1, NP_001192180.1
RefSeq Size 6316
RefSeq ORF 1869
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 (6) differs in the 5' UTR and coding sequence and lacks two alternate in-frame coding sequences compared to variant 1. The resulting isoform (f) is shorter at the N-terminus and lacks two internal segments 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.

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