ACOT7 (NM_007274) Human 3' UTR Clone
CAT#: SC204439
3' UTR clone of acyl-CoA thioesterase 7 (ACOT7) transcript variant hBACHa for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | ACOT7 |
Synonyms | ACH1; ACT; BACH; CTE-II; hBACH; LACH; LACH1 |
ACCN | NM_007274 |
Insert Size | 355 bp |
Sequence Data |
>SC204439 3’UTR clone of NM_007274
The sequence shown below is from the reference sequence of NM_007274. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGACAGGGCCACGCGGAGCCTCAGCCCTAGACTCCCTCCTCCTGCCACTGGTGCCTCGAGTAGCCATGG CAACGGGCCCAGTGTCCAGTCACTTAGAAGTTCCCCCCTTGGCCAAAAACCCAATTCACATTGAGAGCT GGTGTTGTCTGAAGTTTTCGTATCACAGTGTTAACCTGTACTCTCTCCTGCAAACCTACACACCAAAGC TTTATTTATATCATTCCAGTATCAATGCTACACAGTGTTGTCCCGAGCGCCGGGAGGCGTTGGGCAGAA ACCCTCGGGAATGCTTCCGAGCACGCTGTAGGGTATGGGAAGAACCCAGCACCACTAATAAAGCTGCTG CTTGGCTGGA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data | |
RefSeq | NM_007274.4 |
Summary | This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008] |
Locus ID | 11332 |
MW | 13.2 |
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