FAR2 (NM_001271783) Human Untagged Clone
CAT#: SC333109
FAR2 (untagged) - Homo sapiens fatty acyl CoA reductase 2 (FAR2), transcript variant 1
CNY 4940.00
货期*
5周
规格
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Synonyms | HEL-S-81; MLSTD1; SDR10E2 |
Vector | pCMV6-Entry |
Sequence Data |
>SC333109 representing NM_001271783.
Blue=Insert sequence Red=Cloning site Green=Tag(s) ATGTCCACAATTGCAGCTTTCTATGGCGGCAAGTCCATTCTCATCACGGGGGCCACAGGCTTTCTGGGC AAAGTGCTGATGGAGAAGCTGTTTCGCACCAGCCCAGACCTGAAAGTCATTTACATCCTTGTGAGGCCC AAGGCTGGCCAGACACTGCAGCAGAGGGTTTTCCAGATCCTAGACAGTAAGCTATTTGAGAAAGTCAAA GAAGTTTGTCCAAATGTGCATGAGAAGATCAGAGCTATTTATGCAGATCTCAATCAGAATGACTTTGCC ATCAGCAAAGAGGACATGCAGGAGCTTCTCTCCTGTACAAACATAATATTTCACTGTGCAGCCACTGTA CGCTTTGACGACACTCTCAGACATGCTGTGCAACTTAACGTCACTGCCACCCGGCAGCTCTTGCTTATG GCTAGTCAGATGCCAAAGCTGGAAGCCTTTATACATATCTCTACTGCCTATTCAAATTGTAACCTGAAG CACATCGATGAAGTTATCTATCCGTGCCCTGTGGAGCCAAAAAAAATCATTGATTCCCTTGAGTGGTTA GACGATGCTATTATTGACGAGATTACACCCAAGCTGATCAGAGATTGGCCCAATATTTATACCTACACC AAGGCCTTGGGAGAAATGGTGGTGCAGCAAGAGAGCAGGAACCTGAACATTGCCATCATAAGGCCCTCC ATTGTGGGAGCAACTTGGCAGGAGCCTTTCCCAGGTTGGGTTGATAATATAAATGGACCTAATGGAATC ATTATTGCGACTGGGAAAGGGTTTCTTCGGGCCATAAAAGCTACTCCAATGGCTGTGGCAGACGTAATT CCAGTTGATACAGTCGTCAATCTCATGCTAGCTGTAGGATGGTATACTGCAGTTCACAGACCTAAGTCA ACATTAGTCTACCACATTACATCTGGTAACATGAATCCCTGCAATTGGCACAAAATGGGAGTCCAAGTC TTGGCAACCTTTGAAAAAATCCCATTTGAGAGACCTTTCAGGAGGCCAAATGCTAATTTTACCAGCAAC AGCTTCACATCACAGTACTGGAATGCGGTCAGCCACCGGGCCCCTGCCATTATCTATGACTGCTATCTG CGGCTCACTGGAAGGAAGCCCAGGATGACAAAGCTCATGAATCGGCTTTTAAGAACTGTTTCCATGTTG GAGTATTTCATCAACCGGAGTTGGGAATGGAGCACGTACAATACAGAAATGCTGATGTCTGAGCTGAGT CCTGAAGACCAGAGAGTATTCAACTTTGACGTGCGCCAGTTGAACTGGTTGGAATACATTGAAAATTAT GTTTTGGGAGTTAAAAAATACTTATTGAAAGAGGATATGGCTGGGATCCCAAAAGCAAAGCAACGCTTA AAAAGGCTCCGAAATATTCACTACCTCTTTAATACTGCCCTCTTCCTTATCGCCTGGCGCCTTCTCATT GCAAGATCTCAGATGGCTCGGAATGTCTGGTTCTTCATTGTAAGCTTCTGTTATAAATTCCTCTCCTAC TTTAGAGCATCCAGCACGCTCAAAGTTTAA |
Restriction Sites | SgfI-MluI |
ACCN | NM_001271783 |
Insert Size | 1548 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). |
Product Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
Reconstitution | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
Reference Data | |
RefSeq | NM_001271783.1 |
RefSeq Size | 3838 bp |
RefSeq ORF | 1548 bp |
Locus ID | 55711 |
UniProt ID | Q96K12 |
Protein Families | Transmembrane |
MW | 59.4 kDa |
Gene Summary | This gene belongs to the short chain dehydrogenase/reductase superfamily. It encodes a reductase enzyme involved in the first step of wax biosynthesis wherein fatty acids are converted to fatty alcohols. The encoded peroxisomal protein utilizes saturated fatty acids of 16 or 18 carbons as preferred substrates. Alternatively spliced transcript variants have been observed for this gene. Related pseudogenes have been identified on chromosomes 2, 14 and 22. [provided by RefSeq, Nov 2012] Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (1). Both variants 1 and 2 encode the same isoform (1). 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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