SLC25A12 (NM_003705) Human 3' UTR Clone
CAT#: SC216816
3' UTR clone of solute carrier family 25 (mitochondrial carrier Aralar) member 12 (SLC25A12) nuclear gene encoding mitochondrial protein for miRNA target validation
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CNY 5795.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | SLC25A12 (NM_003705) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | AGC1; ARALAR; DEE39; EIEE39 |
ACCN | NM_003705 |
Insert Size | 1899 bp |
Sequence Data |
>SC216816 3’UTR clone of NM_003705
The sequence shown below is from the reference sequence of NM_003705. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCAAAGGCAGCAGTGGCAGCCACTCAGTGATGAGACAACTGTTGAGTGTGGCAAAATGGCGCCTTGAAG AAAGAGGCCTAGGAGAGCAGCCCTGTAATGTATCCAGTCAGCTGCATGGTACTGACTGAGCTGAGGAGT CAAACTCTTCTTTCTGTATGACATATACATATACTTGTTTATAAAATAATCATTTGCCCAGGGAAAAAA CCACAACGCTGTTTCAAGCTTTAGTCTTATGTGTTGAAATGTTTTTGTAAGCCTTGGCATGAATTAGTG TTCTAGACTCTGCTTTGCACAGCTTGCACTTACAGTGATTGTACATATTGTACATCTTTGTACAGAGAC ATCTTGGCACCTCATCCCAACAAATCACATTTGTAGAAATGTAATGCGGTTCTGAGTGGCTTGAAATGT ACAGAATGTTTTGAAAGTGTTTTATTAAGAATCACACAAAAATAAATGTATTAAAATTAAATTCATTCT CTTATTGGTGACTTATGGAAATAAAGCATCAATATTGGATGTATTTAATTCCTAGTTTGTTTTCCATTC TGGAATAAAAAGGTATTTGCTGATAAAAGGCATAACGAGACATAGTGCTGCTACCACTGAATAAGTGAT ACTTTGGAAAGATGCATGCCAGTGGATGCCAGAGGACCAGGCTAATGACTTGTGTGTGCTGATGTGTTT CCATTTGTATTTAATGTGTGTAGACCCTCCTCTGTTCATCAATCAAAAAGCATTTCCTAGGCAGCTCCT CGCCTGTCAGTGTGCATATGGAAACAGGGACATCTCCATCATTACTGGCTTAGTTTTGCTTTCCTTTGA CACAGTAAGGCAAAGGCCAAGCTTTCAAAAGAGTAAAGGATACTTTCACAATTTCCCTTCATATGGATA TGATTCCAGTCAAAAATAAAATGCACACCAAAATGTATACATGTAGTTGGATTTTTCTTTGTAAATATA CTGATAATACTTTTTGTTCTGATTGACTACTGATTGCAAATAACTCATGATCGGGTTCGCCCTTTCTTC CACCTTTATAGAAAACAGAAAAATTAGTTTTAGAAAGGGCTAGCGCAGAGTGAAGGGAGGGAAGAAGAA AGAGAAGAAAAGCTCTATATGGTGATTTAGTGGGGTCTAGGTTCTTACTTTGGAATCCAAATGCAAACT GTTCTAAAAGTCACTCATCAAGGGCGTGATTACTAATTTGGATCTAAACATAGATCTTGACAGCCACAT CTACACTTTGATATGGATGTGATTTGATGTGCAGTATCAGAATTTATTTACCTTACCAAAGTGCTCTGG GAAGACATTATTGCTACTGCCAGTAAGCTGGGATATGAGAATGTATGCAAATATTTTCAAGAGGCGAGC CTGGAGACAGACCAAGTTACTTAGTATCCTGCACAGTGCTCCTCGATTGATGGCTGACAGCCCTGTGAC TGCAACTGTAGGCTCCCTGGAGGCCCTCCAGGAACAAAAGAATTAGCTTTGAAAGCAAGTTATTTTCAA ATGTATTAGATTGGTCTCATGGGAGTGGAACAAATAATAATACAGTTGTTTTGCTACTACCACTTGTTA GAAATATATAAGTAGTCCATGGATATGTGATTACAAAAGAATCCTATGTATGTATCTAGAGTGAGATGG GAAAGTGTCCCGCTTACCCTCCTTCTACCTCCACCACTTCCTGGCCCAGAGGTAATCACTGCTAACAGG TTACAGCATGAATATGTAGTCTGTTTTTCATAACTCTATAGAAATATATGTACATATTTATATTTTAGA AACAGGATTATGTTATGTGTGTGTTATTCTGTGTCTTGCTTTTGTTCACTTAATGTGTTTTGGATATCT TTCCATGTCAGTTTATAAAGTTTTATTTTTAATGGC 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). |
Reference Data | |
RefSeq | NM_003705.5 |
Synonyms | AGC1; ARALAR; DEE39; EIEE39 |
Summary | This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012] |
Locus ID | 8604 |
MW | 73.2 |
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