Aprataxin (APTX) (NM_175071) Human 3' UTR Clone
CAT#: SC210988
3`UTR clone of aprataxin (APTX) transcript variant 5 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 | APTX |
Synonyms | AOA; AOA1; aprataxin; ataxia 1, early onset with hypoalbuminemia; AXA1; EAOH; EOAHA; FHA-HIT; FLJ20157; MGC1072; OTTHUMP00000021188 |
ACCN | NM_175071 |
Insert Size | 887 |
Sequence Data |
>SC210988 3'UTR clone of NM_175071
The sequence shown below is from the reference sequence of NM_175071. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC ACATCTCAGGAAGCACTGGACACAGTGATTCTGCAGAGCCTGAGCTGCTGCTGTGGTGTGGCCCACTGGA GCAAACTGCTGGCACCTATTCTGGGTTGCTTGTGAACTTCTACTCATTTCCTAAATTAAAACATGCAGCT TTTTCACAAATTTATTCTATTATTGAGTGGCCACAATGTAGAGTGGCTCAAAGTACTTCAGGATTAGGAA TTTGGGTTTGTCATAGATGTATTCTCTGGTGAGGGTGGCTGGGATATACCTGACCCACCATCTTCAGAAG GACCCATGTCAGGTCTGACCATTGGGAGCAAAGCCATGTTCACACTGACCTAATGCAGAGTATGGAAGCA TTGGGCTGGTTATACATTTCTGTTTCTTAGATTTATCCTCCGCCTCTGTAGGCATGGACAACCTTTAATC AGAGCATCTAGAGTGGCCTCTTGTTTATCCTGAAGATACTGATGGGTCTTGTTTTCTGTTAGTCTGTTTT GTAATATTCTTTTCCCTTCCTTCATGGGGAGGCTTAGTTTGTCCAGTCCTTCCATGCCCTTCTATCCCAG ATTACCTAAATGTTCCCTTCTCAGGAATTCTGTCTCATCAGTTCTTCACAGTGAGAAAAGAGGCTAGATG ATGGTGTGGGGGGTTGGAGTTTTCTTCTAATACCGAGGGTTCCTGGCTGTGAGGAAACAGCCACATGTTC GTCATGATTGAGCTGTGAAGTCTTCTTGGACCTGTTGTCTGAAAATAAAGTTAATTTGTTTGAGGCATCT CTCTTAAGTAGGTGGAAACTATTGAAGTTCAGCTAACAATCACAGCATAGGTTCTGATGCATGGAAAGGT GGTTGGTGAATGAAAAAGTTGCGTAGAGCCACTACTTTCTTTTTCCC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_175071.1 |
Summary | This gene encodes a member of the histidine triad (HIT) superfamily. The encoded protein may play a role in single-stranded DNA repair through its nucleotide-binding activity and its diadenosine polyphosphate hydrolase activity. Mutations in this gene have been associated with ataxia-ocular apraxia. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010] |
Locus ID | 54840 |
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