NIPA2 (NM_001008892) Human 3' UTR Clone
CAT#: SC210869
3' UTR clone of non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2) transcript variant 3 for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | NIPA2 (NM_001008892) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | SLC57A2 |
ACCN | NM_001008892 |
Insert Size | 1567 bp |
Sequence Data |
>SC210869 3’UTR clone of NM_001008892
The sequence shown below is from the reference sequence of NM_001008892. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGAAGAAATGGAAATCTGACAGCTTTTTAAGAAAGGTGTAATTAAAGGTTAATCTGTGATTGTTATGAA GTGAATTTGAATATCATCAGAATGTGTCTGAAAAAACATTGTCCTCAAATAATGTTCTTTAAAGGCAAT CTTTTTAAAGATTTCACTAATTTGGACCAAGAAATTACTTTTCTTGTATTTAAACAAACAATGGTAGCT CACTAAAATGACCTCAGCACATGACGATTTCTATTAACATTTTATTGTTGTAGAAGTATTTTACATTTT CATCCCTTCTCCAAAAGCCGAATGCACTAATGACAGTTTTAAGTCTATGAAAATGCTTTATTTTTTCAT TGGTGATGAAAGTCTGAAATGTGCATTTGTCATCCCCACTCCATCAATCCCTGACCATGTAAGGCTTTT TTATTTTAAAAAAACAGAGTTATCCCAATACATTATCCTGTGATTTACCTTACCTACAAAAGTGGCTCC TGTTTGTTTGATGATGATTGGTTTTATTTTTGAAATATTTATTAAGGGAAAACTAAGTTACTGAATGAA GGAACCTCTTTCTTACAAAACAAAAAAAAGGGCAGAAATCACCCCAAGGAACGATTTCTCAGGTTGAGA TGATCACCGTGAATCCGGCTTCCTCTGAGCATTCGATGGCCTTAGCACCTCATCAAGCCAGCACATCCT GCCTGCTGTTGCAGCCTGGCTGGGTTTATTCTTCAGTTACCCTAATCCCATGATGCCTGGAACCTTGAT TACCGTTTTACATCAGCTCTTGTACTTTTCAGTATATTTTCATAATGAGTTATATTGTCATTTAGACTT TGAACAGCTCTGGGAAATAGAAGACTAGGGTTGTTTCTTAAATTTAGCTCATGTTATAATAAAAAGTTG AAATGAAGTTCTTATTCTAAAAGTCTGAATGCTTAGAACAAACTTAACATGTTTATAGAATATGGTCTC TTTGTACCAAGTACTTTGCTTAAGAGCTCCTTTGGGCCACTACATATTTTGGTTTCTAGAAAATGTTTG TTTATGAAGAAGTCGATGGAAAACTGCAAACATATGCAGAAAAGGTAGAATAATAAAAAAGGTCTAATG AACTCCATTCAGCTTTGAACCTATCCACTCATAACCATTGACTGGCCTTTAAAAAAAAGTATTGGCAGA ATTAATTTCCACCTAGGTGATGGGAAGAAAGTGTTCGCCTGTTCCAGCCTGTGGCTCCTGCCTGGAGGT TACCCAGTGGTGCGCCAGCGCCAAGCCATCACTCCCCGAGGGCCTCCCCTGCCAATGGTGCTGGTATCC CATGCAGCTCACCACTGGCTGCGTGGAAACTCCCTTTTTTCCAACTTTATTATTGGCCTTCTAAGGAGC TGTTTTAGATGTTTTTTCTAACTGCCTCCTCCCATGCCATTTTAATACTACAGATGTACTACGTATCTG TTTATATACTGTACCTACATCTGTGCTTTGTACATAAAAGAACCAGTTTTCTCCCCCTTGAGGACAGAG ACTCATTTGAACATGCATAGGTTAATAAATAATAAATTCTTATTTAACA 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_001008892.3 |
Synonyms | SLC57A2 |
Summary | This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010] |
Locus ID | 81614 |
MW | 61.3 |
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