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
    • 10 ug

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DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1280.00

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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