WNK1 (NM_213655) Human 3' UTR Clone
CAT#: SC206727
3' UTR clone of hereditary sensory neuropathy type II (HSN2) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | WNK1 (NM_213655) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | HSAN2; HSN2; KDP; p65; PPP1R167; PRKWNK1; PSK |
ACCN | NM_213655 |
Insert Size | 2000 bp |
Sequence Data |
>SC206727 3’UTR clone of NM_213655
The sequence shown below is from the reference sequence of NM_213655. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCCCAGGCTCCAACCTGCGGACCACTTAGACCTAGAGACATTAACTGAATAGATCTGGGGGCAGGAGA TGGAATGCTGAGGGGGTGGGTGGGGGTGGGAAGTAGCCTATATACTAACTACTAGTGCTGCATTTAACT GGTTATTTCTTGCCAGAGGGGAATGTTTTTAATACTGCATTGAGCCCTCAGAATGGAGAGTCTCCCCCG CTCCAGTTATTGGAATGGGAGAGGAAGGAAAGAACAGCTTTTTTGTCAAGGGGCAGCTTCAGACCATGC TTTCCTGTTTATCTATACTCAGTAATGAGGATGAGGGCTAGGAAAGTCTTGTTCATAAGGAAGCTGGAG AACTCAATGTAAAATCAAACCCATCTGTAATTTCGAGTGGGTGGAGCTCTTGCTTTTGGTACATGCCCT GAATCCCTCACTCCCTCAAGAATCCGAACCACAGGACAAAAACCACCTACTGGGCTCTCTCCTACCCTG CCCTCCTCCCTTTTTTTTACCCCTCTCTTTTTTATTTTTTCTTTGCTCTTTAGAACCCAGTGAAAAATA CCAGGGTACTGGGGTGCAACTCTTTCTTATGATAGGTCATTAGTGCTTTAAGCAAAAGATATTAGCAGC TTTGACTGCAGCATTAGCAATTAGGAAAAAAAAAAAATTAAGTTCCCTGCGGACATGTAACTTTGCCAT CAGTTTTGATGTGGAAACACTGTGATATATAAAATGTTGTTGGACAACAGTAGTTTTAAGAGTAAAATA TGAAACGTTTAAAAAGTTCCAAAAAAAGCTAGCTCTGTCCTTTACTTATTGAGACACTTTAACTTTTTC CTTTGTATTTCCATTGTATTAGATAAATAAATGTGAATGTAAAATTGTATAAATTACTGTACTTGAATA CTTCTGTTTCCCAGTGTTGCTTGCTGGACATTTTAGTGCCTTGGACTTCTATTGCTTCTGCCATTAGCA TCAACTTACCAGACCCCAGATCAATAAAGGGCATGTGGAAGGAAATCGTAGGTCCATGTGACCCCAGCA GTCCAGCAGTGGTTATGCCAAAGGGAAATTGAAAAAGTATTTTTTTAAGTCATTCAACAACTTTGTCTA GAGCAGGTGTAAGATGAGTAGGGTGGGAAGTTAGGTTGGCATCAGTGGTTAAAAACAGAAAGTTCTGTT TCGGGAATAGTGAGGAGGGGGTGTTGTAACAAAATTGGACAACTTAAAAGAATGGTGTGTGCTGGGTGA AAGACAAAGACTAAAGAATGAGGAAACAAACGTGATGCCTGGCCAGTGACTGTCATATAAACCTTTCTT ATTTGAGCTAGGCTTGAACAGACGTGACCTAGAAGAAACTGAACATAAAGAGAAGGGGGTGGGGGGCTA GTTTTCAAGTTGGGGAACCTGATAGTGAAAAGTCACAGATGGAGAAAATTGCTCTCAGAAAAACTGTTT GGATTGCTTTCCTCTTGTTGCACATGTACCATGCATTTCTCAGCTTGGGGTACTACATTTTGTGGAAAG TTAATCTATCTATCTTTCCACATCTGAATTAATCATTCTAGGAAAGAATACTTATTCCTACTCATTTCC TTTATGATGTCCAAATGGTTGCAGGATCATAATCTATTGTGCCACCTTTATTTCTAGAAGTACAACTAA TATGTTCACATTTTCAAATAAATAATACTCCCCGTAAGTAATAACTGCAACCAATCAGTGTTATTCAGT GCTATGCCTCCTTGTAATGGGTAGTTATTAATTATTTTCAGAGCTTTCCGGAAATACTGTCCTAACTGG CTATGTTTAGGATCTTTGTTATCTCTGAAGACAAAGAAAGAAGCTAGGACTCTTAATTTTGGGGTGCTT CTTGACTCTTAGTTGGGAAACTGAAAATATTTCCAACCTTTTACCCACGTCAATGGCATATTCTGGGAA TCACCACCACCACCACCACTACCACAGAAAGAGGCTGGAGGCTCCTGTACCCTGTTCATTCCTTAAGG 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_213655.5 |
Synonyms | HSAN2; HSN2; KDP; p65; PPP1R167; PRKWNK1; PSK |
Summary | This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010] |
Locus ID | 65125 |
MW | 75.8 |
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