WDR62 (NM_001083961) Human 3' UTR Clone
CAT#: SC200388
3' UTR clone of WD repeat domain 62 (WDR62) transcript variant 1 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 | WDR62 (NM_001083961) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C19orf14; MCPH2 |
ACCN | NM_001083961 |
Insert Size | 110 bp |
Sequence Data |
>SC200388 3’UTR clone of NM_001083961
The sequence shown below is from the reference sequence of NM_001083961. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCGTGCGGAGGAAGGCACGGGGGCACTGAGGGCGCAGCCCCTCCACCGCAGCCCTGCTGCTTCTGAGG ACTTAGGTATTTTAAGCGAATAAACTGACAGCTTTGAGGAA 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_001083961.2 |
Synonyms | C19orf14; MCPH2 |
Summary | This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011] |
Locus ID | 284403 |
MW | 4 |
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