DNAAF4 (NM_001033559) Human 3' UTR Clone
CAT#: SC205228
3' UTR clone of dyslexia susceptibility 1 candidate 1 (DYX1C1) transcript variant 2 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 | DNAAF4 (NM_001033559) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CILD25; DYX1; DYX1C1; DYXC1; EKN1; RD |
ACCN | NM_001033559 |
Insert Size | 418 bp |
Sequence Data |
>SC205228 3’UTR clone of NM_001033559
The sequence shown below is from the reference sequence of NM_001033559. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAATTGATGCTGAGAAGATTCGGAATGTAATTCAAGGAACAGAACTAAAATCTTAATGACTATTAGAAG TAACTAAGTATTGTTATAAGTTTTTTAAAAACAACTGGAGGCATCTTTGTACATATTATGGCCAGTTGT ACAGAATCGCTTTCTGTTTAGTACTTTAGTTCTGTTGAGGGCAAAATATTATAAATCTATAGAAAATAA ACTGTTTGACTTGAATCATTTCTGAATAAGTAAATCTAAATAAGAATCTATTTTAATTCCTTATTTCTT CATATTAATACATATGTATACTTTTTTGTGTTACTGAATTAAGCTTGCCCTTGTAACAAAATATGTTTT GGTATAGTTACCAGGACACTTACTGATTAATTTTTAACAAGGTAGAATTTTAAAATAAAAGATTTATAA ATAA 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_001033559.3 |
Synonyms | CILD25; DYX1; DYX1C1; DYXC1; EKN1; RD |
Summary | This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011] |
Locus ID | 161582 |
MW | 16.3 |
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