ASC1 (TRIP4) (NM_016213) Human 3' UTR Clone
CAT#: SC203164
3' UTR clone of thyroid hormone receptor interactor 4 (TRIP4) 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 | ASC1 (TRIP4) (NM_016213) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ASC-1; ASC1; HsT17391; MDCDC; SMABF1; ZC2HC5 |
ACCN | NM_016213 |
Insert Size | 269 bp |
Sequence Data |
>SC203164 3’UTR clone of NM_016213
The sequence shown below is from the reference sequence of NM_016213. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGGTTAATGAAGCAGAATAAAGCTGTCTGACCCAGGAGAAAAGGAACTATACAGCATAGTGGAGTTTTG TGTACTAAAATTGCTATCTACTGGTCCTTTGGAATTGAAGTAGTAGAAACCTAAAGGCTTGGCGTCAGG CTTGAATATCTCAGAACTTAAACTCTTACCAAAATCTGTATATTTTTCTTAAGGAGTGGGATTCCTACT TTATGTAATGGGGTCGAAATCTTTGAACACATTATTTATAAAAACCTGTTTAAAAATTCTAA 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_016213.5 |
Synonyms | ASC-1; ASC1; HsT17391; MDCDC; SMABF1; ZC2HC5 |
Summary | This gene encodes a subunit of the tetrameric nuclear activating signal cointegrator 1 (ASC-1) complex, which associates with transcriptional coactivators, nuclear receptors and basal transcription factors to facilitate nuclear receptors-mediated transcription. This protein is localized in the nucleus and contains an E1A-type zinc finger domain, which mediates interaction with transcriptional coactivators and ligand-bound nuclear receptors, such as thyroid hormone receptor and retinoid X receptor alpha, but not glucocorticoid receptor. Mutations in this gene are associated with spinal muscular atrophy with congenital bone fractures-1 (SMABF1). [provided by RefSeq, Apr 2016] |
Locus ID | 9325 |
MW | 10.2 |
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