HEAB (CLP1) (NM_001142597) Human 3' UTR Clone
CAT#: SC206033
3' UTR clone of CLP1 cleavage and polyadenylation factor I subunit homolog (S. cerevisiae) (CLP1) transcript variant 2 for miRNA target validation
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CN¥ 4,845.00
货期*
3周
规格
Product images
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经常一起买 (2)
Specifications
Product Data | |
Product Name | HEAB (CLP1) (NM_001142597) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | hClp1; HEAB |
ACCN | NM_001142597 |
Insert Size | 459 bp |
Sequence Data |
>SC206033 3’UTR clone of NM_001142597
The sequence shown below is from the reference sequence of NM_001142597. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGGATATCCGGTTCATGGATCTGAAGTAGAGATCAGCAGGAAGCCTTGCTGCCTGGGACATAGAGATC ATCTGGCCACCCCTAGAGGCAGATGGGCTGAGATAAAAGACTGTTGGGGCCACCTGACCAGTAAACTGT GGACTAGTAGAAAGTTCATATTCTACCTCTAAAAACAGGTAGTGGTAACCTGACTCTTCTAATCTTGAA CCAAAAGGAAAACCATGAGACTGTAATTGGTTTCTTAGACCACCTAAGATGCCACTTTGAATTCTCTAA GACCCTGGAGAATTGCATTTCTTTCACTGTGCTACTATGTGGTTTTTAAAAAATCAATGCTTTATATTC CATATGTGGTTCTTACCCATTTATCTAGGATGAAAGTGTGAATTAGAGGGACTCCTTCCAATAAAGTTC AAACTTAAAAAAAATCATTTTAATAAATATTTTTGCCATATCATA 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_001142597.2 |
Synonyms | hClp1; HEAB |
Summary | This gene encodes a member of the Clp1 family. The encoded protein is a multifunctional kinase which is a component of the tRNA splicing endonuclease complex and a component of the pre-mRNA cleavage complex II. This protein is implicated in tRNA, mRNA, and siRNA maturation. Mutations in this gene are associated with pontocerebellar hypoplasia type 10 (PCH10). Alternatively splice transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014] |
Locus ID | 10978 |
MW | 17.9 |
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