Coiled coil domain containing protein 111 (PRIMPOL) (NM_152683) Human 3' UTR Clone
CAT#: SC201890
3' UTR clone of coiled-coil domain containing 111 (CCDC111) for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | Coiled coil domain containing protein 111 (PRIMPOL) (NM_152683) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CCDC111; MYP22; Primpol1 |
ACCN | NM_152683 |
Insert Size | 203 bp |
Sequence Data |
>SC201890 3’UTR clone of NM_152683
The sequence shown below is from the reference sequence of NM_152683. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAACTAATTATAGAAGTATTACAAGAGTAACTAATTCACTATGAACACTTTTGTCACCAGGCTATAATT TGCCTGATGTCTGTGAGATTTGATAAATATATCATTCAACCTGTTTATATAAACTAAGTTTTATTACTT TGCTTTCCAATTTTTGTTTTTTACTTCTGTAAACCAATTTCATTAAAAATTAGCTTTGGTGTAAA 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_152683.4 |
Synonyms | CCDC111; MYP22; Primpol1 |
Summary | This gene encodes a DNA primase-polymerase that belongs to a superfamily of archaeao-eukaryotic primases. Members of this family have primase activity, catalyzing the synthesis of short RNA primers that serve as starting points for DNA synthesis, as well as DNA polymerase activity. The encoded protein facilitates DNA damage tolerance by mediating uninterrupted fork progression after UV irradiation and reinitiating DNA synthesis. An allelic variant in this gene is associated with myopia 22. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
Locus ID | 201973 |
MW | 8 |
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