RIPX (RUFY3) (NM_001130709) Human 3' UTR Clone
CAT#: SC203944
3' UTR clone of RUN and FYVE domain containing 3 (RUFY3) transcript variant 3 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 | RIPX (RUFY3) (NM_001130709) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | RIPX; SINGAR1; ZFYVE30 |
ACCN | NM_001130709 |
Insert Size | 331 bp |
Sequence Data |
>SC203944 3’UTR clone of NM_001130709
The sequence shown below is from the reference sequence of NM_001130709. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTACCATTAAACAACTTGAACAAAGGTAAAAGTCCTGTTTCTTTAATGAAACACTTTGGATTGTCAGT GCTGAAGTGAAAAGAATGTGCTGTACATTCGGCAAATAGAAAATACATGAAATTCTTCCAAATTAGCAT CAGACATTCTGGTAGAAAAAAGCCAGTTGAATGTTATGTGTGTTTTCTAAGGTATGACTGAAATGTTTT TAGGAAATGTCAATCACTTGACTAGCCTTTAAAAAAAAAAAAGAAAGGTCAGCCTTTTATGACTGTTTT GAACATCAGAACTCTTAATCCATGTCAGAGTCATGTGTTAGAGGAAGGATACTTA 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_001130709.2 |
Synonyms | RIPX; SINGAR1; ZFYVE30 |
Summary | This gene encodes a RPIP8, UNC-14, and NESCA domain-containing protein that is required for maintenance of neuronal polarity. In addition, it has been implicated in mediation of gastric cancer cell migration and invasion via interaction with P21-activated kinase-1, which promotes its expression. The encoded protein localizes to F-actin-enriched invadopodia to induce formation of protrusions, thereby facilitating cell migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
Locus ID | 22902 |
MW | 13 |
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