PAX3 (NM_181457) Human 3' UTR Clone
CAT#: SC202403
3`UTR clone of paired box 3 (PAX3) transcript variant PAX3 for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | PAX3 |
Synonyms | CDHS; HUP2; WS1; WS3 |
ACCN | NM_181457 |
Insert Size | 237 bp |
Sequence Data |
>SC202403 3'UTR clone of NM_181457
The sequence shown below is from the reference sequence of NM_181457. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GGACAAAGTAAGCCTTGGACTTTTTAGGGGGCAATTTCTCCTGGAAGGGAGATAAACTCAACTCTTCCTT AAGAAAGGTGAATTAGAGGCAAGATTAAGCCACACATGCCGGTATCAATTTTTTTTTTTTTTTGCAAAGC CAGCTGACTGTTCCAGCAGGGGCTTCCTTGTGTAATTATTTTCTTAACTGATGTCAACAACATCTTGCGG TTATTAATTGTTGAGACGTGAAACCTG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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). |
Product Components | The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. |
Reference Data | |
RefSeq | NM_181457.2 |
Summary | 'This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]' |
Locus ID | 5077 |
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