PAX3 (NM_000438) Human 3' UTR Clone

Specifications

Product Data
Product Name	PAX3 (NM_000438) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CDHS; HUP2; WS1; WS3
ACCN	NM_000438
Insert Size	500 bp
Sequence Data	Insert Sequence (showhide) >SC206413 3’UTR clone of NM_000438 The sequence shown below is from the reference sequence of NM_000438. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGGGTGACTTGGAGGGCATCGGCTAGCTGACATTGGTGATCTGACGGCAGCCAAGCCCAGCTCGGATCA AGGTCCCTTCATGCGCGGTGTCTCTGCGCCTGAGTAACGACATGGAACTGAAAGACCAGAGGGACACTA GGAATCAAAACAAACATTTCTATTCTGCTTAGTTTTTCTGTTTTGTAAATCTTTCTTTCTTAACCACTT TCAGCCCCTGGGATTCTAGAACTGTGAATTGTGCTCTGTTGTAGGGGGCAGGGGAAGCTCTCACTCTGT TGCCATTAAATGTATGAGACTGGGCATCTCTGAGCAATTGTAGGGCCGGGGATAGAGGGTACTTGAATC TTCAGAAGTTGAAGTAGCTTTTATGCCCTCAGGAAAGGCCCTGGTCTCCGGAGTTTCCTCGCATTAAAG GAGAGAGAGAGAGAGTACTCTTTTGGGCAACGGCCCTCCAAAATTGCCCCCACATTGGCTGCCTTATAA ATATGTCTGTGTGTTGA 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_000438.6
Synonyms	CDHS; HUP2; WS1; WS3
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
MW	18.2

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