MAGEA9 (NM_005365) Human 3' UTR Clone

Specifications

Product Data
Product Name	MAGEA9 (NM_005365) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CT1.9; MAGE9
ACCN	NM_005365
Insert Size	609 bp
Sequence Data	Insert Sequence (showhide) >SC207888 3’UTR clone of NM_005365 The sequence shown below is from the reference sequence of NM_005365. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTTTTGGGAGAGGAGCAAGAGGGAGTCTGAGCACCAGCCGCAGCCGGGGCCAAAGTTTGTGGGGTCAGG GCCCCATCCAGCAGCTGCCCTGCCCCATGTGACATGAGGCCCATTCTTCGCTCTGTGTTTGAAGAGAGC AATCAGTGTTCTCAGTGGCAGTGGGTGGAAGTGAGCACACTGTATGTCATCTCTGGGTTCCTTGTCTAT TGGGTGATTTGGAGATTTATCCTTGCTCCCTTTTGGAATTGTTCAAATGTTCTTTTAATGGTCAGTTTA ATGAACTTCACCATCGAAGTTAATGAATGACAGTAGTCACACATATTGCTGTTTATGTTATTTAGGAGT AAGATTCTTGCTTTTGAGTCACATGGGGAAATCCCTGTTATTTTGTGAATTGGGACAAGATAACATAGC AGAGGAATTAATAATTTTTTTGAAACTTGAACTTAGCAGCAAAATAGAGCTCATAAAGAAATAGTGAAA TGAAAATGTAGTTAATTCTTGCCTTATACCTCTTTCTCTCTCCTGTAAAATTAAAACATATACATGTAT ACCTGGATTTGCTTGGCTTCTTTGAGCATGTAAGAGAAATAAAAATTGAAAGAATAA 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_005365.5
Synonyms	CT1.9; MAGE9
Summary	This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]
Locus ID	4108
MW	23.2

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