MAGEE1 (NM_020932) Human 3' UTR Clone

Specifications

Product Data
Product Name	MAGEE1 (NM_020932) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DAMAGE; HCA1
ACCN	NM_020932
Insert Size	568 bp
Sequence Data	Insert Sequence (showhide) >SC207527 3’UTR clone of NM_020932 The sequence shown below is from the reference sequence of NM_020932. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGGCAAATCTTTGTTCACAACTTCAGGTAGAGGAATGCATGGCAGTCAGAGGGGCCTTGCAAGGAGGGG CCTTTGAGCCTCAGTTCTCATGTATTGGGGGGTGGGGGTGGGTACATATTGTATTTGGTATTTGTGTTC CAGTTATATTTATGTCTTTTCATATTTAGTTCTGGTGTGGTGTCTGGAAATGTTTCAACTGTTTTAATA TATTGTCTGATTGGGTAAATGTGATTGACCACTTGCTGTCTCTGTTGTATTTTGGTATGAGTTTTGATA GCTCTATAAAATGTTTTGGAAATCTTTCCATCTTGTTGCATTATCTAGAAAAGAATATAGCATATAGCT ATAGATATAGGCTTTTCCTTGAAAGCTTGAAAAAAATTCGCCAGTAAAATAATCTAGCTTAAAGTGATA AACTAACAAACAAATATAACAACAACTGAAAAGGCACTCTAAATTGTGGCTGGCTTCCCTTTCTGTCTG CTATTGTATGAAGAATACTGATGTTTACCTGTATTTGCTTTGCTGTACTAAAATGTAATGAAAAATAAA AGATTAATAAATGAAA 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_020932.3
Synonyms	DAMAGE; HCA1
Summary	This gene encodes an alpha-dystrobrevin-associated MAGE (melanoma-associated antigen) protein, which is a member of the MAGE family. The protein contains a nuclear localization signal in the N-terminus, 30 12-amino acid repeats beginning at nt 60 with the consensus sequence ASEGPSTSVLPT, and two MAGE domains in the C-terminus. It may play a signaling role in brain, muscle, and peripheral nerve. This gene is located on X chromosome in a region containing loci linked to cognitive disability. [provided by RefSeq, Mar 2010]
Locus ID	57692
MW	21.2

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