Dystrophin (DMD) (NM_004019) Human 3' UTR Clone

Specifications

Product Data
Product Name	Dystrophin (DMD) (NM_004019) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BMD; CMD3B; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; MRX85
ACCN	NM_004019
Insert Size	500 bp
Sequence Data	Insert Sequence (showhide) >SC206377 3’UTR clone of NM_004019 The sequence shown below is from the reference sequence of NM_004019. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCTTAGAGGGGGACAACATGGAAACGTGAGTAGTAGCAAAAGCAGAACACACTCTTGTTTGATGTATA TTTGAACTCCTCTCAGCTGAACACCCTCCTTCACTCCCAAATGCAAACAGTCTCTTCTATTTCTTTCTT TTTATTTACATTAGCTGAAAAGAGAAAAATAAGCTGATGTCCAGTTGCCACTTTCCCACGTCACTTGAC AATTTCTTTTTCCAAAAGTTAAACTTTATCTCACAGGGGGAAAAAAAAAAAAAAACCACAACACAATAC AGCCACTAATTGCCTTACAAGCCTTATAAGAAATATGGGACTGTTTACAAATGAGTGATTCCAGTATTT CATTTTGATTTTCCTCTCTCACAAATCAGTAAATGTGTGTCTTTTTGTATCTCATTGTGTGGTCATATC TAGTCACTTGTTTCTACTCAAAAGAAAATATAGTCACAGGAAACTACTTCACAGTAAGTAGTAATGATT CTCAAGATCAAAGGGGA 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_004019.3
Synonyms	BMD; CMD3B; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; MRX85
Summary	This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [provided by RefSeq, Dec 2016]
Locus ID	1756
MW	19

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