MYH14 (NM_001077186) Human 3' UTR Clone

Specifications

Product Data
Product Name	MYH14 (NM_001077186) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DFNA4; DFNA4A; FP17425; MHC16; MYH17; myosin; NMHC-II-C; NMHC II-C; PNMHH
ACCN	NM_001077186
Insert Size	780 bp
Sequence Data	Insert Sequence (showhide) >SC209738 3’UTR clone of NM_001077186 The sequence shown below is from the reference sequence of NM_001077186. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGGGGTCCCCACCAGCCCACCCCCAGTGACCCTACCCTGTCCCCAGATGCACTAACAGATGGGGCCCA GCCCCCTTCCTCCCTGGACCCCACGGGCCCCTGTCCCAGGAACCCCGCCCTCTGACTTCTTGCCCTTTG GAAATGGTGCAGCACTCTGGCATTTATCACCCCCACCTGGGTCCCCTGCAACCTCCCATCAAAGGATGA CCCCTAAACACAGAGGAGCGGGGCAGGCAGGGAGGCAATGACTGGAGCTACCTTGCTTGTTGGGGGACT GGGTACAGTTGGCAAGCTGTGTTTCCATCAGCTCCCTGTCCTCCTTTCTTCCCTCGTTATTGATCTATA GACATTAGGAAGGGAGTGAGACGGCTCCTCCACCATCCTCAGCCAGTGCAACCCATTCCCTCTGCTTCT CTCTCTCTCTCTCTCTCTCCCTCCCTCTCCTTCCCTACCCTCTCACCATCTTTCTTGGCCTCTCTGAGG GTCTCTCTGTGCATCTTTTTAGGAATCTCGCTCTCACTCTCTACGTAGCCACTCTCCTTCCCCCATTTC TGCGTCCACCCCTGAACTCCTGAGCGACAGAAGCCCCAGGCCTCCACCAGCCTTGAACCCTTGCAAAGG GGCAGGACAAGGGGACCCCTCTCACTCCTGCTGCTGCCCATGCTCTGCCCTCCCTTCTGGTTGCTCTGA GGGTTCGGAGCTTCCCTCTGGGACTAAAGGAGTGTCCTTTACCCTCCCAGCCTCCAGGCTCTGGCAGAA ATAAACTCCAACCCGACTGGA 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_001077186.2
Synonyms	DFNA4; DFNA4A; FP17425; MHC16; MYH17; myosin; NMHC-II-C; NMHC II-C; PNMHH
Summary	This gene encodes a member of the myosin superfamily. The protein represents a conventional non-muscle myosin; it should not be confused with the unconventional myosin-14 (MYO14). Myosins are actin-dependent motor proteins with diverse functions including regulation of cytokinesis, cell motility, and cell polarity. Mutations in this gene result in one form of autosomal dominant hearing impairment. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Locus ID	79784
MW	28.5

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