CMH1 (MYH7) (NM_000257) Human 3' UTR Clone

CAT#: SC201064

3' UTR clone of myosin heavy chain 7 cardiac muscle beta (MYH7) for miRNA target validation



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CNY 4845.00


货期*
3周

规格
    • 10 ug

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Specifications

Product Data
Product Name CMH1 (MYH7) (NM_000257) Human 3' UTR Clone
Vector pMirTarget
Synonyms CMD1S; CMH1; MPD1; MYHCB; SPMD; SPMM
ACCN NM_000257
Insert Size 144 bp
Sequence Data
>SC201064 3’UTR clone of NM_000257
The sequence shown below is from the reference sequence of NM_000257. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
ATTGGCACGAAGGGCTTGAATGAGGAGTAGCTTTGCCACATCTTGATCTGCTCAGCCCTGGAGGTGCCA
GCAAAGCCCCATGCTGGAGCCTGTGTAACAGCTCCTTGGGAGGAAGCAGAATAAAGCAATTTTCCTTGA
AGCCGA
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_000257.4
Synonyms CMD1S; CMH1; MPD1; MYHCB; SPMD; SPMM
Summary Muscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy. [provided by RefSeq, Jul 2008]
Locus ID 4625
MW 5.1
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