MYBPC3 (NM_000256) Human 3' UTR Clone
CAT#: SC204472
3' UTR clone of myosin binding protein C cardiac (MYBPC3) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | MYBPC3 (NM_000256) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CMD1MM; CMH4; cMyBP-C; FHC; LVNC10; MYBP-C |
ACCN | NM_000256 |
Insert Size | 367 bp |
Sequence Data |
>SC204472 3’UTR clone of NM_000256
The sequence shown below is from the reference sequence of NM_000256. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGCCGCCTGGAGGTGCGAGTGCCTCAGTGACCAGGCTGGCTCCTGGGGATGGCCAGGTACAACCGGATG CCAGCCCCGTGCCAGGAGCCTGGAGGGAAGTTGGGGAAACCCCTCCCTACTGTTGGATGTATGTGTGAC AAGTGTGTCTCCTGTGCTGCGATGGGGGATCAGCAGGGCAGTTGTCGGGCAGTCCTGAGTGGGTGTTGC ACAGACTGGTCCACAGGGCTCCTGAAGGAAGCCCCTGGATCTTTGGGGTAAAAGGAGGGTGGCCTCAAG AAACAATGTCTGGGGACAGGCCTTTCTGGCCTGCTATGTCTTCCCAATGTTTATTGGGCAATAAAAGAT AAGTGCAGTCACAGAGAACTCA 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_000256.3 |
Synonyms | CMD1MM; CMH4; cMyBP-C; FHC; LVNC10; MYBP-C |
Summary | MYBPC3 encodes the cardiac isoform of myosin-binding protein C. Myosin-binding protein C is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. MYBPC3, the cardiac isoform, is expressed exclussively in heart muscle. Regulatory phosphorylation of the cardiac isoform in vivo by cAMP-dependent protein kinase (PKA) upon adrenergic stimulation may be linked to modulation of cardiac contraction. Mutations in MYBPC3 are one cause of familial hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008] |
Locus ID | 4607 |
MW | 13 |
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