myosin heavy chain 3 (MYH3) (NM_002470) Human 3' UTR Clone
CAT#: SC201193
3' UTR clone of myosin heavy chain 3 skeletal muscle embryonic (MYH3) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | myosin heavy chain 3 (MYH3) (NM_002470) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CPSFS1A; CPSFS1B; CPSKF1A; CPSKF1B; DA2A; DA2B; DA2B3; DA8; HEMHC; MYHC-EMB; MYHSE1; SMHCE |
ACCN | NM_002470 |
Insert Size | 151 bp |
Sequence Data |
>SC201193 3’UTR clone of NM_002470
The sequence shown below is from the reference sequence of NM_002470. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGGATGGTGGTCCACGAGAGTGAAGAGTGAGCCAGCCCTTCTGGAGCAGGACAGAAGATATGCAAAATG TATATTTTCTTGATTCCTGACCATTGATACTTAATGTCCATGTGACTCTTTTTCACATGCAATAAACTT TGCTTTGTTTCAA 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_002470.4 |
Synonyms | CPSFS1A; CPSFS1B; CPSKF1A; CPSKF1B; DA2A; DA2B; DA2B3; DA8; HEMHC; MYHC-EMB; MYHSE1; SMHCE |
Summary | Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008] |
Locus ID | 4621 |
MW | 5.8 |
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