Myotilin (MYOT) (NM_001135940) Human 3' UTR Clone
CAT#: SC206542
3' UTR clone of myotilin (MYOT) transcript variant 2 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 | Myotilin (MYOT) (NM_001135940) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | LGMD1; LGMD1A; MFM3; TTID; TTOD |
ACCN | NM_001135940 |
Insert Size | 496 bp |
Sequence Data |
>SC206542 3’UTR clone of NM_001135940
The sequence shown below is from the reference sequence of NM_001135940. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCTGGACTCTATGAAAGTGAAGAACTTTAATAACTTTACCAACATTGGAAAACAGCCAACTACACCATT AGTAATATATTTGATTACATTTTTTTGAAATTAATCCATAGCTGTATTAACAGATTATGGTTTTAATTA GGTAATATAGTTAATATATATTTATAATATTATTTATCCTTTGACTCTTGCACATTCTATGTACCCCTC CGATTTGTGAAGCCTACAGGAAATCTGGGTATATGGATTTGTAACTGCAGAAGACTATCTTAAAATACA GGATTTTAACATTTAAGTCATGCACATTTAACAATTACAGGTTATAAATTAGTATCAACTTTTTAAACA CATCTAATGCTTGTAATAACGTTTACTGGTACTGCTTTCTAAATACTGTTTTACCCGTTTTCTCTTGTA GGAATACTAACATGGTATAGATTATCTGAGTGTTCCACAGTTGTATGTCAAAAGAAAATAAAATTCAAA TATTTAAAACGGA 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_001135940.2 |
Synonyms | LGMD1; LGMD1A; MFM3; TTID; TTOD |
Summary | This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.[provided by RefSeq, Oct 2008] |
Locus ID | 9499 |
MW | 19.5 |
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