Troponin T1 (TNNT1) (NM_001126132) Human 3' UTR Clone
CAT#: SC201127
3' UTR clone of troponin T type 1 (skeletal slow) (TNNT1) 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 | Troponin T1 (TNNT1) (NM_001126132) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ANM; NEM5; STNT; TNT; TNTS |
ACCN | NM_001126132 |
Insert Size | 247 bp |
Sequence Data |
>SC201127 3’UTR clone of NM_001126132
The sequence shown below is from the reference sequence of NM_001126132. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAGGGCCGCGTTGGAGGCCGCTGGAAGTGAGGATGCCGCCCCGGACAGTGGCACCTGGGAAGCCTGGGA GTGTTTGTCCCATCGGTAGCTTGAAATAAACGCTCCCCTCAGACACCCGCTGGGTTCTCTGATGTTATT ATGGTTGAGATGCAGCTGGTCTCTCCTGGTTAATTGACTTCTTATTACCAACAAGTTACTTGAAAGAGT GTCACCAATAATCATTAAAGTACGGCAGGCTGAACCTTCA 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_001126132.3 |
Synonyms | ANM; NEM5; STNT; TNT; TNTS |
Summary | This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Locus ID | 7138 |
MW | 8.9 |
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