Troponin T1 (TNNT1) (NM_003283) Human 3' UTR Clone

CAT#: SC201130

3' UTR clone of troponin T type 1 (skeletal slow) (TNNT1) transcript variant 1 for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

Specifications

Product Data
Product Name Troponin T1 (TNNT1) (NM_003283) Human 3' UTR Clone
Vector pMirTarget
Synonyms ANM; NEM5; STNT; TNT; TNTS
ACCN NM_003283
Insert Size 247 bp
Sequence Data
>SC201130 3’UTR clone of NM_003283
The sequence shown below is from the reference sequence of NM_003283. 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_003283.6
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
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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