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ddTTP [2',3'-Dideoxythymidine-5'-triphosphate] *10 mM in ddH2O*

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Physical properties
Molecular weight466.17
SolventWater
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12171501

OverviewpdfSDSpdfProtocol


Molecular weight
466.17
Sanger sequencing, also known as the chain termination method, is a technique for DNA sequencing based upon the selective incorporation of chain-terminating dideoxynucleotides (ddNTPs) by DNA polymerase. It was developed by Frederick Sanger and colleagues in 1977. Although the newer NGS technologies are becoming common in clinical research labs due to their higher throughput capabilities and lower costs per sample, Sanger sequencing with 99.99% accuracy is still the “gold standard” for clinical research sequencing. dd-TTP is one of the four critical ddNTP components for performing Sanger sequencing.

Calculators


Common stock solution preparation

Table 1. Volume of Water needed to reconstitute specific mass of ddTTP [2',3'-Dideoxythymidine-5'-triphosphate] *10 mM in ddH2O* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM214.514 µL1.073 mL2.145 mL10.726 mL21.451 mL
5 mM42.903 µL214.514 µL429.028 µL2.145 mL4.29 mL
10 mM21.451 µL107.257 µL214.514 µL1.073 mL2.145 mL

Molarity calculator

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References


View all 10 references: Citation Explorer
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Authors: Di Giusto, Daniel A and King, Garry C
Journal: Nucleic acids research (2004): e32
Detection and genotyping of human papillomavirus DNA in cervical cancer tissues with fluorescence polarization.
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Journal: Sheng wu hua xue yu sheng wu wu li xue bao Acta biochimica et biophysica Sinica (2003): 1029-34
Dye structure affects Taq DNA polymerase terminator selectivity.
Authors: Brandis, J W
Journal: Nucleic acids research (1999): 1912-8
Synergistic inhibition of HIV-1 reverse transcriptase by combinations of chain-terminating nucleotides.
Authors: Villahermosa, M L and Martinez-Irujo, J J and Cabodevilla, F and Santiago, E
Journal: Biochemistry (1997): 13223-31
Characterization of the p68/p58 heterodimer of human immunodeficiency virus type 2 reverse transcriptase.
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Journal: Biochemistry (1996): 1911-7
Mechanism of inhibition of DNA synthesis by 1-beta-D-arabinofuranosyl-E-5-(2-bromovinyl)uracil.
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Journal: Microbiology and immunology (1993): 511-3
Wheat embryo DNA polymerase A reverse transcribes natural and synthetic RNA templates. Biochemical characterization and comparison with animal DNA polymerase gamma and retroviral reverse transcriptase.
Authors: Laquel, P and Sallafranque-Andreola, M and Tarrago-Litvak, L and Castroviejo, M and Litvak, S
Journal: Biochimica et biophysica acta (1990): 139-48
Expression of enzymatically active reverse transcriptase of simian immunodeficiency virus in bacteria: sensitivity to nucleotide analogue inhibitors.
Authors: Prasad, V R and Myrick, K and Haseltine, W and Goff, S P
Journal: Virology (1990): 896-900
3'-Deoxy-3'-fluorothymidinetriphosphate: inhibitor and terminator of DNA synthesis catalysed by DNA polymerase beta, terminal deoxynucleotidyl transferase and DNA polymerase I.
Authors: Matthes, E and Lehmann, C and Drescher, B and Büttner, W and Langen, P
Journal: Biomedica biochimica acta (1985): K63-73
A fidelity assay using "dideoxy" DNA sequencing: a measurement of sequence dependence and frequency of forming 5-bromouracil X guanine base mispairs.
Authors: Lasken, R S and Goodman, M F
Journal: Proceedings of the National Academy of Sciences of the United States of America (1985): 1301-5