dNTP Mix, 100mM, Lithium Salt
Ready-to-use sequencing grade ultra-pure Deoxynucleotide triphosphate (dNTP) mix, 25 mM each of dATP, dCTP, dGTP and dTTP solution (100 mM total), supplied as lithium salts in purified water at pH 7.5, enzymatically synthesized from premium quality raw materials, using highly specific production systems in our purpose-built facilities. The manufacturing process eliminates impurities and PCR-specific inhibitors such as modified nucleotides, tetraphosphates, and pyrophosphates commonly observed in other commercially available dNTP products (>99% purity determined by quantitative HPLC). Lithium salts have greater resistance to repeated freezing and thawing cycles than sodium salts, and lithium salt dNTP preparations remain sterile over the entire shelf-life due to the bacteriostatic activity of lithium towards various microorganisms.
Highly sensitive multiplex qPCR reaction
A 10-fold serial dilution of human genomic DNA amplified with four different probes, both in singleplex reactions (blue line) and quadruplex reaction (red line) using dATP, dCTP, dGTP and dTTP in lithium salt. The results illustrate the same high sensitivity, excellent reproducibility and Ct values for both the singleplex and multiplex reactions with no reduction of efficiency often associated with multiplexing.
dNTP Mix, 100mM (Lithium), MDX051
锂盐溶液中 dATP、dGTP、dCTP 和 dTTP 的超纯混合物，由优质原料酶法合成。
文档与资源
Description
Ultra-pure dNTP (dATP (2’-Deoxyadenosine-5’-Triphosphate), dCTP (2’-Deoxycytidine-5’-Triphosphate), dGTP (2’-Deoxyguanosine-5’-Triphosphate) and dTTP (2’-Deoxythymidine-5’-Triphosphate)) lithium salt solution is enzymatically synthesized from premium quality raw materials, using highly specific production systems in our purpose-built facilities.
Specifications
| Description | Ultra-pure dNTP (dATP (2’-Deoxyadenosine-5’-Triphosphate), dCTP (2’-Deoxycytidine-5’-Triphosphate), dGTP (2’-Deoxyguanosine-5’-Triphosphate) and dTTP (2’-Deoxythymidine-5’-Triphosphate)) lithium salt solution is enzymatically synthesized from premium quality raw materials, using highly specific production systems in our purpose-built facilities. | |||
| dATP | dCTP | dGTP | dTTP | |
| Composition | C10H12N5O12P3Li4, | C10H12N3O13P3Li4 | C10H12N5O13P3Li4 | C10H13N2O14P3Li4 |
| Molecular weight | 514.916 g/mol | 490.891 g/mol | 530.916 g/mol | 505.903 g/mol |
| λmax (at pH 7.0) | 259 ± 1 nm | 272 ± 1 nm | 252 ± 1 nm | 267 ± 1 nm |
| A250/A260 | 0.78 ± 0.03 | 0.82 ± 0.03 | 1.16 ± 0.05 | 0.65 ± 0.03 |
| A280/A260 | 0.15 ± 0.02 | 0.98 ± 0.03 | 0.66 ± 0.03 | 0.73 ± 0.02 |
| Concentration
|
25 mM ± 5%
(at λmax, pH 7.0, ԑ = 15.4 E x mmol-1 x cm-1) |
25 mM ± 5%
(at λmax, pH 7.0, ԑ = 9.1 E x mmol-1 x cm-1) |
25 mM ± 5%
(at λmax, pH 7.0, ԑ = 13.7 E x mmol-1 x cm-1) |
25 mM ± 5%
(at λmax, pH 7.0, ԑ = 9.5 E x mmol-1 x cm-1) |
| Presentation | 1 vials | |||
| pH of Solution (at 20°C) | 7.5 – 8.0 | |||
| Appearance | Clear, colorless solution | |||
| Application | cDNA synthesis, PCR, long-range PCR (>20 kb), high fidelity PCR, RT-PCR, qPCR, RT-qPCR, LAMP, microarrays, long NGS | |||
| Consistency | Single band with PCR amplification of a 3 kb amplicon with a serial dilution of dNTP. | |||
| DNA contamination | None detected in qPCR amplification with traces overlay with the negative control on E. coli and mouse genomic DNA specific targets. | |||
| DNase/RNase/Nickase activity | None detected | |||
| Purity dNTP
(HPLC Area % at λmax) |
≥99% | |||
| dNDP + dNMP
(HPLC Area % at λmax) |
<1% | |||
| DNase/RNase Contamination | No detectable degradation | |||
产品资料
分子诊断的原料试剂解决方案分子诊断的原料试剂解决方案
核苷酸核苷酸
FAQs: dNTP Mix, 100mM
dNTPs or deoxynucleotide triphosphates are the “building blocks” for DNA. Purity and stability of dNTPs are two of the essential factors to achieve a successful PCR. The use of a highly purified dNTP preparation is particularly recommended for sensitive techniques such as long-range PCR, RT-PCR, multiplex PCR, mutagenesis experiments and real-time applications. The purity of dNTPs is also important when the starting amount of template is minimal.
The standard concentration of a dNTP for PCR reactions is 0.2 mM. If the starting stock is a 25 mM solution of each dNTP in a 100mM dNTP Mix, you need to add 0.5 µL to a 50 µL standard PCR reaction.
It depends. You probably can increase the DNA yield, but you will have to optimize the complete PCR reaction, adjust the buffer, the Mg2+ and so on. It is not a matter pertaining only to nucleotides.
Yes. The sodium salt dNTP products are a standard grade and so we recommend these dNTPs for PCR. For more sophisticated reactions such as amplification of long templates, real-time PCR and NGS, we recommend lithium salt dNTP products.
Yes. The optimal pH for storage of nucleotides is from pH 7.0-8.2 (pH at 20°C). An acidic pH will cause hydrolysis of dATPs (deoxyadenosine triphosphate) to dADPs (deoxyadenosine diphosphates) and dAMPs (deoxyadenosine monophosphates), rendering them less suitable for PCR applications. During freezing/thawing cycles, the pH of the dATP solution can differ from the pH at 20°C. Sodium salts are temperature sensitive, so care needs to be taken when repeatedly frozen and thawed and sodium salt dATP is better aliquoted into smaller volumes and kept frozen in order to extend their shelf life.
dNTPs的酶法合成使用高度特异性的酶法系统，消除杂质和PCR抑制剂，如修饰的核苷酸、PPi和脱氧核苷四磷酸。 化学生产过程中产生的污染物，如痕量的dNDPs、焦磷酸盐或其他离子物种(如醋酸盐)，阻碍了PCR反应。 这种污染可能导致低产量或根本没有扩增产物。 除非彻底纯化，否则化学合成的dNTPs通常含有四磷酸脱氧核苷，这是强有力的PCR抑制剂。 化学合成也可以导致脱氨和其他核苷酸修饰，而酶法合成dNTPs可以绕过这些风险。
The concentration of our dNTP Mix are total – 100 mM dNTP Mix is made up of 25 mM of each dNTP (dATP, dCTP, dGTP and dTTP).
We recommend that you dilute your dNTPs using molecular biology or PCR grade water.
Yes, all of our dNTPs are glycerol-free and so can be lyophilized.
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