目录号：EN-1

稳定性

             所有的dNTPs都非常稳定，我们保证自购买之日起一年内100%稳定。

特点

             超纯度: >99% by HPLC

             可靠：混合保证和单包装的重复性都非常好。

应用

             PCR 和定量PCR

             cDNA合成

             引物合成

             DNA测序

             DNA标记

             突变基因

质控标准

            纯度检测(HPLC) >99%

            无焦磷酸盐、DNA、RNA、DNase、RNase和DNA切口

            通过操作PCR, 定量PCR和RT-PCR 检测

精选引用

想了解使用我们的dNTP已发表的研究文献吗？

Visualized RNA detection of SARS-CoV-2 in a closed tube by coupling RT-PCR with nested invasive reaction

^{_{Analyst    |    4 Jan 2023    |    DOI: https://doi.org/10.1039/d2an01679f}}

^{_{The 20 μL reaction mixtures of the assay contained 1× visualized closed-tube PCR buffer (10 mM Tris–HCl (pH 8.5), 7.5 mM MgCl2·6H2O, 30 mM NaCl, 0.05% NP-40, 0.05% Tween-20), 50 U HiScript II reverse transcriptase, 0.25 mM dNTPs (SBS Genetech Co. Ltd, Beijing, China), 0.5 μM forward primer, 0.5 μM reverse primer, 0.25 U GoTaq DNA polymerase (Promega, Beijing, China), 3.5% PEG8000 (BSK Technology Co. Ltd, Nanjing, China), 0.1 μM UP, 0.4 μM DP, 0.2 μM hairpin probe, 100 ng of FEN1 endonuclease (prepared in our laboratory.}}

CRISPR/Cas genome editing perspectives for barley breeding

^{_{Psysiologia Plantarum    |    22 Apr 2022    |    DOI: https://doi.org/10.1111/ppl.13686}}

^{_{Primers for sgRNA of eIF4E genes were selected with WhU6 promoter region for amplification of a 362-base pair fragment: F 5′-GACCAAGCCCGTTATTCTGAC-3′, R 5′-AAGTCTGATGCAGCAAGCGAG-3′; for the region including Cas9 with the promoter: F 5′-GCTCCTGGTCCATCCACG-3′, R 5′-CGTG-GATGGACCAGGAGC-3′; for hptII: F 5′-GCTGCGCCGATGGTTTCTACA-3′, R 5′-GCCCAAAGCATCAGCTCATCG. The recommended amplification mixture contained 5 mg of the DNA template (Applied Biosystems); 2.5 mM MgCl2; 250 μM dNTPs (Beijing SBS Genetech Co., Ltd.)}}

Femtomolar and locus-specific detection of N6-methyladenine in DNA by integrating double-hindered replication and nucleic acid-functionalized MB@Zr-MOF

^{_{Journal of Nanobiotechnology    |    7 Dec 2021    |    DOI: https://doi.org/10.1186/s12951-021-01156-0}}

^{_{Klenow Fragment DNA polymerase (3′ → 5′ exo−), 10 ×  Klenow buffer (500 mM Tris–HCl, 50 mM MgCl2 and 10 mM DTT, pH 7.9), and 10 × CutSmart™ buffer (20 mM Tris–acetate, 500 mM potassium acetate, 10 mM magnesium acetate and 100 µg/mL BSA, pH 7.9) were obtained from New England Biolabs (Beijing, China). GoldView I, 20 bp DNA marker, and dATPs, dTTPs, dCTPs and dGTPs were purchased from SBS Genetech Co., Ltd., (Beijing, China)}}

Multiplex Visualized Closed-Tube PCR with Hamming Distance 2 Code for 15 HPV Subtype Typing

^{_{Anal. Chem.    |    22 Mar 2021    |    DOI: https://doi.org/10.1021/acs.analchem.1c00035}}

^{_{Reagents included GoTaq Hot Start Polymerase (Taq DNA polymerase) (Promega), flap endonuclease 1 (FEN1) prepared in our laboratory as described previously, (19) deoxynucleotide triphosphates (dNTPs) (SBS Genetech Co., Ltd., China)}}

An integrated electrochemical biosensor based on target-triggered strand displacement amplification and “four-way” DNA junction towards ultrasensitive detection of PIK3CA gene mutation

^{_{Biosensors and Bioelectronics    |    15 Feb 2020    |    DOI: https://doi.org/10.1016/j.bios.2019.111954}}

^{_{NsbI restriction enzyme, Klenow Fragment (KF) (3′→5′exo-), Nb.BbvCI, 10 × Klenow buffer (500 mM Tris-HCl, 50 mM MgCl2 and 10 mM DTT, pH 7.9) and 10 × CutSmart™ buffer (20 mM Tris-acetate, 500 mM potassium acetate, 10 mM magnesium acetate and 100 μg/mL BSA, pH 7.9) were obtained from New England Biolabs (Beijing, China). GoldViewⅠ, DNA marker and dNTP were purchased from SBS Genetech Co., Ltd (Beijing, China)}}

Sequence-encoded quantitative invader assay enables highly sensitive hepatitis B virus DNA quantification in a single tube without the use of a calibration curve

^{_{Royal Society of Chemistry    |    8 Aug 2019    |    DOI: https://doi.org/10.1039/c9an00970a}}

^{_{A virus RNA/DNA Extraction Kit was purchased from Xi'an Tianlong Science and Technology Co., Ltd (Xi'an, China), deoxynucleotide triphosphates (dNTPs) were obtained from SBS Genetech Co., Ltd (Beijing, China)}}

Dual cycle amplification and dual signal enhancement assisted sensitive SERS assay of MicroRNA

^{_{Analytical Biochemistry    |    1 Jan 2019    |    DOI: https://doi.org/10.1016/j.ab.2018.10.004}}

^{_{Klenow fragment of E.coli DNA polymerase and nicking endonuclease (NEase) were purchased from Thermo Fisher Scientific Inc. (Waltham, MA, USA). BEAS-2B cells was purchased from GeFan Biotechnology.Go.,Ltd (Shanghai, China). Cell lysis buffer was purchased from Sangon Biotech (Shanghai, China). The mixture of four dNTPs (10 mM for each component) was purchased from SBS Genetech Co., Ltd. (Beijing, China).}}