Taq PCR Mix
1.产品介绍
预混的含有优化浓度的GenStar高纯度Taq DNA Polymerase、dNTPs、Mg2+、反应缓冲液和稳定剂等成分的2倍浓度的即用型PCR试剂。使用时只需加入DNA模板和引物,并用水补足体系至反应浓度(1×)。产品有含染料(红色)和不含染料(无色)两种选择,使用含染料的产品在 PCR 反应完成后,不需添加上样缓冲液即可直接上样进行电泳。针对丙烯酰胺凝胶检测,可选用for PAGE专用产品,背景更低。
2.产品列表
产品名称 | 货号 | 规格 | 目录价 |
2×Taq PCR StarMix with Loading Dye 2×Taq预混 PCR反应体系(含染料) | A012-01 | 1 ml | 49 |
A012-05 | 1 ml×5 | 229 | |
A012-10 | 1 ml×10 | 399 | |
A012-100 | 1 ml×100 | 3599 | |
A012-505 | 5 ml×5 | 900 | |
2×Taq PCR StarMix, Loading Dye-free 2×Taq预混 PCR反应体系(无染料) | A015-10 | 1 ml×10 | 399 |
2×Taq PCR StarMix with Loading Dye(For PAGE) | A006-01 | 1 ml | 49 |
A006-05 | 1 ml×5 | 229 | |
A006-10 | 1 ml×10 | 399 | |
A006-100 | 1 ml×100 | 3599 | |
A006-505 | 5 ml×5 | 900 | |
2×Taq PCR StarMix Loading Dye-free(For PAGE) 2×无染料Taq预混PCR反应体系(丙烯酰胺凝胶电泳检测专用) | A007-10 | 1 ml × 10 | 399 |
3.产品特点
直接上样:含染料产品PCR产物可直接上样进行凝胶电泳分析;
高度灵敏:高纯度的酶带来优良的灵敏性;
无基因组污染:扩增产物纯度高;
高效扩增:优化的缓冲体系发挥更强的扩增性能;
重复性好:体系预混合,减小加样误差,降低污染机会;
性能稳定:4℃保存3-6个月或室温(25℃)保存2-4周,反复冻融50 次,扩增性能无变化;
批次稳定:遵循标准化生产流程,经过严格的质量检测。
4.实验数据
1) 鼠尾样品扩增检测
鼠尾样品扩增检测。其中1-5为不同品牌产品,G1为GenStar A012批次1,G2为GenStar A012批次2。可见使用GenStar A012扩增不同引物条带清晰、扩增产物量高。
2) 水稻样品扩增检测
水稻样品扩增检测。其中P1-P7为不同产物大小扩增引物,可见使用GenStar A012扩增批间稳定,不同引物条带清晰、扩增产物量高。
3) 菌落PCR检测
菌落PCR扩增检测。使用产品为GenStar A012。
4) PAGE凝胶电泳
聚丙烯酰胺凝胶电泳检测。使用产品为GenStar A006。
5.引用文献
1. Weihong Xie, Shouheng Jin, Yaoxing Wu, et al. Auto-ubiquitination of NEDD4-1 Recruits USP13 to Facilitate Autophagy through Deubiquitinating VPS34. CELL REP. 2020, Doi:10.1016/j.celrep.2020.01.088. IF:8.04
2. Pan Zhang, Biliang Zhang, Jian Jiao, et al. Modulation of Symbiotic Compatibility by Rhizobial Zinc Starvation Machinery. MBIO. 2020, Doi:10.1128/mBio.03193-19. IF: 5.94
3. Lili Yue, Liuqing Wang, Yangchun Du, et al. Type 3 Inositol 1,4,5-Trisphosphate Receptor is a Crucial Regulator of Calcium Dynamics Mediated by Endoplasmic Reticulum in HEK Cells. CELLS-BASEL. 2020, Doi:10.3390/cells9020275 IF: 5.77
4. YueXu, PingZhou, SenCheng, et al. A Bacterial Effector Reveals the V-ATPase-ATG16L1 Axis that Initiates. CELL. 2019. IF: 24.38
5. Jingke Xie, Weikai Ge, Nan Li, et al. Efficient base editing for multiple genes and loci in pigs using base editors. NAT COMMUN. 2019; 10: 2852.Doi:10.1038/s41467-019-10421-8 IF: 12.19
6. Ran-Ran Xing, Ran-Ran Hu, Jian-Xun Han, et al. DNA barcoding and mini-barcoding in authenticating processed animal-derived food: A case study involving the Chinese market. FOOD CHEM. 2019. IF: 5.399
7. Xinming Shen, Wei Liu, Yongjiu Chen, et al. Diagnostic significance of metallothionein members in recognizing cadmium exposure in various organs under low-dose exposure. CHEMOSPHERE. 2019. IF: 5.108
8. Lishi Li, Yulong Song, Xinrui Shi, et al. The landscape of miRNA editing in animals and its impact on miRNA biogenesis and targeting. Genome Res. 2018. IF: 10.101
9. Yushuai Wang, Weiqi Liang, Tian Tang, Constant conflict between Gypsy LTR retrotransposons and CHH methylation within a stress‐adapted mangrove genome. New Phytologist. 2018. Doi:10.1111/nph.15209 IF: 7.433
10. Yaqin Du, Ting Wang, Jun Xu, et al. Efficient derivation of extended pluripotent stem cells from NOD-scid Il2rg?/? mice. Protein & Cell. (2018). Doi:10.1007/s13238-018-0558-z IF: 6.228
11. Weili Liu, Ting Li, Pingzhang Wang, et al. LRRC25 plays a key role in all-trans retinoic acid-induced granulocytic differentiation as a novel potential leukocyte differentiation antigen. Protein & Cell. 2018. IF: 6.228
12. M. Wang, F. Liu,P.W. Crous, and L. Cai. Phylogenetic reassessment of Nigrospora: Ubiquitous endophytes, plant and human pathogens. Persoonia. 2017. Doi:10.3767/persoonia.2017.39.06 IF: 8.182
13. Ming-Hao Hu, Shuo-Bin Chen, Bo Wang, et al. Specific targeting of telomeric multimeric G-quadruplexes by a new triaryl-substituted imidazole. Nucleic Acids Research, 2017, Doi:10.1093/nar/gkw1195 IF: 10.162
14. Jie Wang, Tao Shen, Xiangbo Huang, et al. Serum hepatitis B virus RNA is encapsidated pregenome RNA that may be associated with persistence of viral infection and rebound. Journal of Hepatology. 2016. Doi:10.1016/j.jhep.2016.05.029 IF: 12.486
15. J Liu, N Sun, M Liu, et al; An autoregulatory loop controlling Arabidopsis HsfA2 expression: role of heat shock-induced alternative splicing. Plant Physiology, 2013. IF: 6.841
更多
企业名称
北京康润诚业生物科技有限公司
企业信息已认证
企业类型
信用代码
9111011476992523XK
成立日期
2004-12-15
注册资本
1100
经营范围
PCR、qPCR、核酸纯化、DNA Marker、蛋白 Marker、快速克隆表达载体、细胞产品、蛋白产
北京康润诚业生物科技有限公司
公司地址
北京市昌平区生命园路4号院1号楼A座6层
客服电话