Hieff Mut™ Multi Site-Directed Mutagenesis Kit 是基于Hieff Clone® 快速克隆技术的定点突变系统。使用本试剂盒,可一次性向目标质粒上三至五个不连续位点(相距超过50bp)同时引入定点突变。该试剂盒由两个模块组成:Hieff® II Pfu DNA Polymerase扩增模块和Hieff Clone® 快速克隆模块。Hieff® II Pfu DNA Polymerase超高的保真度显著降低了扩增过程中引入新突变的可能性,其卓越的长片段扩增能力,广泛适用于长度小于20 kb的任何质粒扩增。Hieff Clone®快速克隆系统利用高效的同源重组反应替代传统的退火成环反应。因此使用Hieff Mut™ Multi Site-Directed Mutagenesis Kit进行DNA定点突变时,引物设计更加灵活,且扩增反应以指数方式进行,极大减少了模板使用量,有利于原始甲基化模板的彻底降解。
Hieff Mut™ Multi Site-Directed Mutagenesis Kit中的重组酶Exnase MultiS经过优化,专门针对多碱基进行定点突变。此外,如扩增产物特异,其DpnI消化产物可不进行DNA纯化而直接用于重组反应。高度优化的反应缓冲液、快捷的操作流程以及极高的成功率,使得Hieff Mut™ Multi Site-Directed Mutagenesis Kit成为DNA多点突变试剂盒。
- 专门针对多碱基进行定点突变
- 不连续多碱基(相距超过50bp)定点突变实验流程(以不连续三碱基为例)
冰袋(wet ice)运输。产品-20℃保存。有效期1年。
Q:多点突变试剂盒与定点突变试剂盒有什么区别?
A:多点突变试剂盒可一步实现目标质粒上 3-5 个不连续位点的定点突变,而定点突变试剂盒是
适合 1 或 2 个不连续位点的定点突变。
如:3 个连续的碱基突变算 1 个位点的突变,故定点突
变试剂盒即可(相距超过 50 bp 为 1 个不连续位点)。
Q:点突变为什么要选择甲基化的载体?
A:点突变过程需要去除模板质粒,防止假阳性。利用的原理就是限制性内切酶DpnI 能消化甲基化的模板,若是非甲基化,则无法去除模板。
Q:对于 PCR 模板质粒什么要求?
A:a)PCR 模板应为甲基化质粒,应使用甲基化酶无缺陷型的宿主菌扩增原始质粒(如DH5α, TOP10,JM109 等)。
b)应尽量使用新鲜制备的质粒作为模板,因长期放置,反复冻融可能会导致模板质粒断裂, 开环或降解。
Q:质粒反向扩增时引物如何设计?
A:正反向扩增引物 5’端包含至少 20 bp 反向互补区域,各引物非互补区域长度至少为 20 bp。互补区尽量选择无重复序列,GC 含量尽量在 40%-60%范围内。
[1] Luo P, Xu Z, Li G, et al. HMGB1 represses the anti-cancer activity of sunitinib by governing TP53 autophagic degradation via its nucleus-to-cytoplasm transport. Autophagy. 2018;14(12):2155-2170. doi:10.1080/15548627.2018.1501134(IF:11.100)
[2] Wu R, Chen Y, Liu Y, et al. m6A methylation promotes white-to-beige fat transition by facilitating Hif1a translation. EMBO Rep. 2021;22(11):e52348. doi:10.15252/embr.202052348(IF:8.807)
[3] Ren X, Zhao H, Shi L, et al. Phosphorylation of Yun is required for stem cell proliferation and tumorigenesis. Cell Prolif. 2022;55(5):e13230. doi:10.1111/cpr.13230(IF:6.831)
[4] Wang M, Liu H, Zhang X, et al. Lack of MOF Decreases Susceptibility to Hypoxia and Promotes Multidrug Resistance in Hepatocellular Carcinoma via HIF-1α. Front Cell Dev Biol. 2021;9:718707. Published 2021 Sep 1. doi:10.3389/fcell.2021.718707(IF:6.684)
[5] Mo C, Li W, Jia K, Liu W, Yi M. Proper Balance of Small GTPase rab10 Is Critical for PGC Migration in Zebrafish. Int J Mol Sci. 2021;22(21):11962. Published 2021 Nov 4. doi:10.3390/ijms222111962(IF:5.924)
[6] Yao Y, Qu D, Jing X, et al. Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations. Front Pharmacol. 2022;12:775328. Published 2022 Jan 13. doi:10.3389/fphar.2021.775328(IF:5.811)
[7] Wang Q, Ren D, Bi Y, et al. Association and functional study between ADIPOQ and metabolic syndrome in elderly Chinese Han population. Aging (Albany NY). 2020;12(24):25819-25827. doi:10.18632/aging.104203(IF:4.831)
[8] Zhang S, Zhang Z, Shen Y, et al. SCN9A Epileptic Encephalopathy Mutations Display a Gain-of-function Phenotype and Distinct Sensitivity to Oxcarbazepine. Neurosci Bull. 2020;36(1):11-24. doi:10.1007/s12264-019-00413-5(IF:4.246)
[9] Jin X, Yu W, Ye P. MiR-125b enhances doxorubicin-induced cardiotoxicity by suppressing the nucleus-cytoplasmic translocation of YAP via targeting STARD13. Environ Toxicol. 2022;37(4):730-740. doi:10.1002/tox.23438(IF:4.119)
[10] Jin Y, Liu W, Xiang Y, et al. Maternal miR-202-5p is required for zebrafish primordial germ cell migration by protecting small GTPase Cdc42. J Mol Cell Biol. 2020;12(7):530-542. doi:10.1093/jmcb/mjz103(IF:4.000)
[11] Deng L, Gong K, Wang G. Hsa_circ_0008344 Promotes Glioma Tumor Progression and Angiogenesis Presumably by Regulating miR-638/SZRD1 Pathway. Neurotox Res. 2022;40(3):825-836. doi:10.1007/s12640-022-00504-8(IF:3.911)
[12] Liu W, Xiang Y, Zhang W, Jia P, Yi M, Jia K. Expression pattern, antiviral role and regulation analysis of interferon-stimulated gene 15 in black seabream, Acanthopagrus schlegelii. Fish Shellfish Immunol. 2018;82:60-67. doi:10.1016/j.fsi.2018.07.041(IF:3.185)
[13] Yang M, Zhu L, Zhu L, Xu D, Yuan Y. Role of a Rare Variant in APC Gene Promoter 1B Region in Classic Familial Adenomatous Polyposis. Digestion. 2021;102(4):527-533. doi:10.1159/000509234(IF:2.692)
[14] Shen L, Ji C, Lin J, Yang H. Regulation of circADAMTS6-miR-324-5p-PIK3R3 ceRNA pathway may be a novel mechanism of IL-1β-induced osteoarthritic chondrocytes. J Bone Miner Metab. 2022;40(3):389-401. doi:10.1007/s00774-021-01308-0(IF:2.626)