快速质粒DNA小量试剂盒

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8分钟内分离纯化最多达30 μg分子生物学纯度级别的质粒DNA

·8分钟内即可完成质粒DNA的制备，无须酚氯仿抽提

·革命性的创新发明Buffer N8，2分钟内获得无漂浮沉淀的上清液

·核酸纯化柱无须平衡液处理即可使用

·特殊的添加中和指示剂设计，使初次使用者也可以获得最佳的质粒抽提效果

产品介绍操作视频常见问题 COA文档应用案例在线咨询

cDNA cloning, prokaryotic expression and functional analysis of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) in Pogostemon cablin
单位：海南大学 G Zhang, Y Wu, ZUH Muhammad, Y Yang, J Yu… Protein expression and…,2019 Elsevier
An Early Diagnostic Clue for?COL18A1-?and?LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline
P Wang, X Jia, X Xiao, S Li, Y Long, M Liu…?- Frontiers in Cell and?…,?2021?- frontiersin.org
The identification of a novel splicing mutation in the DMD gene of a Chinese family
单位：华中科技大学 W Liu, X Shi, Y Li, F Qiao, Y Wu?- Clinical Case Reports,?2021?- Wiley Online Library
A Novel Mutation c. 3392G> T of COL2A1 Causes Spondyloepiphyseal Dysplasia Congenital by Affecting Pre-mRNA Splicing
单位：湖州市妇幼保健院、湖州市第一人民医院、浙江大学医学院附属女子医院 L Fan, L Ji, Y Xu, G Shen, K Tang, Z Li, S Ye…?- Frontiers in?…,?2022?- ncbi.nlm.nih.gov
Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients
Jin B, Li J, Yang Q, et al. Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients[J]. Gene, 2023, 853: 147087.
Overexpression of adrenomedullin (ADM) alleviates the senescence of human dental pulp stem cells by regulating the miR-152/CCNA2 pathway
单位：海军军医大学第一附属医院、上海交通大学医学院附属同仁医院、上海东方肝胆外科医院；上海市松江区中心医院 Dou W, Xie J, Chen J, et al. Overexpression of adrenomedullin (ADM) alleviates the senescence of human dental pulp stem cells by regulating the miR-152/CCNA2 pathway[J]. Cell Cycle, 2023, 22(5): 565-579.
A case report of familial exudative vitreoretinopathy in a Chinese Family
单位：洛阳市妇幼保健院 Wang Y, Chang Y, Chai Y, et al. A case report of familial exudative vitreoretinopathy in a Chinese Family[J]. 2024.
A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate
Yang P, Zhang W, Zeng L, et al. A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate[J]. Gene, 2024: 148767.
ZjHXK5?and?ZjHXK6?negatively regulate the sugar metabolism of?Ziziphus jujuba?Mill.
Tong P, Liao G, Lu D, et al. ZjHXK5 and ZjHXK6 negatively regulate the sugar metabolism of Ziziphus jujuba Mill[J]. Frontiers in Plant Science, 2024, 15: 1335120.
Case Report: A 3’splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child
单位：郑州大学第一附属医院、深圳雅济科技有限公司 Shi D, Li N, Fan C, et al. Case Report: A 3’splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child[J]. Frontiers in Genetics, 2025, 15: 1508922.
A novel loss-of-function SYCP2 variant causes asthenoteratozoospermia in infertile males
单位：天津市中心妇产科医院生殖医学中心、天津市中心妇产科医院、人类发育与生殖调控重点实验室 Liu C, Zhang Y, Zhao Y, et al. A novel loss-of-function SYCP2 variant causes asthenoteratozoospermia in infertile males[J]. Frontiers in Genetics, 2025, 16: 1595720.
Silent but significant: Functional elucidation of a synonymous ATP7B mutation in Wilson’s disease pedigrees
单位：湖北医药学院附属随州市中心医院、襄阳中西医结合医院 Zhang Q, Xie X, Li H, et al. Silent but significant: Functional elucidation of a synonymous ATP7B mutation in Wilson’s disease pedigrees[J]. Frontiers in Genetics, 2025, 16: 1604683.
A Novel Synonymous Variant of PAX2 in Monochorionic Diamniotic Twins With Bilateral Renal Agenesis: A Case Report and Literature Review
单位：四川大学华西第二医院、四川大学 Yao W, Xu B, Wang H, et al. A Novel Synonymous Variant of PAX2 in Monochorionic Diamniotic Twins With Bilateral Renal Agenesis: A Case Report and Literature Review[J]. Molecular Genetics & Genomic Medicine, 2025, 13(6): e70113.
Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report
单位：洛阳市妇幼保健院、洛阳市儿童保健医院 Wang Y, Chang Y, Lei H, et al. Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report[J]. BMC pediatrics, 2025, 25(1): 1-8.
Involvement of the NF‐κB pathway in multidrug resistance induced by HBx in a hepatoma cell line
单位：浙江大学医学院附属第一医院 Liu Y, Lou G, Wu W, et al.Journal of viral hepatitis, 2011, 18(10): e439-e446.
Genome-wide characterization of C2H2 zinc-finger gene family provides insight into the mechanisms and evolution of the dehydration–rehydration responses in Physcomitrium and Arabidopsis
单位：浙江农林大学 Li X, Cao X, Li J, et al.Frontiers in Plant Science, 2022, 13.
An Early Diagnostic Clue for COL18A1-and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline
单位：中山大学中山眼科中心、中山大学附属第一医院生殖医学中心 Wang P, Jia X, Xiao X, et al.Frontiers in Cell and Developmental Biology, 2021, 9: 644947.
Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy
单位：深圳儿童医院、深圳雅济科技有限公司 Y Hu, M Huang, J Wen, J Gao, W Long, Y Shen…?- Frontiers in?…,?2023?- frontiersin.org
ZjHXK5 and ZjHXK6 negatively regulate the sugar metabolism of Ziziphus jujuba Mil
单位：塔里木大学、新疆阿拉尔特色果树高效优质栽培及果品深加工技术国家、华中农业大学园艺作物种质创新与利用国家重点实验室 Tong P, Liao G, Lu D, et al Frontiers in Plant Science, 2024, 15: 1335120.

快速质粒DNA小量试剂盒

cDNA cloning, prokaryotic expression and functional analysis of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) in Pogostemon cablin

An Early Diagnostic Clue for?COL18A1-?and?LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline

The identification of a novel splicing mutation in the DMD gene of a Chinese family

A Novel Mutation c. 3392G> T of COL2A1 Causes Spondyloepiphyseal Dysplasia Congenital by Affecting Pre-mRNA Splicing

Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients

Overexpression of adrenomedullin (ADM) alleviates the senescence of human dental pulp stem cells by regulating the miR-152/CCNA2 pathway

A case report of familial exudative vitreoretinopathy in a Chinese Family

A novel splice variant in intron 10 of PEX6 is associated with Zellweger Syndrome in a Chinese neonate

ZjHXK5?and?ZjHXK6?negatively regulate the sugar metabolism of?Ziziphus jujuba?Mill.

Case Report: A 3’splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child

A novel loss-of-function SYCP2 variant causes asthenoteratozoospermia in infertile males

Silent but significant: Functional elucidation of a synonymous ATP7B mutation in Wilson’s disease pedigrees

A Novel Synonymous Variant of PAX2 in Monochorionic Diamniotic Twins With Bilateral Renal Agenesis: A Case Report and Literature Review

Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report

Involvement of the NF‐κB pathway in multidrug resistance induced by HBx in a hepatoma cell line

Genome-wide characterization of C2H2 zinc-finger gene family provides insight into the mechanisms and evolution of the dehydration–rehydration responses in Physcomitrium and Arabidopsis

An Early Diagnostic Clue for COL18A1-and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline

Case report: splicing effect of a novel heterozygous variant of the NUS1 gene in a child with epilepsy

ZjHXK5 and ZjHXK6 negatively regulate the sugar metabolism of Ziziphus jujuba Mil