快速質(zhì)粒DNA小量試劑盒

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8分鐘內(nèi)分離純化最多達(dá)30 μg分子生物學(xué)純度級(jí)別的質(zhì)粒DNA

·8分鐘內(nèi)即可完成質(zhì)粒DNA的制備，無須酚氯仿抽提

·革命性的創(chuàng)新發(fā)明Buffer N8，2分鐘內(nèi)獲得無漂浮沉淀的上清液

·核酸純化柱無須平衡液處理即可使用

·特殊的添加中和指示劑設(shè)計(jì)，使初次使用者也可以獲得最佳的質(zhì)粒抽提效果

產(chǎn)品介紹操作視頻常見問題論文引用應(yīng)用案例在線咨詢

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

快速質(zhì)粒DNA小量試劑盒

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.