找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

Titlebook: CRISPR-Cas Methods; Volume 2 M. Tofazzal Islam,Kutubuddin Ali Molla Book 2021 The Editor(s) (if applicable) and The Author(s), under exclus

[復(fù)制鏈接]
樓主: Madison
21#
發(fā)表于 2025-3-25 04:14:42 | 只看該作者
Jürgen S?keland,Angelika S?kelandbinase polymerase amplification, target gene detection with Cas12a, and lateral flow assay. Owing to its simplicity, efficiency, robustness, and low-cost, this all-paper-based Cas12a DNA test method could be easily applied in field for crop disease diagnosis and GMO test.
22#
發(fā)表于 2025-3-25 10:59:19 | 只看該作者
23#
發(fā)表于 2025-3-25 15:24:22 | 只看該作者
24#
發(fā)表于 2025-3-25 19:30:11 | 只看該作者
In Silico Analysis of gRNA Secondary Structure to Predict Its Efficacy for Plant Genome Editing, structure in target recognition and efficacy of CRISPR-Cas systems, it is vital to assess the gRNA secondary structure. Here, we describe a protocol to determine the gRNA secondary structure using RNA-fold software and explain how to interpret the results.
25#
發(fā)表于 2025-3-25 20:50:24 | 只看該作者
26#
發(fā)表于 2025-3-26 01:46:43 | 只看該作者
Targeted Base Editing in Soybean Using a CRISPR-Cas9 Cytidine Deaminase Fusion,posed of nCas9, a rat cytidine deaminase enzyme APOBEC1, and a uracil DNA glycosylase inhibitor (UGI). The CBE was constructed in the PTF101 vector background. The PTF101-CBE has successfully achieved single-base alteration in soybean. Here, we present a detailed protocol of this base editor to generate a point mutation in soybean.
27#
發(fā)表于 2025-3-26 05:05:56 | 只看該作者
Efficient CRISPR-Cas9-Mediated Genome Editing in Tomato,ovide a detailed protocol for highly efficient plant transformation and regeneration in tomato to generate stable lines along with variant analysis of putative mutant lines followed by phenotypic analysis for the trait-of-interest. From the design of target site, generation of genome-edited tomato plants can be realized in 16–20?weeks.
28#
發(fā)表于 2025-3-26 12:23:09 | 只看該作者
CRISPR-Cas12a-Based DNA Detection for Fast Pathogen Diagnosis and GMO Test in Plants,binase polymerase amplification, target gene detection with Cas12a, and lateral flow assay. Owing to its simplicity, efficiency, robustness, and low-cost, this all-paper-based Cas12a DNA test method could be easily applied in field for crop disease diagnosis and GMO test.
29#
發(fā)表于 2025-3-26 14:30:03 | 只看該作者
30#
發(fā)表于 2025-3-26 18:24:07 | 只看該作者
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點(diǎn)評 投稿經(jīng)驗(yàn)總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機(jī)版|小黑屋| 派博傳思國際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-7 21:53
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
孝义市| 太仆寺旗| 博白县| 和平县| 略阳县| 仪征市| 齐河县| 资源县| 铜梁县| 丘北县| 道孚县| 赫章县| 德庆县| 舒城县| 滦平县| 丽江市| 古丈县| 富川| 前郭尔| 郸城县| 黔西| 郑州市| 台北市| 平昌县| 周口市| 剑阁县| 柳河县| 永福县| 柯坪县| 全椒县| 绵竹市| 陵川县| 桓台县| 昭平县| 康马县| 伊吾县| 甘谷县| 都兰县| 盐池县| 德昌县| 公安县|