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Luria-Bertani

Luria Broth Base(Miller''s LB Broth Base),粉末

Company: Thermo Fisher Scientific
Catalog#: 12795027
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Defined Mutant Library Sequencing (DML-Seq) for Identification of Conditional Essential Genes
Author:
Date:
2021-03-05
[Abstract]  

Transposon insertion sequencing (TIS) is an emerging technique which utilizes a massive transposon mutant library to screen specific phenotype and determine the conditional essential genetic requirements for bacterial fitness under distinct conditions combined with high-throughput parallel sequencing technology. Compared with a massive mutant library in traditional TIS, the defined mutant library sequencing (DML-Seq) has advantages as: 1) efficient mutagenesis; 2) low bottleneck effects; 3) avoid hotpots caused by screening; 4) can be directly used in the following experiments. Here, we described an optimized procedure of DML-Seq for fitness screen to supply classical TIS using the marine pathogenic bacterium Edwardsiella piscicida as an example.

[摘要]  [摘要]转座子插入测序(TIS)是一项新兴技术,它利用大量的转座子突变体文库筛选特定表型,并结合高通量并行测序技术,在不同条件下确定细菌适应性的条件性基本遗传要求。与传统TIS中的大规模突变文库相比,已定义的突变文库测序(DML-Seq)具有以下优势:1)高效诱变;2)瓶颈效应低;3)避免因筛选引起的火锅;4)可直接用于以下实验。在这里,我们描述DML-SEQ的优化过程进行健身屏幕使用海洋致病菌提供古典TIS爱德华piscicida作为一个例子。


[背景]转座子插入诱变与下一代测序(NGS)结合已被证明是在多种条件下研究基因功能的有效方法(Chao等,2016; Price等,2018)。通常,TIS分析由转座子插入位点的大规模平行测序和大量插入事件的统计分析组成。

基于TIS的筛选可以在多种条件下基于高度饱和的转座子突变体文库的细菌适应性,提供单个基因座和域的适应性贡献的高分辨率图(Chao等,2016)。每个位点的插入频率或相应突变体的相对丰度通常与施加选择性压力(例如宿主和抗生素施加的压力)后与基因座对适应性的贡献成反比(Chao等人,2016)。这种方法的原理是多种相关方法的基础,包括TIS,转座子测序(TnSeq ),插入测序(INSeq ),转座子定向插入位点测序(TraDIS ...

RNA ImmunoGenic Assay: A Method to Detect Immunogenicity of in vitro Transcribed mRNA in Human Whole Blood
Author:
Date:
2020-12-20
[Abstract]  The mRNA therapeutics is a new class of medicine to treat many various diseases. However, in vitro transcribed (IVT) mRNA triggers immune responses due to recognition by human endosomal and cytoplasmic RNA sensors, but incorporation of modified nucleosides have been shown to reduce such responses. Therefore, an assay signifying important aspects of the human immune system is still required. Here, we present a simple ex vivo method called ‘RNA ImmunoGenic Assay’ to measure immunogenicity of IVT-mRNAs in human whole blood. Chemically modified and unmodified mRNA are complexed with a transfection reagent (TransIT), and co-incubated in human whole blood. Specific cytokines are measured (TNF-α, INF-α, INF-γ, IL-6 and IL-12p70) using ELISAs. The ... [摘要]  [摘要] mRNA疗法是治疗多种疾病的新型药物。然而,我Ñ体外转录(IVT)的mRNA触发由于人类内体和细胞质RNA传感器,但是修饰的核苷的掺入识别的免疫应答已经示出吨ö减少此类反应。牛逼herefore ,测定标志着重要的环节人体免疫系统仍然需要。这里,我们提出一个简单的离体称为“RNA方法免疫ģ ENIC测定”测量的IVT-mRNA的免疫原性小号在人全血。将化学修饰和未修饰的mRNA与转染试剂(TransIT )复合,并在人全血中共同孵育。特异性细胞因子测定(TNF- α ,INF- α ,INF- γ ,IL-6和IL-12p70的),使用的ELISA。进行qPCR分析以揭示特异性免疫途径的激活。所述RNA免疫ģ ENIC测定提供小号的简单且快速的方法来检测供体特异性-针对mRNA的治疗剂的免疫应答。

图形摘要:

RNA免疫基因测定的示意图

[背景] mRNA治疗是基因治疗的重要一类(Sahin等,2014 ;Antony等,2015 ...

Dense sgRNA Library Construction Using a Molecular Chipper Approach
Author:
Date:
2017-06-20
[Abstract]  Genetic screens using single-guide-RNA (sgRNA) libraries and CRISPR technology have been powerful to identify genetic regulators for both coding and noncoding regions of the genome. Interrogating functional elements in noncoding regions requires sgRNA libraries that are densely covering, and ideally inexpensive, easy to implement and flexible for customization. We present a Molecular Chipper protocol for generating dense sgRNA libraries from genomic regions of interest. This approach utilizes a combination of random fragmentation and a Type III restriction enzyme to derive a dense coverage of sgRNA library from input DNA. [摘要]  使用单导向RNA(sgRNA)文库和CRISPR技术的遗传筛选功能强大可以识别基因组编码区和非编码区的遗传调控因子。 在非编码区域中询问功能元件需要密集覆盖的sgRNA文库,理想的便宜,易于实现和灵活定制。 我们提出了一个分子切片方案从感兴趣的基因组区域产生密集的sgRNA文库。 该方法利用随机断裂和III型限制酶的组合从输入DNA导出sgRNA文库的致密覆盖。
【背景】使用化脓性链球菌(sp)的基因组编辑Cas9和sgRNA文库是通过产生双重缺失功能序列改变来筛选哺乳动物细胞功能性遗传调节因子的有力工具(Wiedenheft et al。,2012; Mali et al。,2013; Koike-Yusa等,2014; Shalem等,2014; Wang等,2014; Zhou等,2014)。 Cas9结合sgRNA,其可被设计为将Cas9靶向基因组中定义的基因座。 Cas9的核酸酶活性切割靶DNA位点,导致双链DNA断裂,在通过非同源末端连接途径进行DNA修复时,经常导致感兴趣的基因座短缺失。
CRISPR-Cas9系统强大的基因组编辑能力导致使用sgRNA文库来询问蛋白质编码基因以及非编码区域。通过sgRNA富集功能筛选,报告了几种用于蛋白质编码基因和/或有限数量的非编码基因的sgRNA文库,以鉴定调控特定细胞功能的基因和网络(Koike-Yusa等,2014; ...

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