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一般說明
應用
特點和優勢
- Vector: U6-gRNA/PGK-Puro-2A-BFP (gRNA only)
- Simplify the workflow with puromycin selection
- Illuminate CRISPR-expressing cells with BFP
Additional Features
- Better, not bigger: Two optimized clones per gene reduces the time, cost, and scale of screening experiments
- Ready-to-screen: Clones are arrayed in a robotics-friendly 384-well format for high throughput screening
- Collaborative: Real-time, library validation continues
For detailed information on the Sanger library, click here
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 3
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This screening guide covers how to choose a cell line, a screening library, and experimental conditions as well as tips for designing and performing your experiment.
Genome-wide screening with optimized gRNAs per gene ensures specific and efficient knockout, controlling time and cost.
全基因组功能缺失筛查是发现生物过程背后的基因和途径的有效方法。现在,每个基因都可通过两个优化的 gRNA 完全敲除。通过最大限度减少克隆数量,可确保尽可能特异性的筛选,同时控制时间和成本。
获取处理慢病毒、优化实验设置、测定慢病毒颗粒滴度以及选择实用转导产品方面的贴士。
实验方案
Learn about Sanger Sequencing steps or the chain termination method and how DNA sequencing works and how to read Sanger Sequencing results accurately for your research.
FACS sorts cells based on light scattering and fluorescence for objective cell analysis.
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
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