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Key Documents

MSANGERV

Sigma-Aldrich

桑格全基因组 慢病毒 CRISPR 文库

Mouse, Virus Format

同義詞:

Arrayed CRISPR library, Sanger CRISPR library

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About This Item

分類程式碼代碼:
41105904

品質等級

包裝

pkg of 10 μL (384-well plate)

濃度

1x106  VP/ml (via p24 assay)

應用

CRISPR

運輸包裝

dry ice

儲存溫度

−70°C

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一般說明

两名基因组编辑领导者Sigma-Aldrich和Wellcome Trust Sanger Institute联手打造了第一个阵列化的慢病毒CRISPR基因敲除文库。基于文献中已验证的技术,Sanger CRISPR库将使您的实验室走在竞争的最前沿,以实现下一个重大发现。

應用

功能基因组学/筛选/靶标验证

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 mouse 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

包裝

384 well plates

成分

Lentivirus Transduction Particles of gRNA-only lenti-based vectors. 2 knockout clones for every human protein-coding gene. Nearly 40,000 sequence confirmed clones


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外觀

10μl of lentivirus at ≥106 particles/ml in ~120×384 well plates

其他說明

This product is for R&D use only, not for drug, household, or other uses. Lentivirus manufacturing is achieved by using 2nd generation packaging plasmids on a 3rd generation lenti-based vector. Though the lentiviral transduction particles produced are replication incompetent, it is recommended that they be treated as Risk Group Level 2 (RGL-2) organisms in laboratory handling. Follow all published RGL-2 guidelines for laboratory handling and waste decontamination.

推薦產品

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Enhancing the genome editing toolbox: genome wide CRISPR arrayed libraries.
Metzakopian, E. et al
Scientific Reports, 7 (2017)

文章

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。

Genome-wide screening with optimized gRNAs per gene ensures specific and efficient knockout, controlling time and cost.

Get tips for handling lentiviruses, optimizing experiment setup, titering lentivirus particles, and selecting helpful products for transduction.

獲得處理慢病毒、優化實驗設定、滴定慢病毒粒子以及選擇有用的轉導產品的技巧。

條款

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.

瞭解 Sanger 測序步驟或鏈終止法,以及 DNA 測序的工作原理和如何準確讀取 Sanger 測序結果以進行研究。

FACS sorts cells based on light scattering and fluorescence for objective cell analysis.

FACS 根據光散射和螢光來分類細胞,以進行客觀的細胞分析。

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

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