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安全信息

CRISPR21V

Sigma-Aldrich

Lenti CRISPR Human HPRT1 Positive Control Transduction Particles (LV04 vector)

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UNSPSC代码:
12352200
NACRES:
NA.51

形式

liquid

质量水平

包装

vial of 200 μL

浓度

(1x106 TU/ml (via p24 titering assay))

应用

CRISPR

运输

dry ice

储存温度

−70°C

一般描述

The Lenti CRISPR Human HPRT1 Positive Control Transduction Particles (LV04 vector) product is a critical positive control to monitor transduction efficiency for lentiCRISPRs. This control is produced from the sequence-verified CRISPR lentiviral plasmid targeting human HPRT1. The protein encoded by this gene is a transferase which plays a central role in the generation of purine nucleotides. Cells with intact HPRT1 will die upon exposure to 6-TG (Product No. A4882), an antimetabolite used in the treatment of leukemias. Conversely, cells with HPRT1 knocked out will increase over time with 6-TG selection. This targets a validated HPRT1 CRISPR site, which serves as an experimental control for lenti CRISPRs. The lenti CRISPR HPRT1 positive control uses a dual-component system consisting of a U6-driven guide RNA plasmid targeting the human HPRT1 gene and hPGK-driven Puromycin and BFP expression. This control requires Cas9 be delivered by a separate vector.

Lentiviral-based particles permit efficient infection and integration of the construct into differentiated and non-dividing cells, such as neurons and dendritic cells, overcoming low transfection and integration difficulties when using these cell lines. Self-inactivating replication incompetent viral particles are produced in packaging cells (HEK293T) by co-transfection with compatible packaging and envelope plasmids.

应用

功能性基因组学研究/筛选/靶标验证

其他说明

Ampicillin and puromycin antibiotic resistance genes provide selection in bacterial or mammalian cells, respectively.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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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。

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