Effectene Transfection Reagent

对原代细胞和敏感细胞系的DNA转染

S_1293_GEF_TF0408

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Effectene Transfection Reagent (1 ml)

目录编号 / ID.   301425

1 ml Effectene Reagent, Enhancer, Buffer; for 40 transfections in 60 mm dishes or 160 transfections in 12-well plates
PLN 3,317.00
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数量
1 ml
4 x 1 ml
Effectene Transfection Reagent 旨在用于分子生物学应用。该产品不能用于疾病诊断、预防和治疗。

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✓ 博学专业的产品和技术支持

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特点

  • 在血清存在的情况下进行高效转染
  • 只需使用少量DNA 即可达到高效转染
  • 高转染效率而且较低的DNA使用量
  • 适合高通量筛选

产品详情

Effectene Transfection Reagent是一种非脂质体的脂类转染剂,能将DNA转入多种类型的细胞。因其毒性低,非常适合敏感细胞如原代细胞的转染。

绩效

Effectene Transfection Reagent 的操作流程简单, 转染质粒DNA比用其他的试剂获得的转染效率高(参见" High transfection efficiencies using Effectene Reagent")。Effectene Transfection Reagent适用于带有寡核苷酸的敏感细胞系的转染(参见" Transfection of oligonucleotides using Effectene Reagent")。特别适用于原代细胞(参见" 40% transfection efficiency in primary cells")。 使用Effectene Transfection Reagent已成功转染了许多细胞系和原代细胞。有针对不同细胞类型的转染方案。细胞毒性低,因为可在血清存在的情况下使用Effectene Transfection Reagent进行转染且DNA用量低(参见" Serum and DNA quantity vs. transfection efficiency")。

DNA重组技术应用于药物研发领域,导致对高通量转染需求增加。使用Effectene Transfection Reagent进行转染DNA用量低,手动操作少。此外,无需移除转染复合物,使该试剂高度适用于高通量筛选。Effectene Transfection Reagent适用于批量转染。

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原理

Effectene Transfection Reagent是一种全新的非脂质体的脂类转染剂,将DNA 与浓缩增强子和优化的缓冲液混合使用以达到高效转染。浓缩增强子先聚合DNA分子,Effectene Transfection Reagent随后用阳离子脂质包围聚合的DNA分子。采用一种特殊有效的方法将DNA转入真核细胞。这种特性保证了复杂复合物转染的可重现性。

程序

Effectene流程分为两步。将DNA与浓缩增强子混合后,加入Effectene Transfection Reagent形成复合物,这一步只需2–5分钟。然后加入Effectene Transfection Reagent,与混合物一起反应5–10分钟以形成Effectene–DNA复合物。复合物与培养基混合(可以含有血清和抗体),直接加入到细胞中。培养细胞至成熟,分析基因表达(参见" Effectene transfection procedure")。

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应用

Effectene Transfection Reagent适用于多种类型细胞的瞬时和稳定转染。

辅助数据和图表

规格

特点规格
applicationsRNAi studies, gene expression studies, high-throughput transfections
technologyNon-liposomal lipid formulation in conjonction with a DNA-condensing enhancer
numberofpossibletransfections160 transfections in 12-well plates / 1 ml reagent
celltypeEukaryotic cells (primary cells and sensitive cells)
featuresNon-liposomal lipid formulation, minimal cytotoxicity
transfectiontypeTransient and stable transfection
controlsNot included
nucleicacidDNA

资源

补充实验方案 (7)
The following protocol is optimized for transient transfection of CHO cells in 96-well plates without pre-plating of cells 24 h prior to transfection. Cell plating and transfection are performed on the same day, making this protocol rapid and convenient.
The following protocol is optimized for transient transfection of 293 cells in 96-well plates without pre-plating of cells 24 h prior to transfection. Cell plating and transfection are performed on the same day, making this protocol rapid and convenient.
The following protocol is optimized for transient transfection of COS-7 cells in 96-well plates without pre-plating of cells 24 h prior to transfection. Cell plating and transfection are performed on the same day, making this protocol rapid and convenient.
试剂盒操作手册 (1)
The next generation in lipid technology 
产品介绍与指南 (2)
Brochure detailing reagents for efficient and robust DNA and RNA transfection.
快速启动实验方案 (1)
安全数据表 (1)
Download Safety Data Sheets for QIAGEN product components.
Certificates of Analysis (1)