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| 产品优势： | • 病毒产量高 • 对于很长的 DNA（长达 180 kb）同样有效 • 同样适用于悬浮293细胞（例如293F、293H等） • H高水平的重组蛋白产量 • 血清和抗生素的存在提高了 293 细胞的效率 • 单DNA转染和多DNA共转染均具有卓越的效率 |
| 描述： |
利用我们创新的专有脂质缀合技术，LiFect293™ 转染试剂经过专门设计和配制，添加了专有的增强剂，用于转染 HEK293 细胞和其他哺乳动物细胞。 作为第二代基于脂质体的DNA转染试剂，该试剂为HEK293相关细胞以及许多哺乳动物细胞提供极高的转染效率，且细胞毒性较小。 该试剂在之前版本的基础上进行了升级，化学成分更加精细，基因传递效率提高了3~4倍。 1.0 ml 试剂足以在 24 孔板中进行约 666 次转染，或在 6 孔板中进行约 333 次转染。 |
| 组分： |
1. LiFect293™ Transfection Reagent: 1 ml |
| 储存条件： |
Store at 4°C. If stored properly, the product is stable for 12 months or longer. |
| 文档： |
General Protocol Protocol for Suspension 293 and CHO Cells Protocol for Lentivirus Production Protocol for rAAV Production |
成功案例
Comparison of transfection efficiency of LiFect293™ Transfection Reagent vs. lipofectamine 2000 (L2K) and Fugene HD on HepG2 cells.
Right Panel: Comparison of transfection efficiency of LiFect293 with Lipofecatmine 2000 (L2K), and Fugene HD on HepG2 cells. GFP DNA (pEGFP-N3) was transfected with different transfection reagents per manufacturer's protocols to HepG2 cell (cultured on Collagen pretreated dishes). GFP positive cell (%) and fluorescence intensity were detected by passing through FACS 48 hours post transfection.
Left Panel: presence of serum and antibiotics enhances LiFect293 efficiency on HepG2 cells. HepG2 cell (grown on collagen treated dishes) was transfected with three different conditions------serum and antibiotics free, presence of 10% serum and antibiotics followed by removal 5 hours post transfection and presence of 10% serum and antibiotics without removal 5 hours post transfection.
Comparison of transfection efficiency of LiFect293™ Transfection Reagent vs. lipofectamine 2000 (L2K), TransIT and Fugene 6 on CHO cells.
Right Panel: Comparison of transfection efficiency of LiFect293 Comparison of transfection efficiency of LiFect293™ reagent vs. lipofectamine 2000 (L2K), TransIT and Fugene 6 on CHO cells. ith Lipofecatmine 2000 (L2K), TransIT and Fugene 6 on CHO cells. DNAs encoding Renilla luciferase (phRL-CMV) and GFP (pEGFP-N3) were transfected with different DNA transfection reagent per manufacturer's protocols. Renilla luciferase activity and GFP fluorescence were detected with Renilla Assay System and a Nikon Eclipse fluorescent microcopy respectively 24 hours post transfection.
Left Panel: Comparison of price ($/1.0 ml vial) of LiFect293 versus those of Lipofecatmine 2000 (L2K), TransIT and Fugene 6. All the prices were collected from the manufacturers' websites.
A comparison of transfection efficiency of LiFect293™ reagent with lipofectamine 2000 (L2K) on a hard-to-transfect cell, primary rat aortic smooth muscle cells.
The rat aortic smooth muscle cells were prepared and transfected with pEGFP-N3 by LiFect293™ reagent (left panel) and Lipofecatmine 2000 (L2K, right panel) respectively per manufacturers' protocols. The transfection efficiency was evaluated by detecting GFP fluorescence with a Nikon Eclipse 2000 microscopy 24 hours post transfection.
A comparison of transfection efficiency of LiFect293™ reagent with Fugene HD on hard-to-transfect cell, LNCap cells.
The LNCap cells were grown as ATCC recommended procedures and co-transfected with pBabe-hygro-SSeCKs (1.5 µg) and pEGFP-N3 (0.5 µg) per well (6 well plate) LiFect293™ reagent (left panel) and Fugene HD (right panel) respectively per manufacturers' protocols. The transfection efficiency was evaluated by detecting GFP fluorescence with a Nikon Eclipse 2000 microscopy 24 hours post transfection.
Two examples showing exceptional efficiency of LiFect293™ reagent on hard-to-transfect cells like HepG2 and SaoS-2 cells.
HepG2 and SaoS-2 cells in 95% confluency were transfected with pEGFP-N3 and pSV-galactosidase DNAs respectively in presence of serum/antibiotics. The efficiency was checked 48 hours post transfection by Zeiss 510 Confocal Microscopy and -galactosidase staining kit respectively
A comparison of transfection efficiency of LiFect293™ reagent with 293fectin on HEK293 cells.
HEK293 cells transfected with pEGFP-C1 plasmid using LiFect293™ In Vitro DNA Transfection Reagent (upper panel) and the most popular brand product 293fectin of Invitrogen (lower panel). The cells were visualized by Nikon Eclipse Fluorescence microscope with DIC phase imaging (left panel) and FITC imaging (right panel) 24 hours post-transfection.
A comparison of LiFect293™ reagent vs. 293fectin, Xfect and Fugene 6 transfection reagents on protein production with suspension 293F cells.
30 ml of 293F cell cultured in standard culture medium was transfected with pEGFP-6x His plasmid using LiFect293™ Transfection Reagent (20 µg plasmid DNA), 293Fectin (30 µg plasmid DNA), Xfect (30 µg plasmid DNA) and Fugene 6 (30 µg plasmid DNA) per manufacturers' standard transfection protocols. GFP fluorescence was visualized 48 hours post transfection (left panel) with A for LiFect293, B for 293fectin, C for Xfect and D for Fugene 6. The 6x His tagged GFP protein was then purified via Ni-NTA affinity column. 5 µl of 1st elution fraction was resolved on SDS-PAGE followed by Coomassie Brilliant Blue staining (right upper panel E) with the lane 1 for LiFect293, lane 2 for protein marker, lane 3 for Xfect, lane 4 for 293fectin and lane 5 for Fugene 6. The protein yield was quantified via spectrometer (right lower panel F).
