|Key Features:||1. Exceptional high titers of virus production
2. Equally good for very long DNAs (up to 180 kb)
3. Equally good for suspension 293 cells (e.g., 293F, 293H, etc)
4. High levels of recombinant protein production
5. Presence of serum and antibiotics enhances efficiency on 293 cells
6. Exceptional efficiency for both single DNA transfection and multi DNAs co-transfection
||By utilizing our innovative and proprietary lipid conjugation technology, LiFect293TM Transfection Reagent is specially designed and formulated by adding proprietary enhancers for transfecting HEK293 cells and other mammalian cells. As a 2nd generation liposome based DNA transfection reagent, the reagent offers extremely high transfection efficiencies for HEK293 related cells as well as many mammalian cells with less cytotoxicity. The reagent, upgraded from its previous version with refined chemistry, is 3~4 times more efficient in gene delivery. The reagent , 1.0 ml, is sufficient for ~666 transfections in 24 well plates or ~333 transfections in 6 well plates.
||Store at 4°C. If stored properly, the product is stable for 12 months or longer.
||LiFect293TM Transfection Reagents (Free Sample)
LiFect293TM Transfection Reagents (5 ml, $889)
Protocol for Suspension 293 and CHO Cells
Protocol for Lentivirus Production
Protocol for rAAV Production
Comparisons of Transfection Efficiency of LiFectD293TM Transfection Reagent with Brand Name Products
Comparison of transfection efficiency of LiFect293TM Transfection Reagent vs. lipofectamine 2000 (L2K) and Fugene HD on HepG2 cells.
Right Panel: Comparison of transfection efficiency of LiFect293 with Lipofecatmine 2000 (L2K), and Fugene HD on HepG2 cells. GFP DNA (pEGFP-N3) was transfected with different transfection reagents per manufacturer's protocols to HepG2 cell (cultured on Collagen pretreated dishes). GFP positive cell (%) and fluorescence intensity were detected by passing through FACS 48 hours post transfection.
Left Panel: presence of serum and antibiotics enhances LiFect293 efficiency on HepG2 cells. HepG2 cell (grown on collagen treated dishes) was transfected with three different conditions------serum and antibiotics free, presence of 10% serum and antibiotics followed by removal 5 hours post transfection and presence of 10% serum and antibiotics without removal 5 hours post transfection.
Comparison of transfection efficiency of LiFect293TM Transfection Reagent vs. lipofectamine 2000 (L2K), TransIT and Fugene 6 on CHO cells.
Right Panel: Comparison of transfection efficiency of LiFect293 Comparison of transfection efficiency of LiFect293™ reagent vs. lipofectamine 2000 (L2K), TransIT and Fugene 6 on CHO cells. ith Lipofecatmine 2000 (L2K), TransIT and Fugene 6 on CHO cells. DNAs encoding Renilla luciferase (phRL-CMV) and GFP (pEGFP-N3) were transfected with different DNA transfection reagent per manufacturer's protocols. Renilla luciferase activity and GFP fluorescence were detected with Renilla Assay System and a Nikon Eclipse fluorescent microcopy respectively 24 hours post transfection.
Left Panel: Comparison of price ($/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 LiFect293TM 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 LiFect293TM 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 LiFect293TM 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) LiFect293TM 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 LiFect293TM 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 LiFect293TM reagent with 293fectin on HEK293 cells.
HEK293 cells transfected with pEGFP-C1 plasmid using LiFect293TM 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 LiFect293TM 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-6xHis plasmid using LiFect293TM In Vitro DNA 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 6xHis 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).