TransIT¢ç-LT1 Transfection Reagent
CAT# PRODUCT SIZE STORAGE ¼ÒºñÀÚ°¡ ÁÖ¹®
MIR2304TransIT¢ç-LT1 Transfection Reagent0.4 ml-·Î±×ÀÎ
MIR2300TransIT¢ç-LT1 Transfection Reagent1 ml-·Î±×ÀÎ
MIR2305TransIT¢ç-LT1 Transfection Reagent5 X 1 ml-·Î±×ÀÎ
MIR2306TransIT¢ç-LT1 Transfection Reagent10 X 1 ml-·Î±×ÀÎ
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TransIT¢ç-LT1 Transfection Reagent

A broad spectrum, low toxicity, DNA transfection reagent

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  • °íÈ¿À² ¿î¹Ý - ´Ù¾çÇÑ ¼¼Æ÷¿¡ È¿°úÀûÀÎ DNA Àü´Þ.
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  • °æÁ¦ÀûÀÎ °¡°Ý - ÇϳªÀÇ transfection ½Ã¾àÀ¸·Î ´Ù¾çÇÑ ¼¼Æ÷¿¡ Àû¿ë °¡´É.
 
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Figure 1. High Efficiency Transfection of iCell¢ç Cardiomyocytes using TransIT¢ç-LT1 Transfection Reagent. iCell Cardiomyocytes were plated at 20,000 cells/well in a 96 well tissue culture plate coated with 0.1% gelatin. After allowing the cells to recover from thaw, cells were transfected with 100 ng/well of pMAXGFP (Lonza) using TransIT¢ç-LT1 Transfection Reagent with a 2:1 reagent-to-DNA ratio according to the manufacturer¡¯s instructions. Fluorescent images were taken 3 days post transfection using a Olympus IX71¢ç inverted microscope. See more information on stem cell applications.
 
Figure 2. The TransIT¢ç-LT1 Reagent Exhibits Higher Expression and Lower Cellular Toxicity Compared to Other Transfection Reagents. HepG2 cells were transfected with a luciferase expression plasmid using the designated reagents at the manufacturer¡¯s recommended reagent-to-DNA ratio indicated beneath each bar. Transfections were performed in 96-well plates using 0.1 µg of plasmid DNA per well. Luciferase expression (bar graph) and lactate dehydrogenase (LDH) levels (line graph) were measured at 24 hours post-transfection. LDH levels are reported as % cytotoxicity compared to cells alone and were measured using a commercially available colorimetric assay; all values at or below zero are represented as zero on graph. Experiments were performed as per industry accepted testing protocols. FuGENE is a registered trademark of Fugent LLC. Lipofectamine is a trademark of Life Technologies Corporation.
 
 
Figure 3. Comparable Luciferase Expression with the TransIT¢ç-LT1 Reagent and FuGENE¢ç 6 in Multiple Cell Types. The indicated cell lines were transfected in duplicate with 1 µg of a luciferase expression vector per well of a 12-well plate using either 3 µl of the TransIT¢ç-LT1 or FuGENE¢ç 6 Reagents according to industry accepted testing protocols. Cells were harvested 24 hours post-transfection and assayed for luciferase activity. FuGENE is a registered trademark of Fugent LLC.

Figure 4. The TransIT¢ç-LT1 Reagent Efficiently Delivers DNA to a Wide Variety of Cell Lines. Using the TransIT¢ç-LT1 Transfection Reagent, cells were transfected with the pEGFP-C1 expression vector, and the percentage of EGFP expressing cells was determined 24-48 hours post-transfection.

Storage Conditions: Store at 4¡ÆC
Product Guarantee: 1 year

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