TransIT-X2¢â Dynamic Delivery System
CAT# PRODUCT SIZE STORAGE ¼ÒºñÀÚ°¡ ÁÖ¹®
MIR6003[Mirus]TransIT-X2¢â Dynamic Delivery System0.3 ml-·Î±×ÀÎ
MIR6004[Mirus]TransIT-X2¢â Dynamic Delivery System0.75 ml-·Î±×ÀÎ
MIR6000[Mirus]TransIT-X2¢â Dynamic Delivery System1.5 ml-·Î±×ÀÎ
MIR6005[Mirus]TransIT-X2¢â Dynamic Delivery System5 x 1.5 ml-·Î±×ÀÎ
MIR6006[Mirus]TransIT-X2¢â Dynamic Delivery System10 x 1.5 ml-·Î±×ÀÎ
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NEW! TransIT-X2¢â Dynamic Delivery System

A novel, polymeric system for efficient delivery of plasmid DNA and/or siRNA/miRNA

 
TransIT-X2 Dynamic Delivery SystemÀº non-liposomal, polymeric systemÀ» ÀÌ¿ëÇÏ¿© primary cellÀ» Æ÷ÇÔÇÑ ´Ù¾çÇÑ cell type¿¡ ¶Ù¾î³­ È¿À²À» º¸ÀÔ´Ï´Ù.
TransIT-X2 Dynamic Delivery SystemÀº DNA¿Í siRNA/miRNAÀÇ °¢°¢ÀÇ transfection¿¡ ÀÌ¿ëÇÒ ¼ö ÀÖÀ¸¸ç, DNA¿Í siRNA/miRNA transfection °¡´ÉÇÕ´Ï´Ù.
TransIT-X2 Àº transfectionÈÄ¿¡ ¹èÁö ±³È¯ ÇÊ¿äÇÏÁö ¾ÊÀ¸¸ç, serumÀÌ Æ÷ÇÔµÈ ¹èÁö¿¡¼­ transfectionÀÌ °¡´ÉÇÕ´Ï´Ù.
TransIT-X2 Dynamic Delivery SystemÀº °ÅÀÇ ¸ðµç cell type¿¡¼­ transfectionÀÌ Lipofectamine2000 Á¦Ç°º¸´Ù ¿ì¼öÇÑ ¼º´ÉÀ» °¡Áö°í ÀÖ½À´Ï´Ù.
 
  • È¿À² ±¤¹üÀ§ÇÑ ¹üÀ§ÀÇ ¼¼Æ÷ÀÇ transfectionÀÌ ¿ì¼öÇÔ.
  • Àüȯ plasmid DNA¿Í siRNA co-transfection °¡´É.
  • ±â¼ú µ¶Ã¢ÀûÀÎ non-liposomal, polymeric technology.
Figure 1:Visualization of High GFP Expression using TransIT-X2¢â Dynamic Delivery System
Figure 1. Visualization of High GFP Expression using TransIT-X2¢â Dynamic Delivery System. TransIT-X2¢â Dynamic Delivery System was used to transfect plasmid DNA encoding EGFP into A549, CHO-K1, HepG2, LNCaP, MDCK, PC12, primary human mammary epithelial cells (HMEC) and normal human dermal fibroblasts (NHDF). Transfections were performed in 35 mm MatTek dishes using 4-8 µl of TransIT-X2¢â to deliver 2 µg of DNA. Images (32X) were captured at 48 hours post-transfection using a Zeiss Axiovert S100 inverted fluorescence microscope.

* indicates primary cell types
Figure 2. High GFP Transfection Efficiency in Multiple Cell Lines and Primary Cells using TransIT-X2¢â Dynamic Delivery System. TransIT-X2¢â Dynamic Delivery System was used to transfect plasmid DNA encoding EGFP into A549, CHO-K1, Hep G2, MDCK, LNCaP, PC-12, primary human mammary epithelial cells (HMEC) and normal human dermal fibroblasts (NHDF). Transfections were performed in 96-well plates using 0.2-0.4 µl of TransIT-X2¢â to deliver 0.1 µg of DNA (2:1, 3:1 or 4:1 reagent: DNA ratio). Triplicate wells were assayed 48 hours post-transfection using guava easyCyte¢â 5HT Flow Cytometer.

*indicates primary cell types
 
Figure 3. Functional Co-delivery of Plasmid DNA and siRNA using the TransIT-X2¢â¢â Dynamic Delivery System. TransIT-X2¢â Dynamic Delivery System was used to transfect plasmid Cy¢ç5 labeled DNA encoding nuclear YFP and Cy¢ç3 labeled siRNA into HeLa cells. Transfection was performed in 6-well plates with Poly-L-Lysine (PLL) coated coverslips using 4 µl of TransIT-X2¢â to deliver 2 µg of DNA and 25 nM siRNA (2:1 reagent:DNA ratio). Actin cytoskeleton was stained using Alexa Fluor¢ç 350 Phalloidin. Images (63X) were captured at 24 hours post-transfection using a Nikon A1R confocal microscope. Image key: yellow (nuclear YFP), blue (Cy¢ç5 labeled DNA), red (Cy¢ç3 labeled siRNA), green (actin cytoskeleton).
 
Figure 4. TransIT-X2¢â Dynamic Delivery System Achieves Higher Knockdown than Lipofectamine¢ç 2000. TransIT-X2¢â Dynamic Delivery System and Lipofectamine¢ç 2000 Transfection Reagent were used to transfect siRNA targeting endogenous proteins – GAPDH and AHA1 or to deliver a non-targeting siRNA control in normal human dermal fibroblasts (NHDF). Cells were transfected in a 6-well plate using 4 µl of TransIT-X2¢â or 6 µl of Lipofectamine¢ç 2000 and 25 nM siRNA according to each manufacturer's protocol. The amount of GAPDH or AHA1 mRNA was measured relative to 18s rRNA levels using qRT-PCR and then normalized to the mRNA levels of the non-targeting control, 48 hours post-transfection. Error bars represent the standard deviation of triplicate wells.
 
 
Figure 5. Effective miRNA Delivery using TransIT-X2¢â Dynamic Delivery System Yields Decreased Levels of PTK9 mRNA. TransIT-X2¢â Dynamic Delivery System and Lipofectamine¢ç¢ç 2000 Transfection Reagent were used to transfect Pre-miR¢â hsa-miR-1 miRNA Precursor or mirVana¢â miRNA mimic, miR-1, both known to decrease PTK9 mRNA levels. A Pre-miR negative control was also transfected to assess baseline mRNA levels. T47D cells were transfected in a 12-well plate using 3 µl of TransIT-X2¢â or Lipofectamine¢ç 2000 and 50 nM miRNA according to each manufacturer's protocol. The amount of PTK9 mRNA was measured relative to 18s rRNA levels using qRT-PCR and then normalized to the mRNA levels of the negative control, 48 hours post-transfection.  Error bars represent the standard deviation of triplicate wells.
Storage Conditions: Store at -20¡ÆC
Product Guarantee: 6 months
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X2 »ç¿ë Èıâ - ¿øÀÚ·ÂÀÇÇпø ¼­OO¹Ú»ç´Ô (A549 cell)
cell viability ºñ±³ ½ÇÇè - lipofectamine 2000°ú X2
siRNA delivery test - RNAimax¿Í x2 ºñ±³ ½ÇÇè. (A549)
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TransIT¢ç-2020 Transfection Reagent
TransIT¢ç-LT1 Transfection Reagent
TransIT-TKO¢ç Transfection Reagent
TransIT-siQUEST¢ç Transfection Reagent
MiraCLEAN¢ç Endotoxin Removal Kit
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