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TransPass™ D2 Transfection Reagent |
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Prices are in US dollars and valid only for US orders.
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Description:
The TransPass D2 Transfection Reagent is a non-lipid cationic polymer designed for transfecting plasmid DNA into many mammalian cell lines including primary cell lines and endothelial cell lines. Complex co-transfections of many plasmids can be efficiently transfected using the TransPass D2 Transfection Reagent.
Cell Lines Successfully Transfected:
A549, CHO-K1, COS, HCT116, HEK293, HeLa, HepG2, HL60, Jurkat, MCF-7, MDA, NIH3T3 and U20S.
Figure 1: Human Umbilical Vein Endothelial Cells (HUVEC) transfected with a plasmid expressing GFP using TransPass D2 Transfection Reagent.
Figure 2: Titration of TransPass D2 Transfection Reagent in CHO-K1 cells using Protocol 1 and secreted Gaussia luciferase (pCMV-GLuc) as a reporter. Transfections contain 0.7 µg pCMV-GLuc and 250 µl plating medium (10%FBS-F12K) per well. The values obtained from the transfections with the indicated amounts of TransPass D2 Transfection Reagent were obtained from 20 µL of culture medium 24 hr post transfection.
Background:
The introduction of recombinant DNA into cultured cells or "transfection", has become an essential tool for studying gene function and regulation. Initially, cells were transfected by methods such as Calcium Phosphate co-precipitation, electroporation or viral factors (1, 2). The introduction of cationic lipids or polymers as transfection agents has led to the development of reagents that efficiently deliver DNA through the cell membrane and into the nucleus (3).
Transfection Guidelines:
For consistent results, it is important to maintain healthy proliferating cells that are regularly passaged.
It is important that NO heparin and NO antibiotics/antimycotics in the growth medium during transfection.
Use sterile plasmid DNA that is purified by CsCl gradient centrifugation or column chromatography.
The following parameters can be optimized in order in order to maximize the transfection efficiency for a particular cell line: the cell density at the time of transfection, amount of transfection reagent, amount of plasmid DNA and the culture incubation time before analysis must be optimized.
Reaction & Storage Conditions
Storage Temperature:
4°C
Do not freeze.
Notes
Usage notes:- For most cell lines try Protocol 1 first (transfection in the presence of serum). Keep the amount of plasmid DNA constant while varying the amount of TransPass D2 Transfection Reagent. Once the optimal ratio (transfection reagent to DNA) is established, the amount of plasmid DNA and transfection reagent can be increased. Use Table 1 as a guide to optimize the transfection protocol for different plate formats. A convenient method for optimizing transfection conditions is to use pCMV-GLuc Control Plasmid (NEB #N8081), which contains the gene for the secreted Gaussia luciferase.
- For both Protocols 1 and 2, serum-free medium is required to form the transfection complexes (Step 2).
- Multiple plasmids can be combined (step 2) and simultaneously transfected. For consistent results, the total amount of transfected DNA should stay the same between different wells.
- If you are using Protocol 2 and the cells are sensitive to prolonged absence of serum, the exposure to the serum-free medium can be minimized by decreasing the incubation time (Step 7).
- For suspension cells, the following protocol (modification of Protocol 1) is recommended:
Prepare the plasmid/TransPass D2 complex in 0.5 ml serum-free medium per well of a 12-well plate. Incubate at room temperature for 20?30 minutes. Immediately prior to adding transfection complex (step 5 of Protocol 1), spin down cells to be transfected and resuspend them in high glucose DMEM at a density of 5 x 106 cells per ml. Aliquot 100 µl of cell suspension per well of a 12-well plate and add 0.5 ml of the transfection complex. Rock the plate gently in order to evenly disperse the complex mixture and incubate the cells for two hours. Add complete media with serum as follows: 2 ml per well for a 6-well plate, 1 ml per well for a 12-well plate and 0.5 ml per well for a 24-well plate.
Protocols
Protocols for TransPass™ D2 Transfection Reagent
Quality Control for Current Lot
Quality control values for a specific lot can be found on the datacard which accompanies each product.
Quality Assurance Statement:
Each lot of TransPass D2 Transfection Reagent is tested for efficient delivery of two different reporter plasmids expressing luciferase in CHO cells.
References
- Sambrook, J., Fritsch, E. F. and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, (2nd ed.), Cold Spring Harbor: Cold Spring Harbor Laboratory .
- Ausubel, F. M. et al. (1987) Current Protocols in Molecular Biology, (2nd ed.), New York: Greene Publishing Associates and Wiley- .
- Felgner P.L. et al. (1987) Proc. Natl. Acad. Sci. USA, 84, 7413-7417.
Companion Products
BioLux™ Gaussia Luciferase Assay Kit
Luciferase Cell Lysis Buffer
pCMV-GLuc Control Plasmid
pGLuc-Basic Vector
pNEBR-R1 Regulator Plasmid
pNEBR-X1 Vector
pNEBR-X1GLuc Control Plasmid
pNEBR-X1Hygro Vector
RheoSwitch® Mammalian Inducible Expression System
TransPass™ D1 Transfection Reagent
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New
England Biolabs, Inc. is an ISO 9001 and ISO
14001 Certified Company.
NEB certifies that it is a small business in accordance with the US Small Business Administration and 13 CFR 121.201 |
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