QIAGEN Plasmid Plus Kits
For the fastest, most convenient purification of up to 10 mg transfection-grade plasmid DNA
For the fastest, most convenient purification of up to 10 mg transfection-grade plasmid DNA
✓ 24/7 automatic processing of online orders
✓ Knowledgeable and professional Product & Technical Support
✓ Fast and reliable (re)-ordering
Cat. No. / ID: 12941
✓ 24/7 automatic processing of online orders
✓ Knowledgeable and professional Product & Technical Support
✓ Fast and reliable (re)-ordering
The QIAGEN Plasmid Plus Kits enable ultrafast, large-scale purification of up to
10 mg of highly pure plasmid DNA. The use of a vacuum manifold allows purification of up to 24 samples in parallel, reducing hands-on time. Low elution volumes yield highly concentrated plasmid DNA for direct use without ethanol precipitation. The QIAGEN Plasmid Plus Kits also feature a dedicated wash buffer for endotoxin reduction. The plasmid DNA obtained is highly suitable for a multitude of applications, including transfection into sensitive cell lines.
For optimal results it is recommended to use this product together with QIAvac 24 Plus.
Want to try this solution for the first time? Request a quote for a trial kit.
QIAGEN Plasmid Plus technology delivers the same performance and quality as anion-exchange technology. The unique binding chemistry of the QIAGEN Plasmid Plus columns ensures that pure plasmid DNA is obtained every time. High-yield protocols and extra buffer volumes are provided with the QIAGEN Plasmid Plus Kits. Yields of up to 10 mg (giga),
2 mg (mega), 1 mg (maxi), and 250 μg (midi) of highly pure plasmid DNA, free of contaminants such as RNA, proteins, and genomic DNA are achieved (see figures " High yields are ensured with QIAGEN Plasmid Plus Kits (QPP)" and " Analytical chromatogram").
Endotoxins, also known as lipopolysaccharides or LPS, are cell-membrane components of Gram-negative bacteria such as E. coli and are released during the lysis step of plasmid purification. Endotoxins can induce nonspecific activation of immune responses, and thus represent a noncontrollable variable in transfection experiment setup, influencing the outcome and reproducibility of results and making them difficult to compare and interpret.
The endotoxin wash buffer provided in the kits reduces bacterial endotoxins to levels usually below 1 EU/μg DNA. (Endotoxin levels can vary depending on the host strain, culture media, and cell density. If the cell density is very high, endotoxin levels may be slightly higher, ranging from 1–3 EU/μg DNA.) This makes the plasmid DNA suitable for a multitude of applications, including transfection into sensitive cell lines (see figures " Endotoxin levels using QIAGEN Plasmid Plus Kits", " Endotoxin levels using different isolation methods", and " Efficient transfection in sensitive cell lines").
The QIAGEN Plasmid Plus Kits provide the most convenient method for large-scale plasmid preparation. The design and unique binding chemistry of the QIAGEN Plasmid Plus columns allow a simple bind-wash-elute procedure based on a novel chemistry. This procedure makes these kits the fastest large-scale prep available — 20 minutes for maxi and midi preps. The resulting plasmid DNA is highly concentrated and ready for immediate use in subsequent applications without further ethanol precipitation. Thus, the plasmid DNA is highly suitable for applications that only allow small reaction volumes.
LyseBlue, an optional color indicator that provides visual identification of optimum buffer mixing, is also included in the kit. This prevents common handling errors that lead to inefficient cell lysis and incomplete precipitation of SDS, genomic DNA, and cell debris. Through a simple color change, this unique buffer additive ensures that optimum cell lysis and neutralization is achieved, maximizing yields.
Features | Plasmid Plus Giga Kit | Plasmid Plus Mega Kit | Plasmid Plus Maxi Kit | Plasmid Plus Midi Kit |
---|---|---|---|---|
Applications | Transfection of most cell lines, cloning, enzymatic restriction, in-vitro translation/transcription, sequencing | Transfection of most cell lines, cloning, enzymatic restriction, in-vitro translation/transcription, sequencing | Transfection of most cell lines, cloning, enzymatic restriction, in-vitro translation/transcription, sequencing | Transfection of most cell lines, cloning, enzymatic restriction, in-vitro translation/transcription, sequencing |
Culture volume/starting material | 2500 ml culture volume | 500 ml culture volume | 50–200 ml culture volume | 25–50 ml culture volume |
Final DNA concentration | ≥1 µg/µl | ≥1 µg/µl | ≥1 µg/µl | ≥1 µg/µl |
Plasmid type | Plasmids, cosmids | Plasmids, cosmids | Plasmids, cosmids | Plasmids, cosmids |
Processing | Manual (centrifugation and vacuum), parallel processing | Manual (centrifugation and vacuum), parallel processing | Manual (centrifugation and vacuum), parallel processing | Manual (centrifugation and vacuum), parallel processing |
Samples per run; throughput | 1–12 samples per run | 1–12 samples per run | 1–24 samples per run | 1–24 samples per run |
Technology | Advanced silica technology (non-chaotrophic), endotoxin reduction | Advanced silica technology (non-chaotrophic), endotoxin reduction | Advanced silica technology (non-chaotrophic), endotoxin reduction | Advanced silica technology (non-chaotrophic), endotoxin reduction |
Time per run | 50 min | 40 min | 20 min | 20 min |
Yield | up to 10 mg | up to 2.5 mg | up to 1 mg | up to 250 µg |
QIAfilter cartridges provided in QIAGEN Plasmid Plus Kits enable rapid lysate clearing. Loading of the cleared lysate onto the column can be performed in one step, saving time. A vacuum manifold (such as the QIAvac 24 Plus) is used to draw the cleared lysate and subsequent wash buffers through the QIAGEN Plasmid Plus column. Following the washing and drying of the membrane, the highly concentrated DNA is eluted in low volumes by centrifugation (see flowchart " QIAGEN Plasmid Plus procedure").
The QIAGEN Plasmid Plus Kits provide transfection-grade plasmid DNA highly suited for all applications, such as: