MC-Easy™ Minicircle DNA Production Kit (with Competent Cells)

Easy minicircle production with this kit that provides an efficient way to produce high-quality minicircle DNA (includes competent ZYCY10P3S2T cells).
  • Episomal expression sustained over weeks
  • Foreign DNA-free
  • More efficient transfections from small plasmid size
  • Unlimited insert size
  • Optimized coli minicircle production strain

Products

Catalog Number Description Size Price Quantity Add to Cart
MN920A-1 MC-Easy Minicircle DNA Production Kit (Includes ZYCY10P3S2T producer E. coli strain) 5 Preps $1072
- +
MN925A-1 MC-Easy Minicircle DNA Production Kit (Includes ZYCY10P3S2T producer E. coli strain) 10 Preps $1914
- +

Overview

Overview

Simplify minicircle production with this easy and efficient kit

The MC-Easy™ Minicircle DNA Production Kit enables simple, reproducible, and efficient production of high-quality Minicircle DNA. The finely tuned growth and induction media is optimized for minicircle production, and the included ATP-dependent DNase reagent selectively removes genomic DNA without affecting the quality of the minicircle DNA, for clean and effective minicircle production prep after prep.

Choose from this kit, which comes with the ZYCY10P3S2T E.coli Minicircle Production Competent Cells (Cat.# MN920A-1/MN925A-1), or the kit that does not include competent cells (Cat.# MN910A-1/MN915A-1). For-profit organizations, please see the Product Note at the end of this section.

Our MC-Easy Kits also come with a special minicircle DNA transfection reagent, MC-Fection™, that works well with most cell lines.

About Minicircle Technology
  • Episomal expression sustained over weeks
  • Foreign DNA-free
  • More efficient transfections from small plasmid size
  • Unlimited insert size
  • Optimized coli minicircle production strain
  • Works in vitro and in vivo

When you want sustained transgene expression without introducing any foreign DNA—such as for model animal and gene therapy development—Minicircle Technology is a great gene expression option. Produced as small excised, circular DNA fragments from a parental plasmid, the non-viral, episomal Minicircle expression cassette is free of any bacterial plasmid DNA sequences, and comes with a variety of promoter and reporter combinations. Their small size facilitates more efficient transfection than what’s possible with standard-sized plasmids, and, while Minicircles do not replicate with the host cell, expression lasts for 14 days or longer in dividing cells, and can continue for months in non-dividing cells.

Product Note:

Parental minicircle plasmids and the ZYCY10P3S2T Producer Bacterial Strain are available for purchase by not-for-profit researchers only. Commercial users may purchase pre-made, ready-to-transfect minicircle DNA only. SBI also offers custom parental plasmid cloning and minicircle DNA production to both not-for-profit and commercial end users—contact services@systembio.com for additional details. For any other purposes, including the ability to buy the parental MC production system, commercial users should contact SBI at tech@systembio.com for further information.

MC-Easy Minicircle DNA Production Kit Components

MC-Easy Minicircle DNA Production Kit Components

Minicircle DNA re-purification reagent kit (Endotoxin free water, Minicircle-safe DNase, ATP (25mM), 10X DNase buffer, Precipitation Buffer)
5x Minicircle Growth Medium
5x Induction Medium
MC-Fection transfection reagent for minicircle DNA
Minicircle DNA spin columns
Competent cells, minicircle E. coli producer strain ZYCY10P3S2T (Cat. # MN920A-1 and MN925A-1 only, see Product Note for purchasing restrictions)

How It Works

How It Works

The quick and easy MC-Easy minicircle preparation protocol

Going from parental minicircle plasmid ready-for-maxi-prep pellet is a simple, 2-day process with the MC-Easy Kit:

Day 1
  1. Inoculate 2 mL of LB/Kan with ZYCY10P3S2T Minicircle Production Cells that have already been transformed with the parental minicircle plasmid, and grow for 1 hour at 30°C.
  2. Use the 2 mL culture to inoculate 200 mL of LB/Kan and shake for 16 hours (or overnight) at 30°C.
Day 2
  1. Add 200 mL Induction Medium (included in the MC-Easy Kit), and shake for 5.5 hours at 30°C.
  2. Transfer culture to centrifuge bottle and spin at 1,500g for 15 minutes. Decant media and either continue-on with the minicircle maxiprep, or freeze pellet.
Generating minicircles from the parental cloning vector

To generate minicircles that are ready for transfection, you need your Minicircle Cloning Vector with your insert (gene, promoter-gene cassette, small RNA, etc.), SBI’s optimized, ready-to-transform ZYCY10P3S2T E. coli Minicircle Producer Strain (Cat.# MN900A-1), and arabinose (Cat.# MN850A-1).

Minicircles are produced from the full-sized Parental Minicircle using PhiC31 Integrase, which mediates a recombination event between the PhiC321 attB and attP sites on the parental plasmid (Figure 1). This reaction results in two products—the minicircle, which is now free from any bacterial DNA sequences—and the parental plasmid. To get rid of the parental plasmid, the I-SceI endonuclease recognizes and acts on the I-SceI sites on the parental plasmid, resulting in degradation of the parental plasmid.

How to generate minicircles from the parental minicircle vector

Figure 1. Generating minicircle DNA from the Parental Minicircle Plasmid.

More about the ZYCY10P3S2T E. coli Minicircle Producer Strain

The Minicircle Producer Strain harbors an arabinose-inducible system to express the PhiC31 integrase and the I-SceI endonuclease simultaneously. The ZYCY10P3S2T strain also contains a robust arabinose transporter LacY A177C gene. Adding arabinose to the media turns on expression of the PhiC31 integrase and endonuclease genes, resulting in separation of the Parental Minicircle Plasmid into the individual minicircle and parental plasmids (from the PhiC31 Integrase activity), and the degradation of the parental plasmid (from I-SceI endonuclease activity).

Supporting Data

Supporting Data

Easy and clean minicircle production Clean and easy minicircle production with the MC-Easy Minicircle DNA Production Kit

Figure 1. Easy and clean minicircle production with the MC-Easy Minicircle DNA Production Kit. Note the genomic and parental DNA bands that only appear in the minicircle preps that did not use the MC-Easy Kit.

Achieve sustained expression from minicircles after transfection in vitro and in vivoUse minicircles to get easy, sustained transfection in most cell types

Figure 2. Easy, sustained transfection in most cell types. Transfection of 1 μg of minicircle DNA (pMC.CMV-MCS-EF1-GFPSV40PolyA, Cat.# MN511A-1) into HEK293 cells delivers over one week of robust gene expression.

Use minicircles to express transgenes for weeks in animal models

Figure 3. Express transgenes for weeks in animal models. (A) Hydrodynamic tail vein injection of 2 µg and 4 µg of minicircle DNA (CMV-GFP-Luc) into mice shows excellent expression after 48 hours. (B) Minicircle-delivered transgenes retain robust expression that can last for weeks compared to transgenes that are delivered using plasmid DNA, where expression is rapidly lost. In this study, 40 µg of minicircle DNA was introduced into mice via hydrodynamic tail vein injection.

FAQs

Resources

Citations

  • Johnston, CD, et al. (2019) Systematic evasion of the restriction-modification barrier in bacteria. Proc. Natl. Acad. Sci. U.S.A.. 2019;. PM ID: 31097593
  • Han, D, et al. (2019) Activation of Melatonin Receptor 2 But Not Melatonin Receptor 1 Mediates Melatonin-conferred Cardio-protection Against Myocardial Ischemia/Reperfusion Injury. J. Pineal Res.. 2019;:e12571. PM ID: 30903623
  • Petrini, S, et al. (2017) Aged induced pluripotent stem cell (iPSCs) as a new cellular model for studying premature aging. Aging (Albany NY). 2017; 9(5):1453-1469. PM ID: 28562315
  • Kelton, W, et al. (2017) Reprogramming MHC specificity by CRISPR-Cas9-assisted cassette exchange. Sci Rep. 2017; 7:45775. PM ID: 28374766
  • Traub, S, et al. (2017) Pharmaceutical Characterization of Tropomyosin Receptor Kinase B-Agonistic Antibodies on Human Induced Pluripotent Stem (hiPS) Cell-Derived Neurons. J. Pharmacol. Exp. Ther.. 2017; 361(3):355-365. PM ID: 28351853
  • Liu, N, et al. (2017) PIM1-minicircle as a therapeutic treatment for myocardial infarction. PLoS ONE. 2017; 12(3):e0173963. PM ID: 28323876
  • Zhang, Z, et al. (2017) Gene delivery of TIPE2 inhibits breast cancer development and metastasis via CD8(+) T and NK cell-mediated antitumor responses.. Mol. Immunol.. 2017; 85:230-237. PM ID: 28314212
  • Henno, L, et al. (2017) Analysis of Human Papillomavirus Genome Replication Using Two- and Three-Dimensional Agarose Gel Electrophoresis. Curr Protoc Microbiol. 2017; 45:14B.10.1-14B.10.37. PM ID: 28510360
  • Jaafar, L, et al. (2017) SFPQ•NONO and XLF function separately and together to promote DNA double-strand break repair via canonical nonhomologous end joining. Nucleic Acids Res.. 2017; 45(4):1848-1859. PM ID: 27924002
  • Wu, H, et al. (2017) MicroRNA-206 prevents hepatosteatosis and hyperglycemia by facilitating insulin signaling and impairing lipogenesis. J. Hepatol.. 2017; 66(4):816-824. PM ID: 28025059
  • Tidd, N, et al. (2017) Minicircle Mediated Gene Delivery to Canine and Equine Mesenchymal Stem Cells. Int J Mol Sci. 2017; 18(4). PM ID: 28417917
  • Brett, E, et al. (2017) Magnetic Nanoparticle-Based Upregulation of B-Cell Lymphoma 2 Enhances Bone Regeneration. Stem Cells Transl Med. 2017; 6(1):151-160. PM ID: 28170185
  • Tockner, B, et al. (2016) Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutations. Gene Ther.. 2016; 23(11):775-784. PM ID: 27434145
  • Sun, JG, et al. (2016) Yap1 promotes the survival and self-renewal of breast tumor initiating cells via inhibiting Smad3 signaling. Oncotarget. 2016; 7(9):9692-706. PM ID: 26695440
  • Sharma, VS. (2016) Size controlled retinal differentiation of human induced pluripotent stem cells in shaking microwells. Thesis. 2016;. Link: Thesis
  • Dincer, E, et al. (2016) Canine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey. Vector Borne Zoonotic Dis.. 2016; 16(9):611-8. PM ID: 27400226
  • Gaspar, VM, et al. (2016) Highly selective capture of minicircle DNA biopharmaceuticals by a novel zinc-histidine peptide conjugate. Separation and Purification Technology. 2016; 174:417–424. Link: Separation and Purification Technology
  • Mofid, A. (2016) Ultrasound-Mediated S100A6 Gene Therapy Ameliorates Myocardial Ischemia/Reperfusion (I/R) Injury. Thesis. 2016;. Link: Thesis
  • Fernandes, AR & Chari, DM. (2016) Part II: Functional delivery of a neurotherapeutic gene to neural stem cells using minicircle DNA and nanoparticles: Translational advantages for regenerative neurology. J Control Release. 2016; 238:300-10. PM ID: 27369863
  • Fernandes, AR & Chari, DM. (2016) Part I: Minicircle vector technology limits DNA size restrictions on ex vivo gene delivery using nanoparticle vectors: Overcoming a translational barrier in neural stem cell therapy. J Control Release. 2016; 238:289-99. PM ID: 27317366
MC-Easy™ Minicircle DNA Production Kit (with Competent Cells) $1,072.00

Products

Catalog Number Description Size Price Quantity Add to Cart
MN920A-1 MC-Easy Minicircle DNA Production Kit (Includes ZYCY10P3S2T producer E. coli strain) 5 Preps $1072
- +
MN925A-1 MC-Easy Minicircle DNA Production Kit (Includes ZYCY10P3S2T producer E. coli strain) 10 Preps $1914
- +

Overview

Overview

Simplify minicircle production with this easy and efficient kit

The MC-Easy™ Minicircle DNA Production Kit enables simple, reproducible, and efficient production of high-quality Minicircle DNA. The finely tuned growth and induction media is optimized for minicircle production, and the included ATP-dependent DNase reagent selectively removes genomic DNA without affecting the quality of the minicircle DNA, for clean and effective minicircle production prep after prep.

Choose from this kit, which comes with the ZYCY10P3S2T E.coli Minicircle Production Competent Cells (Cat.# MN920A-1/MN925A-1), or the kit that does not include competent cells (Cat.# MN910A-1/MN915A-1). For-profit organizations, please see the Product Note at the end of this section.

Our MC-Easy Kits also come with a special minicircle DNA transfection reagent, MC-Fection™, that works well with most cell lines.

About Minicircle Technology
  • Episomal expression sustained over weeks
  • Foreign DNA-free
  • More efficient transfections from small plasmid size
  • Unlimited insert size
  • Optimized coli minicircle production strain
  • Works in vitro and in vivo

When you want sustained transgene expression without introducing any foreign DNA—such as for model animal and gene therapy development—Minicircle Technology is a great gene expression option. Produced as small excised, circular DNA fragments from a parental plasmid, the non-viral, episomal Minicircle expression cassette is free of any bacterial plasmid DNA sequences, and comes with a variety of promoter and reporter combinations. Their small size facilitates more efficient transfection than what’s possible with standard-sized plasmids, and, while Minicircles do not replicate with the host cell, expression lasts for 14 days or longer in dividing cells, and can continue for months in non-dividing cells.

Product Note:

Parental minicircle plasmids and the ZYCY10P3S2T Producer Bacterial Strain are available for purchase by not-for-profit researchers only. Commercial users may purchase pre-made, ready-to-transfect minicircle DNA only. SBI also offers custom parental plasmid cloning and minicircle DNA production to both not-for-profit and commercial end users—contact services@systembio.com for additional details. For any other purposes, including the ability to buy the parental MC production system, commercial users should contact SBI at tech@systembio.com for further information.

MC-Easy Minicircle DNA Production Kit Components

MC-Easy Minicircle DNA Production Kit Components

Minicircle DNA re-purification reagent kit (Endotoxin free water, Minicircle-safe DNase, ATP (25mM), 10X DNase buffer, Precipitation Buffer)
5x Minicircle Growth Medium
5x Induction Medium
MC-Fection transfection reagent for minicircle DNA
Minicircle DNA spin columns
Competent cells, minicircle E. coli producer strain ZYCY10P3S2T (Cat. # MN920A-1 and MN925A-1 only, see Product Note for purchasing restrictions)

How It Works

How It Works

The quick and easy MC-Easy minicircle preparation protocol

Going from parental minicircle plasmid ready-for-maxi-prep pellet is a simple, 2-day process with the MC-Easy Kit:

Day 1
  1. Inoculate 2 mL of LB/Kan with ZYCY10P3S2T Minicircle Production Cells that have already been transformed with the parental minicircle plasmid, and grow for 1 hour at 30°C.
  2. Use the 2 mL culture to inoculate 200 mL of LB/Kan and shake for 16 hours (or overnight) at 30°C.
Day 2
  1. Add 200 mL Induction Medium (included in the MC-Easy Kit), and shake for 5.5 hours at 30°C.
  2. Transfer culture to centrifuge bottle and spin at 1,500g for 15 minutes. Decant media and either continue-on with the minicircle maxiprep, or freeze pellet.
Generating minicircles from the parental cloning vector

To generate minicircles that are ready for transfection, you need your Minicircle Cloning Vector with your insert (gene, promoter-gene cassette, small RNA, etc.), SBI’s optimized, ready-to-transform ZYCY10P3S2T E. coli Minicircle Producer Strain (Cat.# MN900A-1), and arabinose (Cat.# MN850A-1).

Minicircles are produced from the full-sized Parental Minicircle using PhiC31 Integrase, which mediates a recombination event between the PhiC321 attB and attP sites on the parental plasmid (Figure 1). This reaction results in two products—the minicircle, which is now free from any bacterial DNA sequences—and the parental plasmid. To get rid of the parental plasmid, the I-SceI endonuclease recognizes and acts on the I-SceI sites on the parental plasmid, resulting in degradation of the parental plasmid.

How to generate minicircles from the parental minicircle vector

Figure 1. Generating minicircle DNA from the Parental Minicircle Plasmid.

More about the ZYCY10P3S2T E. coli Minicircle Producer Strain

The Minicircle Producer Strain harbors an arabinose-inducible system to express the PhiC31 integrase and the I-SceI endonuclease simultaneously. The ZYCY10P3S2T strain also contains a robust arabinose transporter LacY A177C gene. Adding arabinose to the media turns on expression of the PhiC31 integrase and endonuclease genes, resulting in separation of the Parental Minicircle Plasmid into the individual minicircle and parental plasmids (from the PhiC31 Integrase activity), and the degradation of the parental plasmid (from I-SceI endonuclease activity).

Supporting Data

Supporting Data

Easy and clean minicircle production Clean and easy minicircle production with the MC-Easy Minicircle DNA Production Kit

Figure 1. Easy and clean minicircle production with the MC-Easy Minicircle DNA Production Kit. Note the genomic and parental DNA bands that only appear in the minicircle preps that did not use the MC-Easy Kit.

Achieve sustained expression from minicircles after transfection in vitro and in vivoUse minicircles to get easy, sustained transfection in most cell types

Figure 2. Easy, sustained transfection in most cell types. Transfection of 1 μg of minicircle DNA (pMC.CMV-MCS-EF1-GFPSV40PolyA, Cat.# MN511A-1) into HEK293 cells delivers over one week of robust gene expression.

Use minicircles to express transgenes for weeks in animal models

Figure 3. Express transgenes for weeks in animal models. (A) Hydrodynamic tail vein injection of 2 µg and 4 µg of minicircle DNA (CMV-GFP-Luc) into mice shows excellent expression after 48 hours. (B) Minicircle-delivered transgenes retain robust expression that can last for weeks compared to transgenes that are delivered using plasmid DNA, where expression is rapidly lost. In this study, 40 µg of minicircle DNA was introduced into mice via hydrodynamic tail vein injection.

FAQs

Citations

  • Johnston, CD, et al. (2019) Systematic evasion of the restriction-modification barrier in bacteria. Proc. Natl. Acad. Sci. U.S.A.. 2019;. PM ID: 31097593
  • Han, D, et al. (2019) Activation of Melatonin Receptor 2 But Not Melatonin Receptor 1 Mediates Melatonin-conferred Cardio-protection Against Myocardial Ischemia/Reperfusion Injury. J. Pineal Res.. 2019;:e12571. PM ID: 30903623
  • Petrini, S, et al. (2017) Aged induced pluripotent stem cell (iPSCs) as a new cellular model for studying premature aging. Aging (Albany NY). 2017; 9(5):1453-1469. PM ID: 28562315
  • Kelton, W, et al. (2017) Reprogramming MHC specificity by CRISPR-Cas9-assisted cassette exchange. Sci Rep. 2017; 7:45775. PM ID: 28374766
  • Traub, S, et al. (2017) Pharmaceutical Characterization of Tropomyosin Receptor Kinase B-Agonistic Antibodies on Human Induced Pluripotent Stem (hiPS) Cell-Derived Neurons. J. Pharmacol. Exp. Ther.. 2017; 361(3):355-365. PM ID: 28351853
  • Liu, N, et al. (2017) PIM1-minicircle as a therapeutic treatment for myocardial infarction. PLoS ONE. 2017; 12(3):e0173963. PM ID: 28323876
  • Zhang, Z, et al. (2017) Gene delivery of TIPE2 inhibits breast cancer development and metastasis via CD8(+) T and NK cell-mediated antitumor responses.. Mol. Immunol.. 2017; 85:230-237. PM ID: 28314212
  • Henno, L, et al. (2017) Analysis of Human Papillomavirus Genome Replication Using Two- and Three-Dimensional Agarose Gel Electrophoresis. Curr Protoc Microbiol. 2017; 45:14B.10.1-14B.10.37. PM ID: 28510360
  • Jaafar, L, et al. (2017) SFPQ•NONO and XLF function separately and together to promote DNA double-strand break repair via canonical nonhomologous end joining. Nucleic Acids Res.. 2017; 45(4):1848-1859. PM ID: 27924002
  • Wu, H, et al. (2017) MicroRNA-206 prevents hepatosteatosis and hyperglycemia by facilitating insulin signaling and impairing lipogenesis. J. Hepatol.. 2017; 66(4):816-824. PM ID: 28025059
  • Tidd, N, et al. (2017) Minicircle Mediated Gene Delivery to Canine and Equine Mesenchymal Stem Cells. Int J Mol Sci. 2017; 18(4). PM ID: 28417917
  • Brett, E, et al. (2017) Magnetic Nanoparticle-Based Upregulation of B-Cell Lymphoma 2 Enhances Bone Regeneration. Stem Cells Transl Med. 2017; 6(1):151-160. PM ID: 28170185
  • Tockner, B, et al. (2016) Construction and validation of an RNA trans-splicing molecule suitable to repair a large number of COL7A1 mutations. Gene Ther.. 2016; 23(11):775-784. PM ID: 27434145
  • Sun, JG, et al. (2016) Yap1 promotes the survival and self-renewal of breast tumor initiating cells via inhibiting Smad3 signaling. Oncotarget. 2016; 7(9):9692-706. PM ID: 26695440
  • Sharma, VS. (2016) Size controlled retinal differentiation of human induced pluripotent stem cells in shaking microwells. Thesis. 2016;. Link: Thesis
  • Dincer, E, et al. (2016) Canine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey. Vector Borne Zoonotic Dis.. 2016; 16(9):611-8. PM ID: 27400226
  • Gaspar, VM, et al. (2016) Highly selective capture of minicircle DNA biopharmaceuticals by a novel zinc-histidine peptide conjugate. Separation and Purification Technology. 2016; 174:417–424. Link: Separation and Purification Technology
  • Mofid, A. (2016) Ultrasound-Mediated S100A6 Gene Therapy Ameliorates Myocardial Ischemia/Reperfusion (I/R) Injury. Thesis. 2016;. Link: Thesis
  • Fernandes, AR & Chari, DM. (2016) Part II: Functional delivery of a neurotherapeutic gene to neural stem cells using minicircle DNA and nanoparticles: Translational advantages for regenerative neurology. J Control Release. 2016; 238:300-10. PM ID: 27369863
  • Fernandes, AR & Chari, DM. (2016) Part I: Minicircle vector technology limits DNA size restrictions on ex vivo gene delivery using nanoparticle vectors: Overcoming a translational barrier in neural stem cell therapy. J Control Release. 2016; 238:289-99. PM ID: 27317366