SCIENTZ

Gene Electroporator

Code SCIENTZ-2CS
Bench-top gene electroporation system that uses a transient, microprocessor-controlled high-voltage pulse (exponential decay, 401–3000 V) to permeabilise the cell membrane and introduce DNA, RNA, siRNA, proteins and other molecules into bacteria, yeast, mammalian and plant cells.
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Features

SCIENTZ-2CS Gene Electroporator

The SCIENTZ-2CS Gene Electroporator consists of the main unit, a gene electroporation cup and dedicated connecting cables. It uses electroporation to introduce DNA into competent cells, plant and animal cells, and yeast cells. Compared with other transformation methods, it offers high repeatability, high efficiency, ease of operation and precise control, and because electroporation is a physical rather than a chemical or viral process, it causes negligible genotoxicity.

Working Principle

Electroporation (cellular electroporation) introduces exogenous macromolecules – DNA, RNA, siRNA and proteins, as well as small molecules – into cells. Under a transient, strong electric field, the cell membrane becomes temporarily permeable, allowing charged exogenous substances to cross it in a manner similar to electrophoresis. Because the phospholipid bilayer has high resistance, most of the applied voltage is borne by the membrane itself, with minimal voltage reaching the cytoplasm; the voltage at the nuclear membrane is close to zero, which keeps genotoxicity negligible. Since the process is physical rather than chemical, the molecular properties of the cell surface have little effect on it, so the SCIENTZ-2CS can be applied to virtually any cell type and its results are easily quantifiable.

Features

  • High efficiency – short transformation time, high conversion rate, small tolerance
  • Intelligent storage – experimental parameters can be stored for future use
  • Precise control – microprocessor-controlled pulse discharge
  • Aesthetic, integrated design – intuitive touchscreen display, simple operation

Technical Parameters

  • Pulse type: exponential decay
  • High voltage output: 401–3000 V
  • Low voltage output: 50–400 V
  • High voltage capacitance: 10 / 25 / 35 / 50 / 60 µF
  • Low voltage capacitance: 50–1560 µF, in 25 µF steps
  • Parallel resistance: 50–1650 Ω, in 50 Ω steps
  • Control system: microcomputer-controlled, with adjustable RC time constant
  • Main unit dimensions: 40 × 30 × 20 cm; net weight 5.5 kg

Standard System Configuration

Main unit, gene electroporation cup, dedicated connecting cables.

Indicative Electroporation Parameters by Organism

OrganismPulse voltage (V)Resistance (Ω)Capacitance (µF)Cup (mm)
E. coli1800200251
E. coli2500200252
E. coli3000200252
A. tumefaciens2400200251
P. aeruginosa2500200252
S. aureus2900100252
B. cereus1000200252
S. pyogenes2100200502
L. plantarum2000400252
S. cerevisiae1500200252
S. pombe2300200252
C. albicans1500200252
P. pastoris2000200252

Note: parameters vary between labs and are provided for reference only.

Applications of SCIENTZ-2CS Gene Electroporator

  • Electroporation of bacteria, yeast and other microorganisms
  • Transfection of mammalian cells, plant tissues and protoplasts
  • Cell hybridisation and gene fusion
  • Introduction of marker genes for labelling and indicating purposes
  • Introduction of drugs, proteins, antibodies and other molecules for studying cellular structure and function

Typical fields of use include the food industry, agricultural sciences, veterinary research and bioengineering.

Specifications
  • Pulse type: exponential decay
  • High voltage output: 401-3000V
  • Low voltage output: 50-400V
  • High voltage capacitance: 10/25/35/50/60 µF
  • Low voltage capacitance: 50-1560 µF in 25 µF steps
  • Parallel resistance: 50-1650Ω in 50Ω steps
  • Control system: microcomputer control, adjustable RC time constant
  • Main unit dimensions: 40x30x20cm
  • Net weight: 5.5kg
  • Packaging dimensions: 58x36x25cm
Publications
1. LI J, ZHANG S, GAO L, et al. A cell-based high-throughput assay for the screening of small-molecule inhibitors of p53-MDM2 interaction. Journal of Biomolecular Screening, 2011. 2. ZHANG S Y, LI J, XIE X. Discovery and characterization of novel small molecule agonists of G protein-coupled receptor 119. Acta Pharmacologica Sinica, 2014.