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NEPA21 Electroporator
ELEPO21 Electroporator
NEPA Porator
ECFG Porator
Transgenic Mouse Zygote Electroporation: NEPA21
Organoid Electroporation: NEPA21
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Hybridoma Production for Monoclonal Antibodies
Bacteria / Yeast Electroporation
SP100: Sonoporator
NEPA21: Illustrated  Applications
NEPA21: Publications by   Research Application
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- CU700: Monitoring System
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- KTAC-4000: Sonoporator
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Electroporation and Electro   Cell Fusion Accessories
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Featured Applications
SONIDEL SP100 and KTAC4000
Electro Cell Fusion
LF101 and LF201

Featured Device

Product Code: SONIDEL STK10

Desc:Ultrasound Transfection Positive Control
Applic:Sonoporation Transfection Kit

Featured Electrode

Product Code: CUY650P1-5X8

Electrodes for Electroporation
Tweezers with 1mmφ platinum disk & 5mm◊8mm platinum ellipse electrodes

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Rat knockout

Organoid EP ‚Äď with the NEPA21 System
We have had considerable success with the NEPA21 system for Organoid EP.

Methodology and Publications
–¬†¬† ¬†Modelling colorectal cancer using CRISPR-Cas9-mediated engineering of human intestinal organoids
o¬†¬† Toshiro Sato, et al ‚Äď June 2014
o    In this paper, the authors dissociated human colonic organoids into single cells and electroporated using the NEPA21 and cuvettes
o    RESULTS: Liver Organoid Results РCuvette EP (with the NEPA21 and our EC-002S Cuvettes)

–¬†¬† ¬†Efficient genetic engineering of human intestinal organoids using electroporation
o¬†¬† ¬†Toshiro Sato, et al ‚Äď September 2015
o    This paper is an optimisation of the previously developed  organoid  culture  protocol  presented in the earlier paper
o    In this paper, the authors describe a method for modulating genes of interest in untransformed human colonic organoids via electroporation of gene vectors.
o    This paper presents a detailed (step-by-step) protocol for the generation of intestinal organoids by culture with essential growth factors in a basement membrane matrix.
o    The paper also describes how to stably integrate genes via the piggyback transposon, as well as precise genome editing using the crispr-cas9 system.
o    Beginning with crypt isolation from a human colon sample, genetically modified organoids can be obtained in 3 week.  Isolated intestinal crypts to be expanded for over a year with the addition of essential growth factors and after embedding into basement membrane matrix (Matrigel)
o    Under the described culture  conditions, the intestinal stem cells organize into 3D crypt-villus structures named intestinal epithelial organoids. This provides a source of untransformed human intestinal cells that are independent of pre-existing cell lines
o    Comparative evaluation of various gene delivery methods, showed that the electroporation method, combined with several modifications to  the  culture  conditions,  yielded  relatively  high  transduction efficiency   compared   with   liposomal   transfection   or   gene electrotransfer using nucleofector
o    An additional advantage of the presented electroporation method is that genes can be transferred upon preparation of the plasmids, which alleviates the labour and time that are required to produce lentivirus or transgenic rodents

Recommended Electrodes
The above papers use:
–¬†¬† ¬†the NEPA21 electroporator
–¬†¬† ¬†our EC-002S cuvettes
–¬†¬† ¬†CU500 Cuvette Chamber and
–¬†¬† ¬†CU600 Cuvette Stand


Further Organoid Information
Clients report successful electroporation of organoids in matrigel drops.
We have sold clients the following electrode configurations to support their wider organoid research:
–¬†¬† ¬†CUY900-13-3-5
–¬†¬† ¬†CUY520P5
–¬†¬† ¬†CUY701P10E and CUY701P7L
o    The methodology used for this electrode combination is similar to the method recommended for Brain Slice EP


Other Relevant links to our website
–¬†¬† ¬†Oviduct EP ‚Äď GONAD Technique
–¬†¬† ¬†Rat Knockout ‚Äď Zygote and Oocyte EP
–¬†¬† ¬†Intestine/Gut EP ‚Äď (In vivo and Ex Vivo)
–¬†¬† ¬†Liver EP
–¬†¬† ¬†ES_iPSCells – Transfection Data


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