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Featured Device

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Product Code: SONIDEL SP100

Desc:Sonoporator
Applic:(hover for application)Application:
  • Delivery of plasmids to cells and tissues for gene therapy-based applications and studies.
  • Delivery of nucleic acids such as siRNA, RNAi etc. to cells and tissues for studies on control of gene expression/gene therapy.
  • Delivery of cancer chemotherapeutic agents to impermeable target cells/tissues.
  • Delivery of agents to cells to study metabolic effects.


Featured Electrode



Product Code: CUY5100-25

Application:
Electrodes for Electro Cell Fusion
Description:
Chopstick Stainless Steel, needle electrode, 25µmφ, 5mm tip length, 2/pkg

Information
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Search Results
Your search for "650" returned 766 results. (Duplicates have been removed)

Sonidel Product Search Results (21 results)

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CUY650-5
Tweezers with 5mmφ disk electrodes
 
CUY650-7
Tweezers with 7mmf disk electrodes
 
CUY650-10
Tweezers with 10mmf disk electrodes
 
CUY650P0.5
Tweezers with 0.5mmφ platinum disk electrodes
 
CUY650P1
Tweezers with 1mmφ platinum disk electrodes
 
 

Sonidel Article Search Results (736 results)

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Mouse/Rat – Muscle
Since no surgery is involved, the researcher can easily perform electroporation and do so consecutively in a short period of time.  In our opinion, this is the best method.  However, as the volume of muscle affects the resistance value, and thus, actual…
 
In Utero Electroporation
As evident from the review by H Tabata and K Nakajima in their book ‘Electroporation and Sonoporation in Developmental Biology’, (Chapter 14, In Utero Electroporation: Assay System for Migration of Cerebral Cortical Neurons, p 143 – 152), the optimal…
 
In Utero Electroporation
As evident from the review by H Tabata and K Nakajima in their book ‘Electroporation and Sonoporation in Developmental Biology’, (Chapter 14, In Utero Electroporation: Assay System for Migration of Cerebral Cortical Neurons, p 143 – 152), the optimal…
 
Zebrafish Retina Electrode Recommendation
For Larval Zebrafish Retina (which is quite small, 10microns) it may not be possible to inject DNA buffer.   Accordingly, we suggest that electroporation is performed after the larval zebrafish eye is taken out.  Once this is done and one intends…
 
Zebrafish Fin Electrode Recommendation
 
 

Sonidel Publication Search Results (9 results)

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[2010]

Lunatic fringe potentiates Notch signaling in the developing brain.
Kato TM, Kawaguchi A, Kosodo Y, Niwa H, Matsuzaki F.
Laboratory for Cell Asymmetry, Center for Developmental Biology, RIKEN Kobe Institute, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.
Mol Cell Neurosci., 45(1):12-25. Epub 2010 May 25. - Sep 2010
 

[2008]

Increasing the Cell Number of Host Tetraploid Embryos Can Improve the Production of Mice Derived from Embryonic Stem Cells
Hiroshi Ohta (E-mail: ohta@cdb.riken.jp), Yuko Sakaide , Kazuo Yamagata , and Teruhiko Wakayama
Laboratory for Genomic Reprogramming, Center for Developmental Biology, RIKEN, Kobe 650-0047, Japan
Biology of Reproduction, Volume 79, Issue 3, Pages 486–492 - September 2008
 
Apical Accumulation of Rho in the Neural Plate Is Important for Neural Plate Cell Shape Change and Neural Tube Formation
Nagatoki Kinoshita 1, Noriaki Sasai, Kazuyo Misaki 1 and Shigenobu Yonemura 1 (E-mail: yonemura@cdb.riken.jp)
1 Electron Microscope Laboratory and Organogenesis and Neurogenesis Group, RIKEN Center for Developmental Biology, Kobe 650-0047, Japan
Molecular Biology of the Cell, Volume 19, Issue 5, Pages 2289-2299 - May 2008
 
Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis
Daijiro Konno 1,4, Go Shioi 1,4, Atsunori Shitamukai 1, Asako Mori 1, Hiroshi Kiyonari 2, Takaki Miyata 3 & Fumio Matsuzaki 1 (E-mail: fumio@cdb.riken.jp)
1 Laboratory for Cell Asymmetry, Center for Developmental Biology, RIKEN, and CREST, Japan Science and Technology Corporation, RIKEN, 2-2-3 Minatojima-Minamimachi, Chuou-ku, Kobe 650-0047, Japan.
2 Laboratory for Animal Resources and Genetic Engineering, Center for Developmental Biology, RIKEN, 2-2-3 Minatojima-Minamimachi, Chuou-ku, Kobe 650-0047, Japan.
3 Department of Anatomy and Cell Biology, and CREST, Japan Science and Technology Corporation, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya, Aichi 466-8550, Japan.
4 These authors contributed equally to this work.
Nature Cell Biology, Volume10, Number 1, Pages 93-101 - January 2008
 

[2007]

Early Changes in KCC2 Phosphorylation in Response to Neuronal Stress Result in Functional Downregulation
Hiroaki Wake 1, 2, Miho Watanabe 1, Andrew J. Moorhouse 3, Takashi Kanematsu 4, Shoko Horibe 1, 6 Noriyuki Matsukawa 2, Kiyofumi Asai 5, Kosei Ojika 2, Masato Hirata 4 and Junichi Nabekura 1, 6, 7 (E-mail: nabekura@nips.ac.jp)
1 Division of Homeostatic Development, National Institute of Physiological Sciences, Okazaki 444-8585, Japan
2 Department of Neurology and Neuroscience, Nagoya City University Graduate School of Medical Sciences, Mizuho-ku, Nagoya 467-8601, Japan
3 Department of Physiology and Pharmacology, School of Medical Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia
4 Molecular and Cellular Biochemistry, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, Japan
5 Department of Molecular Neurobiology, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan
6 School of Life Science, The Graduate University for Advanced Studies, Hayama 240-0193, Japan
7 Core Research for the Evolutionary Science and Technology, Japan Science and Technology Corporation, Saitama 332-0012, Japan
The Journal of Neuroscience, Volume 27, Issue 7, Pages 1642-1650 - 14 February 2007
 
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