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| Method to introduce foreign DNA into host cells by electric pulse interruption of host cell's phospholipid bilayer membrane. |
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Single-Cell Electroporation Protocol
new recommended
protocol
A single-cell electroporation protocol for recombinant DNA transferation developed in Hollis Cline's lab at Cold Spring Harbor Laboratory.
This technique utilizes electroporation in which a brief external high voltage pulse induces sufficient transmembrane ...
Problems of electroporation
troubleshooting
Does anyone have experience of successful
transformation of control plasmid into E. coli with
electroporator, but nothing resulted with ligated DNA
(after ethanol precipitation)??
... ...
...
Gene-gun transfection of hippocampal neurons video
media
Gene-gun transfection of hippocampal neurons
Powrnima Joshi, Anna Dunaevsky
Brown University
...
Transfection by electroporation. (Curr Protoc Cell Biol. 2003 Aug;Chapter 20:Unit 20.5.) Potter H.
Harvard Medical School, Boston, Massachusetts, USA.
Electroporation-the use of high-voltage electric shocks to introduce DNA into cells-can be used with most cell types, yields a high frequency of both stable transformation and transient gene expression, and, because it requires fewer steps, can be easier than alternate techniques. In this unit, the basic protocol describes the electroporation of mammalian cells and an alternate protocol outlines modifications for preparation and transfection of plant protoplasts.
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Last update: 17-May-2008 01:27 am
Related new papers and reviews
NONINVASIVE TRANSCUTANEOUS SAMPLING OF GLUCOSE BY ELECTROPORATION. J Diabetes Sci Technol. 2008;2(3):250-254 Authors: Srinivasa Murthy S, Siva Ram Kiran V, Mathur S, Narasimha Murthy S
BACKGROUND: In people with diabetes, blood glucose levels should be regularly monitored to prevent serious complications associated with diabetes. This involves invasive method of withdrawing blood which causes inconvenience to patients. The objective of the study was to investigate the efficiency of noninvasive Electroporation and Transcutaneous Sampling (ETS) technique for predicting blood glucose levels. METHODS: In vitro studies were carried out in Franz diffusion cells using porcine epidermis to assess the feasibility of transcutaneous sampling of glucose. In vivo, the ETS technique was assessed in diabetes induced sprague dawley rat model. Glucose was sampled following the application of 30 electrical pulses of 1ms duration at 120 V/cm(2), 1 Hz. Clarke Error Grid Analysis was carried out for the venous blood glucose levels that were determined by ETS with reference to that measured by glucose meter. RESULTS: The amount of glucose sampled by the ETS method in both in vitro and in vivo was proportional to the dermal glucose concentration. All the data points from in vivo studies were in A and B zones of Clarke error grid analysis and the mean absolute relative error was found to be 12.8%. CONCLUSIONS: The results of the present study demonstrate that ETS technique could be developed as a noninvasive method of predicting venous blood glucose levels in diabetics.
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