Literature DB >> 2458952

Single cell assay with an automated capillary microinjection system.

R Pepperkok1, C Schneider, L Philipson, W Ansorge.   

Abstract

An automated capillary microinjection system with computer-controlled positioning of the cells and of the capillary, and its applications and advantages, is described. The system is easy in handling and manipulation. About 1500 injections are possible in 1 h, with high reproducibility. In cytoplasmic and nuclear injections more than 90 and 85% of the cells are successfully injected. Using FITC-dextran at a concentration of 0.5% as a fluorescently labeled coinjection marker, 99% of the cells can be retrieved in culture medium even 48 h after injection. The coordinates of the cells are stored in the computer and accuracy in statistical evaluation of experiments is improved in comparison to the manual techniques. Methods for preparation and handling of glass capillaries were developed resulting in reproducible form and significantly reduced clogging rate. The improved characteristics offered by this system are demonstrated in studies leading to the confirmation of existence of an mRNA inhibiting DNA synthesis in cells. Functional screening by cell injections of cDNA libraries and of size-fractionated mRNA molecules can be performed efficiently with the automated microinjection system.

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Year:  1988        PMID: 2458952     DOI: 10.1016/0014-4827(88)90406-5

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  17 in total

1.  Single cell assay with an automated capillary microinjection system.

Authors:  R Pepperkok; C Schneider; L Philipson; W Ansorgel
Journal:  Cytotechnology       Date:  1991-02       Impact factor: 2.058

2.  Transfer of macromolecules into living adult cardiomyocytes by microinjection.

Authors:  M Bartoli; W C Claycomb
Journal:  Mol Cell Biochem       Date:  1997-07       Impact factor: 3.396

3.  The jun and fos protein families are both required for cell cycle progression in fibroblasts.

Authors:  K Kovary; R Bravo
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

4.  Delivery of proteases in aqueous two-phase systems enables direct purification of stem cell colonies from feeder cell co-cultures for differentiation into functional cardiomyocytes.

Authors:  John P Frampton; Huilin Shi; Albert Kao; Jack M Parent; Shuichi Takayama
Journal:  Adv Healthc Mater       Date:  2013-04-17       Impact factor: 9.933

5.  Existence of different Fos/Jun complexes during the G0-to-G1 transition and during exponential growth in mouse fibroblasts: differential role of Fos proteins.

Authors:  K Kovary; R Bravo
Journal:  Mol Cell Biol       Date:  1992-11       Impact factor: 4.272

6.  Human cyclin E, a nuclear protein essential for the G1-to-S phase transition.

Authors:  M Ohtsubo; A M Theodoras; J Schumacher; J M Roberts; M Pagano
Journal:  Mol Cell Biol       Date:  1995-05       Impact factor: 4.272

7.  Prohibitin, an evolutionarily conserved intracellular protein that blocks DNA synthesis in normal fibroblasts and HeLa cells.

Authors:  M J Nuell; D A Stewart; L Walker; V Friedman; C M Wood; G A Owens; J R Smith; E L Schneider; R Dell' Orco; C K Lumpkin
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

8.  The cytoplasmic domain of alphavirus E2 glycoprotein contains a short linear recognition signal required for viral budding.

Authors:  M Kail; M Hollinshead; W Ansorge; R Pepperkok; R Frank; G Griffiths; D Vaux
Journal:  EMBO J       Date:  1991-09       Impact factor: 11.598

9.  Cyclin A is required at two points in the human cell cycle.

Authors:  M Pagano; R Pepperkok; F Verde; W Ansorge; G Draetta
Journal:  EMBO J       Date:  1992-03       Impact factor: 11.598

10.  Microfilament reorganization during apoptosis: the role of Gas2, a possible substrate for ICE-like proteases.

Authors:  C Brancolini; M Benedetti; C Schneider
Journal:  EMBO J       Date:  1995-11-01       Impact factor: 11.598

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