Literature DB >> 8069452

Cell lines used for the selection of recombinant baculovirus.

J E Maruniak1, A Garcia-Canedo, J J Rodrigues.   

Abstract

Four insect cell lines were used to isolate two recombinant baculoviruses which had the beta-galactosidase (beta-gal) gene for colorimetric assay purposes. Plaque assays were performed using two Trichoplusia ni cell lines: BTI-TN-5B1-4 and TN-368, and two Spodptera frugiperda cell lines: IPLB-SF-21AE and SF9. The number of plaques (occlusion positive and blue beta-gal+ recombinants) formed in the Trichoplusia cells was higher than in the Spodoptera cells. The appearance of Autographa californica NPV polyhedra was also faster in the T. ni cell lines. The effect of cell passage on the plaque formation proved to be critical when two different passages of the SF9 cells were tested. The higher passage produced a lower viral titration. The size and time of appearance of the plaques was also different.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8069452     DOI: 10.1007/bf02632053

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol Anim        ISSN: 1071-2690            Impact factor:   2.416


  17 in total

1.  Nuclear polyhedrosis virus detection: relative capabilities of clones developed from Trichoplusia ni ovarian cell line TN-368 to serve as indicator cells in a plaque assay.

Authors:  L E Volkman; M D Summers
Journal:  J Virol       Date:  1975-12       Impact factor: 5.103

Review 2.  Expression of eukaryotic genes in insect cultures.

Authors:  M J Fraser
Journal:  In Vitro Cell Dev Biol       Date:  1989-03

3.  Analysis of baculovirus genomes with restriction endonucleases.

Authors:  G E Smith; M D Summers
Journal:  Virology       Date:  1978-09       Impact factor: 3.616

4.  An improved method for visualizing baculovirus plaques in cell agarose overlays.

Authors:  A B Shanafelt
Journal:  Biotechniques       Date:  1991-09       Impact factor: 1.993

5.  In vivo and in vitro host range of Autographa californica nuclear polyhedrosis virus and Spodoptera frugiperda nuclear polyhedrosis virus.

Authors:  G M Danyluk; J E Maruniak
Journal:  J Invertebr Pathol       Date:  1987-11       Impact factor: 2.841

6.  Plaque assay of baculoviruses employing an agarose-nutrient overlay.

Authors:  D L Knudson
Journal:  Intervirology       Date:  1979       Impact factor: 1.763

7.  Established insect cell line from the cabbage looper, Trichoplusia ni.

Authors:  W F Hink
Journal:  Nature       Date:  1970-05-02       Impact factor: 49.962

8.  Efficient, low-cost protein factories: expression of human adenosine deaminase in baculovirus-infected insect larvae.

Authors:  J A Medin; L Hunt; K Gathy; R K Evans; M S Coleman
Journal:  Proc Natl Acad Sci U S A       Date:  1990-04       Impact factor: 11.205

9.  Strong and regulated expression of Escherichia coli beta-galactosidase in insect cells with a baculovirus vector.

Authors:  G D Pennock; C Shoemaker; L K Miller
Journal:  Mol Cell Biol       Date:  1984-03       Impact factor: 4.272

10.  The expression of hemolytically active human complement protein C9 in mammalian, insect, and yeast cells.

Authors:  S Tomlinson; E Ueda; J E Maruniak; A Garcia-Canedo; E S Bjes; A F Esser
Journal:  Protein Expr Purif       Date:  1993-04       Impact factor: 1.650

View more
  2 in total

1.  Productivity of insect cells for recombinant proteins.

Authors:  J E Maruniak
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

2.  Efficient production of foot-and-mouth disease virus empty capsids in insect cells following down regulation of 3C protease activity.

Authors:  Claudine Porta; Xiaodong Xu; Silvia Loureiro; Saravanan Paramasivam; Junyuan Ren; Tara Al-Khalil; Alison Burman; Terry Jackson; Graham J Belsham; Stephen Curry; George P Lomonossoff; Satya Parida; David Paton; Yanmin Li; Ginette Wilsden; Nigel Ferris; Ray Owens; Abhay Kotecha; Elizabeth Fry; David I Stuart; Bryan Charleston; Ian M Jones
Journal:  J Virol Methods       Date:  2012-11-19       Impact factor: 2.014

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.