Evidence map›Paper›PMID 16211514›Full record

ArticleJournal of structural and functional genomics2005

Large-scale transient transfection of mammalian cells: a newly emerging attractive option for recombinant protein production.

Sabine Geisse, Mario Henke

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of structural and functional genomics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Article
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  3. Review
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  6. Article
  7. Functional Analysis of the 3' Untranslated Region of the HumanNeuropsychiatric disease and treatment · 2020
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  12. Review
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  14. Review
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  16. Article
  17. Expression of recombinant antibodies.Frontiers in immunology · 2013
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Sabine GeisseNovartis Institutes for BioMedical Research, Discovery Technologies/Biomolecules Production, 4002, Basel, Switzerland. Sabine.Geisse@novartis.com
Mario Henke

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammalian expression systems have an undisputed long-standing and very successful history for the generation of recombinant proteins, mainly as biopharmaceuticals. However, for use as 'tool proteins' in, e.g. assay development and screening, for structure elucidation and as antigens these expression systems were generally regarded as being cumbersome, tedious and expensive. This bias has largely been overcome with the very recent development of large-scale transient transfection (LST) approaches. Especially the HEK.EBNA expression system described here has contributed significantly to this success. The simplicity and speed of this approach compares well with expression trials using the widely applied Baculovirus/insect cell system. In addition, proteins generated in mammalian cells are usually correctly folded, fully processed and functionally active.

Indexed as

BioreactorsCell LineCulture MediaEpstein-Barr Virus Nuclear AntigensHumansRecombinant ProteinsTransfectionCulture MediaEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensRecombinant Proteins

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.