Evidence map›Paper›PMID 29430869›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2018

Monoclonal Cell Line Generation and CRISPR/Cas9 Manipulation via Single-Cell Electroporation.

Ruiguo Yang, Vincent Lemaître, Changjin Huang, Abbas Haddadi, Rebecca McNaughton, Horacio D Espinosa

Open access · greenAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Semi-Implantable Bioelectronics.Nano-micro letters · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Points of View on the Tools for Genome/Gene Editing.International journal of molecular sciences · 2021
    Review
  14. Microfluidic and Nanofluidic Intracellular Delivery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  15. [Rapid screening of single guide RNA targeting pig genome and the harvesting of monoclonal cells by microarray seal].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2021
    Article
  16. Nanoneedle-Based Materials for Intracellular Studies.Advances in experimental medicine and biology · 2021
    Article
  17. Review
  18. Review
  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

6 authors at 3 institutions in 1 country.

Ruiguo YangDepartment of Mechanical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Vincent LemaîtreiNfinitesimal LLC, Skokie, IL, 60077, USA.
Changjin HuangDepartment of Mechanical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Abbas HaddadiiNfinitesimal LLC, Skokie, IL, 60077, USA.
Rebecca McNaughtoniNfinitesimal LLC, Skokie, IL, 60077, USA.
Horacio D EspinosaDepartment of Mechanical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Infinitesimal (United States) · USNorthShore University HealthSystem · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1993 to 2026
$153.9M
A Force-controlled Probe Based Platform for Single-Cell Biomolecular DeliveryR44GM101833 · NIGMS · INFINITESIMAL, LLC · PI LEMAITRE, VINCENT · 2015 to 2016
$1000k
FACSAria SORP Cell SorterS10OD011996 · OD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOOLSBY, CHARLES L. · 2012 to 2012
$482k
NCI NIH HHS P30 CA060553NIGMS NIH HHS R44 GM101833NIH HHS S10 OD011996
6 · The paper itself

Abstract

Stably transfected cell lines are widely used in drug discovery and biological research to produce recombinant proteins. Generation of these cell lines requires the isolation of multiple clones, using time-consuming dilution methods, to evaluate the expression levels of the gene of interest. A new and efficient method is described for the generation of monoclonal cell lines, without the need for dilution cloning. In this new method, arrays of patterned cell colonies and single cell transfection are employed to deliver a plasmid coding for a reporter gene and conferring resistance to an antibiotic. Using a nanofountain probe electroporation system, probe positioning is achieved through a micromanipulator with sub-micron resolution and resistance-based feedback control. The array of patterned cell colonies allows for rapid selection of numerous stably transfected clonal cell lines located on the same culture well, conferring a significant advantage over slower and labor-intensive traditional methods. In addition to plasmid integration, this methodology can be seamlessly combined with CRISPR/Cas9 gene editing, paving the way for advanced cell engineering.

Indexed as

AnimalsCell LineCRISPR-Cas SystemsElectroporationGene EditingHumansPlasmidsTransfectioncell line generationelectroporationnanofountain probesingle cell

Identifiers

PMID29430869
PMCPMC6016377
OpenAlexW2789803765

What OpenQuestion holds

Textmetadata
LicenceTDM
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.