Evidence map›Paper›PMID 32661464›Full record

ArticleAnalytical methods : advancing methods and applications2020

Fast Immunoassay for Microfluidic Western Blotting by Direct Deposition of Reagents onto Capture Membrane.

Natalie E Arvin, Mohamed Dawod, Don T Lamb, Jon P Anderson, Michael D Furtaw, Robert T Kennedy

Open access · greenAbstract read
In one paragraph

Article in Analytical methods : advancing methods and applications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Microfluidics for Peptidomics, Proteomics, and Cell Analysis.Nanomaterials (Basel, Switzerland) · 2021
    Review
  6. Review
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.

Natalie E ArvinDepartment of Chemistry, University of Michigan, 930 N. University Ave., Ann Arbor, Michigan 48109, United States.ORCID 0000-0002-5765-6380
Mohamed DawodDepartment of Chemistry, University of Michigan, 930 N. University Ave., Ann Arbor, Michigan 48109, United States.
Don T LambLI-COR Biosciences, 4647 Superior St., Lincoln, Nebraska 68504, United States.
Jon P AndersonLI-COR Biosciences, 4647 Superior St., Lincoln, Nebraska 68504, United States.
Michael D FurtawLI-COR Biosciences, 4647 Superior St., Lincoln, Nebraska 68504, United States.
Robert T KennedyDepartment of Chemistry, University of Michigan, 930 N. University Ave., Ann Arbor, Michigan 48109, United States.
LI-COR Biosciences (United States) · USUniversity of Michigan · USUnited States Military Academy · US

Funding

MICROELECTRODE AND MICRODIALYSIS-BASED INSULIN SENSORSR01DK046960 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 1993 to 2020
$3.3M
Design and Use of Methods for Peptide Secretion Studies - Diversity SupplementR37DK046960 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2006 to 2015
$3.0M
Next Generation Western for high-throughput and high-content protein analysisR44GM112289 · NIGMS · LI-COR BIOSCIENCES, INC. · PI FURTAW, MICHAEL D · 2017 to 2019
$1.5M
Next Generation Western for high-throughput and high-content protein analysisR43GM112289 · NIGMS · LI-COR BIOSCIENCES, INC. · PI FURTAW, MICHAEL D · 2014 to 2015
$521k
NIDDK NIH HHS R01 DK046960NIDDK NIH HHS R37 DK046960NIGMS NIH HHS R43 GM112289NIGMS NIH HHS R44 GM112289
6 · The paper itself

Abstract

Western blotting is a widely used protein assay platform, but the technique requires long analysis times and multiple manual steps. Microfluidic systems are currently being explored for increased automation and reduction of analysis times, sample volumes, and reagent consumption for western blots. Previous work has demonstrated that proteins separated by microchip electrophoresis can be captured on membranes by dragging the microchip outlet across the membrane. This process reduces the separation and transfer time of a western blot to a few minutes. To further improve the speed and miniaturization of a complete western blot, a microscale immunoassay with direct deposition of immunoassay reagents has been developed. Flow deposition of antibodies is used to overcome diffusion limited binding kinetics so that the entire immunoassay can be completed in 1 h with detection sensitivity comparable to incubation steps requiring 20 h. The use of low microliter/min flow rates with antibody reagents applied directly and locally to the membrane where the target proteins have been captured, reduced antibody consumption ~30-fold. The complete western blot was applied to the detection of GAPDH and β-Tubulin from A431 cell lysate.

Indexed as

Electrophoresis, MicrochipMicrofluidicsBlotting, WesternImmunoassayIndicators and ReagentsIndicators and Reagentsimmunoassaymicrochip electrophoresismicrofluidicproteinsWestern blot

Identifiers

PMID32661464
PMCPMC7357712
OpenAlexW3010293320

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.