Evidence map›Paper›PMID 30174558›Full record

ArticleJournal of biomolecular techniques : JBT2018

Cytosolic and Transmembrane Protein Extraction Methods of Breast and Ovarian Cancer Cells: A Comparative Study.

Thingreila Muinao, Mintu Pal, Hari Prasanna Deka Boruah

Open access · diamondAbstract readComparative Study
In one paragraph

Article in Journal of biomolecular techniques : JBT, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. On-Demand Proximity Labeling Using Light-Activated BioID.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  6. Deletion of SUMO1 attenuates behavioral and anatomical deficits by regulating autophagic activities in Huntington disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Parasitology · 2020
    Article
  9. 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

3 authors at 2 institutions in 1 country.

Thingreila MuinaoBiological Sciences and Technology Division, Biotechnology Group, Council of Scientific and Industrial Research-North East Institute of Science and Technology, Academy of Scientific and Innovative Research, Jorhat, Assam, India.
Mintu PalBiological Sciences and Technology Division, Biotechnology Group, Council of Scientific and Industrial Research-North East Institute of Science and Technology, Academy of Scientific and Innovative Research, Jorhat, Assam, India.
Hari Prasanna Deka BoruahBiological Sciences and Technology Division, Biotechnology Group, Council of Scientific and Industrial Research-North East Institute of Science and Technology, Academy of Scientific and Innovative Research, Jorhat, Assam, India.
North East Institute of Science and Technology · INAcademy of Scientific and Innovative Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient extraction of proteins is a great challenge for numerous downstream proteomic analyses. During the protein extraction procedure, it is critical to maintain the conformational stability, integrity, as well as higher yield of the protein. To do so, 5-different lysis buffers of Tris and HEPES have been used as the primary buffering reagents with variable compositions at different concentrations and pH using human cancer cells. In this study, different protein lysates of human breast cancer cells T47D and MDA-MB-231 and ovarian cancer cell PA-1 were subjected to run SDS-PAGE for separation of proteins based on their molecular size, followed by Coomassie blue, silver staining, and immunoblot assays to compare the extraction yield of total cytoplasmic proteins, glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the integral membrane protein, integrin β-1. Our results revealed that Tris-based lysis buffer with 50 mM concentration, pH 7.5, is relatively the efficient and reliable protein extraction method for a wide range of MW subcellular markers, cytoplasmic GAPDH and transmembrane integrin β-1 proteins. We anticipate that this simple and cost-effective protein extraction protocol might be extremely useful across a broad range of subcellular proteins in different biologic samples.

Indexed as

Breast NeoplasmsBuffersCell Line, TumorCytosolElectrophoresis, Polyacrylamide GelFemaleGlyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)HumansImmunoblottingIntegrin beta1Membrane ProteinsMolecular BiologyNeoplasm ProteinsOvarian NeoplasmsBuffersGlyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)Integrin beta1Membrane ProteinsNeoplasm ProteinsCoomassie blueimmunoblotSDS-PAGEsilver staining

Identifiers

PMID30174558
PMCPMC6091320
OpenAlexW2892333029

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.