Evidence map›Paper›PMID 42108346›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Laboratory-Scale Production of Recombinant IgG Antibodies.

Takahiro Anzai, Masahiro Yasunaga

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Takahiro AnzaiDepartment of Chemistry and Materials Science, National Institute of Technology (KOSEN), Gunma College, Maebashi, Gunma, 370-8531, Japan. tak-anzai@umin.ac.jp.
Masahiro YasunagaDivision of Developmental Therapeutics, EPOC, National Cancer Center, Kashiwa, Chiba, 277-8577, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of hybridoma technology by Köhler and Milstein revolutionized the field of antibody research, paving the way for the creation of monoclonal antibodies. Due to their ability to specifically bind target molecules via antigen-antibody reactions, antibodies have become a major focus in therapeutic development. However, antibodies obtained from immunized animals such as mice may cause immunogenicity or side effects when administered to humans. While humanized mice offer a solution, their high-cost limits widespread adoption. Advances in genetic engineering technology have made it possible to create chimeric antibodies or humanized antibodies and have greatly reduced immunogenicity. In this chapter, we explain in detail a laboratory-scale protocol to produce recombinant IgG antibodies at the milligram scale, which is essential for in vivo research, using transient expression in CHO cells.

Indexed as

Antibodies, MonoclonalImmunoglobulin GRecombinant ProteinsAnimalsCHO CellsCricetinaeCricetulusHumansMiceProtein EngineeringAntibodies, MonoclonalImmunoglobulin GRecombinant ProteinsAnimal studyAntibody engineeringAntibody productionCHO cellsIgG antibodyMilligram-scaleMonoclonal antibodyRecombinant antibodyTransient expression

Identifiers

What OpenQuestion holds

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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.