Evidence map›Paper›PMID 40395840›Full record

ArticleBio-protocol2025

PCR-Based Genotyping of Zebrafish Genetic Mutants.

Swathy Babu, Yuko Nishiwaki, Ichiro Masai

Abstract read
In one paragraph

Article in Bio-protocol, 2025. 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

3 authors.

Swathy BabuDevelopmental neurobiology unit, Okinawa Institute of Science and Technology Graduate University, Onna, Japan.
Yuko NishiwakiDevelopmental neurobiology unit, Okinawa Institute of Science and Technology Graduate University, Onna, Japan.
Ichiro MasaiDevelopmental neurobiology unit, Okinawa Institute of Science and Technology Graduate University, Onna, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zebrafish genetic mutants have emerged as a valuable model system for studying various aspects of disease and developmental biology. Mutant zebrafish embryos are generally identified based on phenotypic defects at later developmental stages, making it difficult to investigate underlying molecular mechanisms at earlier stages. This protocol presents a PCR-based genotyping method that enables the identification of wild-type, heterozygous, and homozygous zebrafish genetic mutants at any developmental stage, even when they are phenotypically indistinguishable. The approach involves the amplification of specific genomic regions using carefully designed primers, followed by gel electrophoresis. This genotyping method facilitates the investigation of the molecular mechanisms driving phenotypic defects that are observed at later timepoints. This protocol allows researchers to perform analyses such as immunofluorescence, RT-PCR, RNA sequencing, and other molecular experiments on early developmental stages of mutants. The availability of this protocol expands the utility of zebrafish genetic mutants for elucidating the molecular underpinnings of various biological processes throughout development. Key features • Enables genotyping of zebrafish genetic mutants at any developmental stage, even before the onset of phenotypic defects. • Utilizes PCR amplification and restriction enzyme digestion to distinguish wild-type, mutant, and heterozygous genotypes.

Indexed as

Developmental biologyEmbryosGenotypingModel organismMutant analysisPCRPhenotypic defectsRestriction enzyme digestionZebrafish

Identifiers

PMID40395840
PMCPMC12086339

What OpenQuestion holds

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Registered trials

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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.