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The RT-PCR products were run on 1.5% agarose gels containing 0.1 mg/ml ethidium bromide, and were visualised using the Bio Profile software (LTF, Wasserburg, Germany).
The RT-PCR products were electrophoretically separated on 1.5% agarose gels containing 0.1 mg/ml ethidium bromide and visualised using Bio Profile software (LTF), allowing correlation between EF-1α signals and cycle number for each sample.
The RT-PCR products were electrophoretically separated on 1.5% agarose gels containing 0.1 mg/mL ethidium bromide and visualized using the Bio Profile software (LTF, Wasserburg, Germany), allowing correlation between EF1α signals and cycle number for each sample.
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The densities of the enzyme bands were determined by the BioCapt and Bio-Profile (Bio-1D) software.
The radioactive PIP signals were quantitated via densitometry using the Bio-profile Bio-1D application (Vilber-Lourmat, France) [ 23].
Densitometric analysis was conducted using the Bio-profile Bio-ID application (Vilber-Lourmat, Marne-la-Vallée, France).
Bands corresponding to each specific PCR product were quantified via the densitometric scanning of the exposed film using the Bio-profile Bio-ID application.
The relative abundance of each protein was quantified by using the Bio-profile Bio-1D application (Vilber-Lourmat), and the expression levels were normalized to the control protein.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com