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In order to prove expression of SCN8A protein in cardiomyocytes, we were able to detect SCN8A protein in rat cardiomyocytes of different developmental stages by means of immunocytochemistry.
To prove expression of Dxr in the apicoplast, polyclonal antibodies were raised against recombinant PfDxr (Figure 2 and Figure S11) and antibody staining was performed on intracellular T. gondii tachyzoites and P. falciparum blood stages.
Genomic approaches, such as SAGE and DNA microarrays, do not prove expression at the protein level.
The availability of RNA sequencing (RNA-Seq) data from whole body or specific tissues can be valuable to prove expression of particular genes.
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It proved expression protein to be a recombinant fusion protein with 6 His tag.
We were able to prove gene expression of such transporters for both, nitrogen and sulfate starvation as well as the increased expression for other nitrogen and sulfate specific genes.
We can prove the expression of the smoothing parameter using MISE method.
In the present study, we were able to prove the expression of brain-type VGSC in the developing rat myocardium.
Our experiments finally prove the expression of OATP1C1 in subpopulations of astrocytes.
In this Appendix, we prove an expression (9) for the probability of transmission across a given link.
In order to prove the expression of a protein, we required two discriminating peptides or discriminating peptides from two or more analyses.
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