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In the third phase of selective coding, the core categories on which the interpretation of the group discussions was constructed were then worked out.
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This construct was then shuttled in different expression vectors.
The construct was then placed in a bioreactor.
This construct was then evaluated as a potential DNA vaccine.
The biomaterial-cell construct is then implanted into the zone to be treated.
This construct was then used in the generation of a recombinant NDV expressing CAT protein.
The construct was then lipofected into mesenchymal progenitor cells isolated from human bone marrow.
The radial construct was then stabilized with two Kirchner (K) wires, inserted from the radial styloid.
That construct is then tested under axial and torsion loads, with motion measured across the gap.
The construct was then cloned into pUAST.
The mutagenesis construct was then transferred to pDM4.
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