For each sample the orientation is checked against the current state's transition interval, and if the orientation value lies within that same interval the state is changed, otherwise the state remains the same.
Utilizing an internal PvuII restriction enzyme site orientation of promoter was checked and both sense and antisense constructs were selected for further experiments.
The position and orientation of the screws was checked with fluoroscopy.
Orientation of the sequences was checked using program OrientationChecker v.1.0 available at.
The correct orientation of the fragments was checked by control restriction digests.
For each genus, sequence orientation of all sequences was checked using BLASTN (19) and redundancy was eliminated using BLASTCLUST (19).
The orientation of the insert was checked, and a sense and an antisense version of the resulting recombinant intermediate plasmid were digested with PstI enzyme.
After transformation, the orientation of the insert was checked by restriction digestion and the correct clone was sent to Transgenic Fly Facility (TFF, C-CAMP, Bangalore) for generating transgenic lines.
The nanorod length was determined by observing the cross-section with a scanning electron microscope (JEOL JSM-6700F), while the crystallographic orientation of the nanorod was checked by measuring X-ray diffraction (XRD) pattern on a Rigaku SmartLab.
The molecular orientation in the grown nanostructures was checked by polarization-dependent optical measurements.
