The HPT (hygromycin) marker was used for selection of homozygous plants.
A wide range molecular weight marker was used to estimate the molecular weight.
The marker was used to obtain ground truth using optical tracking.
The same volume of 3 μl of molecular weight marker was used in every gel.
As protein ladder a 10 250 kDa prestained marker was used (ThermoFisher, USA).
A semi-quantitative ELISA kit, which detects glial fibrillary acidic protein (GFAP) as marker, was used.
The marker was used to detect the F2, BC1, and F2 3 populations.
Biotin-conjugated protein marker was used for the purpose of both molecular weight ladders and positive controls.
Moreover, 131I, a radioactive marker, was used to radiolabel the PLGA-lipid nanoparticles to clearly assess their in vivo behavior.
Uncontrolled mycelia growth that led to clogging of the TBR was observed when fungus without a pyridoxine marker was used for XynB production.
An inducible origin of replication linked with an antibiotic resistance marker was used as a cassette for targeted replacement of sequences within a HCMV BAC clone, TowneBAC.
