Exact(2)
Exon-intron organization was determined using the genome browser in RAP-DB (http://rapdb.dna.affrc.go.jp/).jp/
Scans for the active sites of OsATG homologues were performed using PROSITE (http://www.expasy.ch/tools/scanprosite/). Exon intron organization was determined using the genome browser tool in RAP-DB.
Similar(56)
The genomic organization of rat urocortin was determined using both cDNA and liver genomic DNA as templates for polymerase chain reactions.
The genomic organization of each gene was determined using two methods.
The exon-intron organization of V regions was determined using sequences obtained by 5' RACE.
In addition, the intracellular organization of F-actin was determined using fluorescently labeled phalloidin, because it has been known that F-actin undergoes structural remodeling to localize to the peri-plasma membrane region, where it can stabilize AJ [ 18].
In addition, three-dimensional collagen fiber organization of the rabbit cornea was determined using nonlinear optical high-resolution macroscopy.
SRCR domain organization of alternatively spliced variants was determined using ClustalW2 analysis of deduced amino acid sequences to determine which domains were represented in each clone.
The growth and differentiation of individual cell types was determined using live cell fluorescent microscopy demonstrating the utility of fluorescent labels to monitor tissue organization in real time.
Peptide binding was determined using ELISA.
Iodine uptake was determined using radioactive iodine.
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