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Cells containing this marker were distributed throughout the trigeminal ganglion.
Enzymes, buffers and mass weight marker were from Fermentas, Thermo Scientific.
One thousand permutation tests per marker were run to determine a significant threshold.
The Gn1a-17 SNP marker and GS5-03 SNP marker were developed based on this method.
553989, clone A95-1), antibodiesies to the tested marker were used.
Known fluorescent proteins mCherry, and OsGenL-CFP (nuclear marker) were used as markers of localizations.
Carotenoid pigments from bacterial symbionts and β-carotene marker were dissolved in methanol at several concentrations.
The intensity and position of stains in epithelial tissue positive for this marker were also analyzed.
In addition, genes located in intervals of 50 kb on both sides of the marker were explored.
The restriction enzyme FastDigest AvaI, EcoRI, T4 DNA Ligase, DNA, and protein marker were purchased from Thermo Scientific.
The Plasmid DNA purification kit, DNA purification kit and DNA marker were purshased from GeneMark Technology (Tainan, Taiwan).
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