Finally, we successfully established a pair of ternatin molecular probes.
By a crossing strategy, we successfully established stable Orco mutant lines.
Further, we successfully established a correlation to quantify the influence of these process variables of the freeze-gelation method on the tensile properties of the scaffolds.
In our previous studies, we successfully established the conversion of glycerol to ethanol by overexpression of pGcyaDak with pGup1Cas in Saccharomyces cerevisiae.
We successfully established the expression systems for (1) and (3), and succeeded in purification of the soluble FDHs with a tag by using affinity columns.
In this study, we successfully established an additive-free microwave hydrothermal (M-H) route by only using Al2 SO4 3 aqueous solution and urea as raw materials.
We successfully established miR-33b knock-in (KI) mice and found that protein levels of known miR-33a target genes, such as ABCA1, ABCG1, and SREBP-1, were reduced compared with those in wild-type mice.
In conclusion, we successfully established that the co-expression of SPT3 and SPT15 that improved the fermentation performance of the engineered yeast strains which produced higher ethanol yields than stress-sensitive yeast strains.
Besides, by integration of the microfilter and a LAMP chip on a portable device, we successfully established a point-of-care system for enrichment and analysis of airborne pathogens.
In this study, we successfully established six homozygous MHC-B haplotype populations from the BWEL chickens using microsatellite marker technology, named as BW/G 1, 2, 3, 5, 6, 7) lines, and their molecular genotypes were matched to six serologically defined MHC-B haplotypes, B13, B15, B2, B5, B21 and B19, respectively.
We successfully established a site-specific transgenic system with comparable transformation efficiency to transposon-based genetic transformation through microinjection of TALENs mRNA targeting the BmBLOS2 locus and a linearizable donor plasmid encoding an expression cassette of the DsRed2 red fluorescent protein.
