sample review
  • Mx3000P machine was used for quantitative RT-PCR, in order to study the heritable capture of heterochromatin dynamics in Saccharomyces cerevisiae
  • function generator was used for immunohistochemistry, in order to demonstrate optogenetics as a useful tool for controlling fertilization and cAMP signaling in sperm.
  • Anti-FLAG antibody was used for immunoassay, in order to study the role of GTPase Rab26 in directing synaptic and secretory vesicles into the autophagy pathway.
  • pCMV-Tag2a was used for DNA recommendation, in order to study the role of GTPase Rab26 in directing synaptic and secretory vesicles into the autophagy pathway.
  • QuickChange site mutagenesis kit was used to construct mutation, in order to study the mechanism by which MAPKAPK2/MAPKAPK3 activate starvation-induced autophagy.
  • Site-Directed Mutagenesis kit was used for DNA mutation, in order to study the mechanism by which Cry1/2 protect genomic integrity.
  • Pfu turbo DNA polymerase was used in order to investigate the mechanism by which G-actin tunes the integrated stress response
  • Monolithic laser combiner was used for confocal microscopy analysis in order to study the effects of aneuploidy on chromosome mis-segregation and cytokinesis failure.
  • AffinityScript multiple temperature cDNA synthesis kit was used in qRT-PCR in order to analyze expression of genes that involved in regulatory pathways in Candida albicans during mammalian infection.
  • QuikChange XL was used to construct mutation in order to study the mechanism that how the Mms21 SUMO Ligase is controlled during DNA Repair.
  • Agilent Technologies BL21 (DE3) CodonPlus-RIPL Escherichia coli strain was used to perform protein expression in order to study therole of the human lariat RNA debranching enzyme 1 protein in both the nucleus and the cytoplasm.