sample review
  • Anti-Atg16L1 antibody was used for immunoassay, in order to study the role of GTPase Rab26 in directing synaptic and secretory vesicles into the autophagy pathway.
  • Anti-Flag antibody was used in order to study the role of a cascade consisting of GSK3beta, Dzip1, and Rab8 in regulating ciliogenesis after mitosis.
  • Anti-GFP antibody was used in order to study the role of a cascade consisting of GSK3beta, Dzip1, and Rab8 in regulating ciliogenesis after mitosis.
  • MBL anti-beta-actin was used to perform western blot in order to study therole of the human lariat RNA debranching enzyme 1 protein in both the nucleus and the cytoplasm.
  • MBL International anti-phospho-vimentin 4A4 was used to perform immunohistochemistry in order to study the function of NDE1 in S phase of early neural progenitor differentiation.
  • MBL International rabbit anti-GFP was used to perform immunohistochemistry in order to study the regulation of the Teneurins on Synaptic organization of the Drosophila antennal lobe.
  • MBL rabbit anti-HA was used to perform western blot in order to study the role of Smurf proteins in controlling Hh signaling.
  • MBL mouse anti-Myc was used to perform western blot in order to study the role of Smurf proteins in controlling Hh signaling.
  • MBL anti-p21 antibody was used to perform western blotting in order to study JMJD6 promotes colon carcinogenesis through negative regulation of p53.
  • MBL anti-p53 antibody was used to perform western blotting in order to study JMJD6 promotes colon carcinogenesis through negative regulation of p53.
  • MBL rabbit anti-RFP antibody was used to perform western blot in order to investigate the structural composition of caveolar coat complex.