sample review
  • Anti-p62 antibody was used for immunohistochemical staining, in order to study the mechanism by which MAPKAPK2/MAPKAPK3 activate starvation-induced autophagy.
  • Abcam anti-CK18 antibody was used to perform immunofluorescence in order to study the compementary roles of Grb10 in mother and pun during the developmental programming.
  • Progen Biotechnik mouse anti-Desmoplakin 1/2 (2.15) was used to perform western blot in order to study the role for TRAF4, a novel phosphoinositide-binding protein in modulating tight junctions and promoting cell migration.
  • Progen Biotechnik GmbH anti-VCP/p97 monoclonal antibody was used to perform Western Blot in order to study the possible role of VCP/p97 in myelomonocytic differentiation and retrodifferentiation.
  • Progen p62 antibody (Gp62-C) was used to perform western blot in order to describe important roles for autophagy in the maintenance of balance such as inner ear development and equilibrioception.
  • Progen mouse monoclonal anti-lamin B2 antibody was used in western blot in order to investigate the effects of the expression of human LBR disease mutants on cellular structure.
  • Progen anti-synaptophysin monoclonal antibody was used in immunocytochemistry in order to investigate the mechanism for the paracrine role of GABA in rat adrenal medullary (AM) cells at the molecular level.
  • PROGEN Biotechnik GmbH guinea pig anti-p62 antibody was used in western blot in order to demonstrate that efficient autophagic degradation of protein aggregates associated with neurodegenerative disease requires functional multivesicular bodies (MVBs).
  • Progen anti-p62 antibody was used to perform immunohistochemistry in order to study the effect after the loss of the ALS2/Alsin in a SOD1H46R-expressing mouse ALS model.
  • BD-Pharmingen Bax antibody was used in western blot in order to study the consequences of Bax silencing on autophagic vs. apoptotic responses to Bcl-2 inactivation.
  • Progen Biotechnik polyclonal guinea pig anti-nephrin antibody was used in western blot in order to demonstrate cultured human podocytes express the CCR2 receptor and the MCP-1/CCR2 system can induce a migratory response in this cell type.