sample review
  • Anti-p62 antibody was used for Western blotting, in order to study the mechanism by which MAPKAPK2/MAPKAPK3 activate starvation-induced autophagy.
  • Abnova anti-LDHB mouse monoclonal antibodies were used to perform immunocytochemistry in order to study the generation mechanism of Peroxisomal lactate dehydrogenase in mammals.
  • Abnova mouse anti-arfrp1 was used to perform western blot in order to identify one novel protein complex responsible for export of Vangl2 from the trans Golgi network.
  • Abnova mouse anti-mu1a was used to perform western blot in order to identify one novel protein complex responsible for export of Vangl2 from the trans Golgi network.
  • Abnova anti-TAF7 was used to perform western blot in order to study the functions of TAF7L in adipocyte differentiation.
  • Abnova PTP-SL protein was used to perform inhibition assay in order to show that cognitive deficits of Alzheimer's disease model could be reversed by STEP inhibitor.
  • Abnova HePTP protein was used to perform inhibition assay in order to show that cognitive deficits of Alzheimer's disease model could be reversed by STEP inhibitor.
  • Abnova mouse anti-coronin 1 was used to perform imunocytochemistry and western blotting assays in order to address the molecular mechanism underlying the coronin 1-dependent activation of cAMP/PKA signaling.
  • Abnova colorimetric assay was used to measure triglycerides in order to study the synaptic transmission and cognitive function impairment caused by reduction of the cholesterol sensor SCAP in the brains of mice.
  • Abnova HGF Mouse ELISA kit was used to perform ELISA in order to investigate the roles of Vav2 and Vav3 in skin cancer.
  • Abnova mouse anti-human LRRC39 polyclonal antibody was used to perform western blot and immunofluorescence microscopy in order to study a novel component of the sarcomeric M-band, LRRC39, and its role in stretch sensing.
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