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  • Anti-MBP antibody was used for in vitro binding assay, in order to study the role of Bub1 in the process of spindle assembly checkpoint.
  • Amilose resin was used for in vitro binding assay, in order to study the role of Bub1 in the process of spindle assembly checkpoint.
  • 3'-O-Me-m7GpppG was used in this study to perform ribosome profiling on cultured human cells under conditions of severe stress induced with sodium arsenite.
  • lambda-protein phosphatase was used for kinase assay, in order to study the mechanism by which MAPKAPK2/MAPKAPK3 activate starvation-induced autophagy.
  • New England Biolabs Q5 DNA polymerase was used to perform DNA mutation in order to study the mechanism by which the bipartite centrosome regulates the apicomplexan cell cycle.
  • NEB Phusion DNA Polymerase was used to perform DNA amplification in order to study the role of Ldb2a in the homeostatic control of TGFbeta signalling.
  • NEB high fidelity Phusion hot start polymerase was used to perform DNA amplification in order to study the role of transcription factor ZEB1 in the adipogenic gene regulatory network.
  • NEB NEBNext Multiplex Oligos were used to perform DNA library preparation in order to study the assembly of Rev-RRE nuclear export complexes.
  • New England Biolabs T7 Express Crystal cells were used to perform protein expression in order to study the regulation mechanism of periplasmic proteolysis by the signaling molecule cyclic-di-GMP.
  • New England Biolabs E. coli BL21 T7 Express cells were used to perform protein expression in order to study the regulation mechanism of periplasmic proteolysis by the signaling molecule cyclic-di-GMP.
  • NEB MNase was used to perform chromatin fragmentation in order to study the regulation of nuclear receptor HNF4A by TAF4 during post-natal hepatocyte differentiation.
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