Inhibition of Mycobacterium tuberculosis H37Ra PTPB expressed in Escherichia coli BL21 (DE3) using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured for 5 mins by spectrophotometric analysis
Inhibition of Mycobacterium tuberculosis H37Ra PTPB expressed in Escherichia coli BL21 (DE3) at 50 uM using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured for 5 mins by spectrophotometric analysis
Inhibition of Mycobacterium PTPB at 50 uM using p-nitrophenyl phosphate as substrate incubated for 10 mins followed by substrate addition and measured for 5 mins by spectrophotometric method
Inhibition of Mycobacterium tuberculosis H37Rv His-tagged ptpB expressed in Escherichia coli BL21(DE3) using pNPP as substrate preincubated for 15 mins followed by substrate addition and measured after 15 mins
Inhibition of Mycobacterium tuberculosis H37Rv ATCC 35837 ptpB infected in human THP1 cells assessed as reduction in intracellular bacterial burden at 20 to 100 uM after 72 hrs post infection relative to DMSO-treated control
Inhibition of multi-drug resistant Mycobacterium tuberculosis Beijing-W_565 ptpB infected in human THP1 cells assessed as reduction in intracellular bacterial burden at 20 to 100 uM after 72 hrs post infection relative to DMSO-treated control
Inhibition of Mycobacterium tuberculosis H37Rv ATCC 35837 ptpB infected in human THP1 cells assessed as reduction in intracellular bacterial burden at 10 to 80 uM after 72 hrs post infection relative to DMSO-treated control
Inhibition of multi-drug resistant Mycobacterium tuberculosis Beijing-W_565 ptpB infected in human THP1 cells assessed as reduction in intracellular bacterial burden at 20 to 80 uM after 72 hrs post infection relative to DMSO-treated control
Inhibition of RFP expressing Mycobacterium tuberculosis H37Rv ATCC 35837 ptpB infected in mouse RAW264.7 cells assessed as prolongation association of PI3P to FYVE2X-FGFP on bacterial phagosome at 80 uM by live-cell imaging method
Inhibition of Mycobacterium tuberculosis PtpB using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured every minute for 10 mins by UV-VIS spectrophotometric analysis
Competitive inhibition of Mycobacterium tuberculosis PtpB using p-nitrophenyl phosphate as substrate up to 0.3 uM preincubated for 10 mins followed by substrate addition measured every minute for 10 mins by Michaelis-Menten plot analysis
Non-competitive inhibition of Mycobacterium tuberculosis PtpB using p-nitrophenyl phosphate as substrate up to 0.3 uM preincubated for 10 mins followed by substrate addition measured every minute for 10 mins by Michaelis-Menten plot analysis
Inhibition of Mycobacterium tuberculosis PtpB using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured every minute for 10 mins by Michaelis-Menten plot analysis
Reversible inhibition of Mycobacterium tuberculosis PtpB using p-nitrophenyl phosphate as substrate assessed as enzyme recovery at 10 times IC50 preincubated for 10 mins followed by 100-fold dilution
Time independent inhibition of Mycobacterium tuberculosis PtpB at 0.2 uM pre-incubated for 0 to 10 mins before p-nitrophenyl phosphate substrate addition