Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Lipoprotein lipase Endocannabinoid related and lipase panel
Assay data:1 Tested
SummaryRelated BioAssays by Target
Inhibition of recombinant human LPL expressed in COS7 cells using PED-A1 containing DMPG vesicles as substrate pretreated for 20 mins followed by substrate addition and measured every 20 secs for 10 mins by fluorescence assay
Assay data:1 Active, 1 Activity ≤ 1 µM, 2 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of recombinant human LPL expressed in African green monkey COS7 cells using DGGR/DMPG vesicles as substrate pretreated for 10 mins followed by substrate addition and measured for 5 mins
Assay data:2 Tested
SummaryPubMed CitationRelated BioAssays by Target
Activation of bovine recombinant lipoprotein lipase at 100 uM using p-Nitrophenyl butyrate as substrate by HTS assay relative to NO-1886
Inhibition of bovine recombinant lipoprotein lipase at 100 uM using p-Nitrophenyl butyrate as substrate by HTS assay
Assay data:5 Active, 5 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Activation of bovine recombinant lipoprotein lipase at 100 uM using p-Nitrophenyl butyrate as substrate by HTS assay
Binding affinity to bovine recombinant lipoprotein lipase assessed as Km for substrate using p-Nitrophenyl butyrate as substrate by Lineweaver-Burk plot analysis (Rvb = 8.15 mM)
Induction of bovine LPL stabilization using intralipid as substrate at 25 uM preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate addition measured after 45 mins relative to control
Assay data:61 Tested
Induction of bovine LPL stabilization using intralipid as substrate at 12.5 uM preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate addition measured after 45 mins relative to control
Induction of bovine LPL stabilization using intralipid as substrate at 6.25 uM preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate addition measured after 45 mins relative to control
Induction of bovine LPL stabilization using intralipid as substrate at 3.12 uM preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate addition measured after 45 mins relative to control
Induction of bovine LPL stabilization using intralipid as substrate preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate addition measured after 45 mins relative to control
Assay data:3 Active, 3 Tested
Inhibition of lipoprotein lipase (unknown origin) at 100 uM incubated for 1 hr
Agonist activity at lipoprotein lipase (unknown origin) using p-nitrophenylbutyrate as substrate by spectrophotometric analysis relative to NO-1886
Activation of lipoprotein lipase (unknown origin) assessed as reversal of ANGPTL4-mediated enzyme inhibition treated with ANGPTL4 for 30 mins followed by substrate addition measured after 20 mins by spectrophotometric analysis
Assay data:3 Tested
Agonist activity at lipoprotein lipase (unknown origin) using p-nitrophenylbutyrate as substrate by spectrophotometric analysis relative to control
Assay data:6 Tested
Agonist activity at lipoprotein lipase (unknown origin) using p-nitrophenylbutyrate as substrate by spectrophotometric analysis
Agonist activity at lipoprotein lipase (unknown origin) using p-nitrophenylbutyrate as substrate at 40 uM by spectrophotometric analysis
Assay data:1 Active, 1 Tested
Inhibition of recombinant human lipoprotein lipase using bis-BODIPY-FL C11-PC as substrate preincubated for 30 mins followed by substrate addition by FELA method
Assay data:1 Active, 21 Tested
Inhibition of human LPL expressed in HEK293 cells using PED-A1 as substrate by spectrophotometry
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on