PMC:7795856 / 32819-34206 JSONTXT

{"project":"LitCovid-PubTator","denotations":[{"id":"580","span":{"begin":204,"end":217},"obj":"Gene"},{"id":"581","span":{"begin":569,"end":572},"obj":"Gene"},{"id":"582","span":{"begin":720,"end":723},"obj":"Gene"},{"id":"583","span":{"begin":845,"end":865},"obj":"Gene"},{"id":"584","span":{"begin":891,"end":911},"obj":"Gene"},{"id":"585","span":{"begin":1288,"end":1291},"obj":"Gene"},{"id":"586","span":{"begin":300,"end":303},"obj":"Species"},{"id":"587","span":{"begin":459,"end":462},"obj":"Species"},{"id":"588","span":{"begin":595,"end":598},"obj":"Species"},{"id":"589","span":{"begin":1314,"end":1317},"obj":"Species"},{"id":"590","span":{"begin":1060,"end":1083},"obj":"Chemical"},{"id":"591","span":{"begin":779,"end":785},"obj":"Disease"}],"attributes":[{"id":"A580","pred":"tao:has_database_id","subj":"580","obj":"Gene:213"},{"id":"A581","pred":"tao:has_database_id","subj":"581","obj":"Gene:50719"},{"id":"A582","pred":"tao:has_database_id","subj":"582","obj":"Gene:50719"},{"id":"A583","pred":"tao:has_database_id","subj":"583","obj":"Gene:16870"},{"id":"A584","pred":"tao:has_database_id","subj":"584","obj":"Gene:16870"},{"id":"A585","pred":"tao:has_database_id","subj":"585","obj":"Gene:50719"},{"id":"A586","pred":"tao:has_database_id","subj":"586","obj":"Tax:10116"},{"id":"A587","pred":"tao:has_database_id","subj":"587","obj":"Tax:10116"},{"id":"A588","pred":"tao:has_database_id","subj":"588","obj":"Tax:10116"},{"id":"A589","pred":"tao:has_database_id","subj":"589","obj":"Tax:10116"},{"id":"A590","pred":"tao:has_database_id","subj":"590","obj":"MESH:C008644"},{"id":"A591","pred":"tao:has_database_id","subj":"591","obj":"MESH:D011535"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"A 96-well Nunc Maxisorb ELISA plate (ThermoFisher) was coated with 100 µg/mL anti-PAS antibody in PBS at 4 °C overnight. After washing twice with PBS/T, free binding sites were blocked with 3% w/v bovine serum albumin (BSA) in PBS/T at room temperature for 1 h. After washing 3 times with PBS/T, the rat plasma samples were applied in dilution series in PBS/T supplemented with 0.5% (v/v) plasma from an untreated animal (to maintain a constant proportion of rat plasma constituents). In the same manner, a standard curve was prepared using dilution series of purified Tα1-PAS (used for spiking rat plasma) at defined concentrations. After incubation for 1 h at RT, wells were washed 3 times with PBS/T. To detect bound Tα1-PAS, wells were incubated for 1 h with 50 µl of a 1 µg/mL PBS/T solution of the second anti-PAS antibody conjugated with alkaline phosphatase using the Lightning-Link alkaline phosphatase antibody labeling kit (BioTechne, Wiesbaden, Germany). After washing twice with PBS/T and twice with PBS, the enzymatic activity was detected using p-nitrophenyl phosphate (0.5 mg/mL). To this end, the plate was incubated for 20 min at 30 °C, the absorbance was measured at 405 nm using a SpectraMax M5e microtiter plate reader (Molecular Devices, Sunnyvale, CA, USA) and the Tα1-PAS concentrations in rat plasma samples were quantified by comparison with the standard curve."}

{"project":"LitCovid-sentences","denotations":[{"id":"T201","span":{"begin":0,"end":120},"obj":"Sentence"},{"id":"T202","span":{"begin":121,"end":261},"obj":"Sentence"},{"id":"T203","span":{"begin":262,"end":484},"obj":"Sentence"},{"id":"T204","span":{"begin":485,"end":633},"obj":"Sentence"},{"id":"T205","span":{"begin":634,"end":703},"obj":"Sentence"},{"id":"T206","span":{"begin":704,"end":966},"obj":"Sentence"},{"id":"T207","span":{"begin":967,"end":1096},"obj":"Sentence"},{"id":"T208","span":{"begin":1097,"end":1387},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A 96-well Nunc Maxisorb ELISA plate (ThermoFisher) was coated with 100 µg/mL anti-PAS antibody in PBS at 4 °C overnight. After washing twice with PBS/T, free binding sites were blocked with 3% w/v bovine serum albumin (BSA) in PBS/T at room temperature for 1 h. After washing 3 times with PBS/T, the rat plasma samples were applied in dilution series in PBS/T supplemented with 0.5% (v/v) plasma from an untreated animal (to maintain a constant proportion of rat plasma constituents). In the same manner, a standard curve was prepared using dilution series of purified Tα1-PAS (used for spiking rat plasma) at defined concentrations. After incubation for 1 h at RT, wells were washed 3 times with PBS/T. To detect bound Tα1-PAS, wells were incubated for 1 h with 50 µl of a 1 µg/mL PBS/T solution of the second anti-PAS antibody conjugated with alkaline phosphatase using the Lightning-Link alkaline phosphatase antibody labeling kit (BioTechne, Wiesbaden, Germany). After washing twice with PBS/T and twice with PBS, the enzymatic activity was detected using p-nitrophenyl phosphate (0.5 mg/mL). To this end, the plate was incubated for 20 min at 30 °C, the absorbance was measured at 405 nm using a SpectraMax M5e microtiter plate reader (Molecular Devices, Sunnyvale, CA, USA) and the Tα1-PAS concentrations in rat plasma samples were quantified by comparison with the standard curve."}