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Clin Chem ; 43(7): 1203-8, 1997 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-9216457

RESUMO

The analytical performance of the Tandem-R free PSA assay available from Hybritech Inc. was evaluated. Comparison of recoveries of purified free (unbound) prostate-specific antigen (PSA) diluted in female serum in the Tandem-R free PSA assay and the Tandem-R (total) PSA assay demonstrated a link in calibration between the assays and an accurate determination of percent free PSA. The cross-reactivity of the assay to purified PSA-alpha 1-antichymotrypsin was determined to be < 1%. The minimum-detectable concentration was < 0.05 microgram/L. The within-run and between-day CVs were < or = 5% for samples with > 0.3 microgram/L free PSA. Dilution and recovery showed no significant deviations from linearity across the assay range. The assay was insensitive to interference from blood components. The Tandem-R free PSA kit was shown to be an accurate, precise, and reliable assay for the measurement of free PSA.


Assuntos
Ensaio Imunorradiométrico/métodos , Antígeno Prostático Específico/sangue , Kit de Reagentes para Diagnóstico , Calibragem , Feminino , Humanos , Ensaio Imunorradiométrico/estatística & dados numéricos , Controle de Qualidade , Kit de Reagentes para Diagnóstico/estatística & dados numéricos , Sensibilidade e Especificidade , alfa 1-Antiquimotripsina/sangue
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