hdl-cholesterol direct

Aplicaciones en ADVIA 1650Applications on ADVIA 1650HDL-CHOLESTEROL DIRECTHDL-Cholesterol Direct (40 mL), Code 11 335 05HDL-Cholesterol Direct (320 mL), Code 11 335 10HDL-Cholesterol Direct (1000 mL), Code 11 335 15USOUSEMETODOMETHODMUESTRASAMPLEREACTIVOSREAGENTSESTABILIDADSTABILITYCALIBRADORSTANDARDCONTROL CALIDADQUALITY CONTROLDETERMINACIONESNUMBER OF TESTSLINEALIDADLINEARITYINTERFERENCIASINTERFERENCESNOTANOTENOTA DE AVISOWARNINGReactivo de diagnóstico in vitro para la determinación de laslipoproteínas de alta densidad (HDL) en suero o plasma.In vitro diagnostic reagent for the determination of high densitylipoproteins (HDL) in serum or plasma.Enzimático colorimétricoEnzymatic colorimetricSuero o plasma heparinizado u obtenido con EDTASerum or EDTA or heparinized plasmaReactivo de trabajo: Los reactivos R1 y R2 están listos para suuso.Working reagent: The reagents R1 and R2 are ready to use.Reactivo de trabajo: Hasta fecha de caducidad, cerradosinmediatamente después de su uso y conservados a 2-8ºC.Working reagent: Stable until expiry date, closed after use andstored at 2-8ºC.HDL/LDL Calibrator, Code 19 720 05Linear Human Multisera Normal, Code 19 800 05Linear Human Multisera Abnormal, Code 19 850 05400 tests/kit, Code 11 335 053200 tests/kit, Code 11 335 1010000 tests/kit, Code 11 335 15(no se considera el volumen muerto)(dead volume is not taken in consideration)Hasta 150 mg/dL (3,89 mmol/L).Up to 150 mg/dL (3.89 mmol/L).Bilirrubina, hemoglobina y lípidos no interfieren.Bilirubin, hemoglobin and lipids do not interfere.Para más información lea el prospecto del reactivo.For additional information read reagent packaging insert.La aplicación incluida se da solamente como pauta. Cualquieraplicación deberá ser validada con el fin de demostrar que secumplen las características analíticas del método.The reported application is given only as a guideline. Any applicationto an instrument should be validated to demonstrate that resultsmeet the performance characteristics of the method.

HDL-Cholesterol DirectADVIA 1650ANALYTICAL PARAMETERS Reanalysis conditions Multi-Standards settingAnalytical Conditions Serum reac. Smp. vol. (µ) 3.00 Formula Linear correction Axis conv. No convert.R1 volume 75.00 Serum dilut. Method (µ) None Points 2R2 volume 0.00 Serum reac. Smp. vol. (d) 3.00R3 volume 25.00 Serum dilut.method (d) None FV MEANR4 volume 0.00 BLK 0.00 ...R1 diluent vol. 0.00 Standards setting 1 * ...R2 diluent vol. 0.00 BLK H 0.0500R3 diluent vol. 0.00 BLK L -0.0100R4 diluent vol. 0.00 STD H 0.1000 * assigned valueSerum reac.s. vol. 5.0 STD L 0.0030Serum dil. method Standard FV *Serum dil. S. vol 30.0 Abnml. (serum) H 99999Serum dil. Volume 120.0 Abnml. (serum) L -9999Serum dil. posit 0Reaction timeReagent 1 stir.Reagent 2 stir.10 min.WeakWeakReagent 3 stir. Weak Calculation method setting Reaction rate methodReagent 4 stir. Weak M-DET. P.I. 0 Prozone Cycle 3M-DET. P.m. 83 Prozone form. None Factor 3.0Sub-analy. Conditions M-DET. P.n. 84 Prozone limit 9.999 Reac. Type Inc.Name HDL-c S-DET. P.p. 53 Prozone judge Upper limit E2 corre. Not doDigits 0 S-DET. P.r. 54 Judge limit 9.999 Blank (µ) 9.9999M-wave. L. 596 nm M-DET. P.m. 0 Blank (d) -9.999S-wave. L. 694nm Check D.P.I. 0 M-DET. P.n. 0 Sample (µ) 9.9999Analy. mthd. EPA Limit value 0.003 S-DET. P.p. 0 Sample (d) -9.999Calc. mthd. STD Variance 10.0 S-DET. P.r. 0Qualit. judg. Not do Endpoint methodRe. Absorb (µ) 0.5000Re. Absorb (d) 0.000011335ADVIA 1650-1/0407