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stivali ugg Chemiluminescence immunoassay method o

 
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PostWysłany: Czw 7:47, 09 Gru 2010    Temat postu: stivali ugg Chemiluminescence immunoassay method o

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Chemiluminescence immunoassay method of calibration


After each test, there should be a certain cooling time, so that the tire pressure back to the cold tire pressure. Thus, to ensure continuous measurement repeatability conditions. 2 Taxi C values are measured (JJC517-1998 taxi meter \c large difference in value. and c, on the taxi meter \. order in the \. Even so, when measured, there are still problems. because the measurement procedures of the c values, knowledge was not sufficient. procedures section 4 of Appendix 1, the words \written ambiguous. to \values were quite different. what is reasonable, will do the analysis below. In addition, measurement c value, the tire's motion states, \more typical examples. a two car front seat, new tires, cold tire pressure to meet the requirements. ① tire main drum drive, turn on the device for 5 weeks to get a c active = 1.4%. ② main drum drive tire ,[link widoczny dla zalogowanych], turn on the device for 5 weeks to get c = a 0.3% passive. on the c value, the percentage of these two, described as \was different. The purpose of measuring the value of c is to minimize this difference. test when the device is the main drum drive tire \measurements shall be taken C passive. In other words, only the test, the tire main drum drive count, c take the initiative to have any meaning. But this does not match the requirements and procedures. In short, c value should be so measured. In the device, the main roller drive tire \suggested in Appendix 1, the value of the measurement conditions on the c,[link widoczny dla zalogowanych], to be clear limits, in order for the same tire, you can get the same c value is reasonable. Author: Zhou Qi. male, engineer. Work: Nanjing measurement tests. Communication After the address Cao Hongshan Village, Nanjing 210028 140. Received Time :2006-09-08 (on the next page 29) 4.4 Note in a calibration process to adopt the same type of immune control serum reference material; immune control serum dilution of the complex solution and its use should be in accordance with the requirements of the note; in the preparation of re-calibration solution can not be replaced by other liquids; with control serum remaining after the measurement should not keep doing the next day, the reagent material in some reactions The chemically unstable,[link widoczny dla zalogowanych], it will spread to the solution to, cause pollution leaving the results would be affected. 5 5.1 Technical requirements should be accompanied by the appearance of analyzer product brochures, product certificate and matching accessories; analyzer should not affect the performance of mechanical damage; the knobs, switches should be positioned accurately, with good function; sample stage should be smooth and clean; analyzer must be marked on the model, manufacture date, number and the make. 5.2 The accuracy of the standard biochemical reagents in the certificate required target value and better than 10%. 5.3 Repeatability standard biochemical reagents for the target value of the certificate request and ≤ 5%. 6 calibration process and calibration cycle calibrated chemiluminescence immunoassay analyzer calibration certificate or test issue report and indicate the calibration or test results. not exceeding one year calibration cycle. References [1] U.S. Congress, Clinical Laboratory Improvement Act Amendments (1998) (clinicallaboratoryimprovementamendment, CLIA'8Cool. [2] IS015189 \A quality and capacity requirements for>. [3] Ministry of Health,[link widoczny dla zalogowanych], \2000. About the author: He Bifen. Women engineers. Company: Shenzhen Academy of Metrology and Quality Inspection. Address: Shenzhen, Guangdong 518055, China. The King and Philosophy. Shenzhen Academy of Metrology and Quality Inspection (Shenzhen 518055). Received :2006 -08-29

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