Differences
This shows you the differences between two versions of the page.
Both sides previous revision Previous revision Next revision | Previous revision | ||
techniques [2023/10/29 17:31] – quality_manager | techniques [2025/01/08 16:15] (current) – external edit 127.0.0.1 | ||
---|---|---|---|
Line 5: | Line 5: | ||
3. Draw diagram of a spectrophotometer. How double-beam-in-time spectrophotometer differ from double-beam-in-space spectrophotometer | 3. Draw diagram of a spectrophotometer. How double-beam-in-time spectrophotometer differ from double-beam-in-space spectrophotometer | ||
- | 4. Light sources in analytical equipments | + | 4. Light sources in analytical equipments |
- | 5. Spectral isolation in optical analytical equipments | + | 5. Spectral isolation in optical analytical equipments |
- | 6. Wavelengh accuracy, spectral band width, stray light and photometric accuracy of optical analytical equipments | + | 6. Wavelengh accuracy, spectral band width, stray light and photometric accuracy of optical analytical equipments |
- | 7. Principle, | + | 7. Principle, instrumentation and use of atomic absorption spectrometry in clinical chemistry |
- | 8. Zeeman correction in atomic absorption spectrometry | + | 8. Zeeman correction in atomic absorption spectrometry |
- | 9. Principle of flurometry and fluroscence polarization | + | 9. Principle of flurometry and fluroscence polarization |
- | 10. Components of flurometric equipment | + | 10. Components of flurometric equipment |
- | 11. Principles of Luminecence, | + | 11. Principles of Luminecence, |
- | 12. Principle and instrumentation of nephelometry and turbidimetry | + | 12. Principle and instrumentation of nephelometry and turbidimetry |
- | 13. Potentiometry using Ion selective electrodes for H+, Na+, K+ and Cl- | + | 13. Potentiometry using Ion selective electrodes for H+, Na+, K+ and Cl- |
- | 14. Potentiometry electrodes for pCO2 | + | 14. Potentiometry electrodes for pCO2 |
- | 15. Amperometric electrode for pO2 | + | 15. Amperometric electrode for pO2 |
- | 16. Amperometric O2 based and H2O2 based glucose electrodes | + | 16. Amperometric O2 based and H2O2 based glucose electrodes |
+ | |||
+ | 17. Potentiometric enzyme electrode for blood urea | ||
+ | |||
+ | 18. Biosensors – enzyme based and affinity based | ||
+ | |||
+ | 19. Affinity sensors for specific protein and DNA detection | ||
+ | |||
+ | 20. Electrophoresis support media | ||
+ | |||
+ | 21. Isoelectric focusing | ||
+ | |||
+ | 22. Principle of SDS PAGE | ||
- | 17. Potentiometric enzyme electrode for blood urea | ||
- | 18. Biosensors – enzyme based and affinity based | ||
- | 19. Affinity sensors for specific protein and DNA detection | ||
- | 20. Electrophoresis support media | ||
- | 21. Isoelectric focusing | ||
- | 22. Principle of SDS PAGE | ||
23. Troubleshooting SDS PAGE | 23. Troubleshooting SDS PAGE | ||
+ | |||
24. Principle, | 24. Principle, | ||
+ | |||
25. Microchip electrophoresis | 25. Microchip electrophoresis | ||
+ | |||
26. Separation mechanisms used in chromatography | 26. Separation mechanisms used in chromatography | ||
+ | |||
27. Size exclusion chromatography | 27. Size exclusion chromatography | ||
+ | |||
28. Affinity chromatography | 28. Affinity chromatography | ||
+ | |||
29. Explain chromatographic resolution and efficiency | 29. Explain chromatographic resolution and efficiency | ||
+ | |||
30. Instrumentation of HPLC | 30. Instrumentation of HPLC | ||
+ | |||
31. HPLC sample injector | 31. HPLC sample injector | ||
+ | |||
32. HPLC columns | 32. HPLC columns | ||
+ | |||
33. HPLC detectors | 33. HPLC detectors | ||
+ | |||
34. Instrumentation of Gas Chromatography | 34. Instrumentation of Gas Chromatography | ||
+ | |||
35. GC detectors | 35. GC detectors | ||
+ | |||
36. Principle of electron and chemical ionization in mass spectrometer | 36. Principle of electron and chemical ionization in mass spectrometer | ||
+ | |||
37. Electrospray Ionization for mass spectrometry | 37. Electrospray Ionization for mass spectrometry | ||
+ | |||
38. MALDI mass spectrometry | 38. MALDI mass spectrometry | ||
+ | |||
39. Principles of various mass analysers for mass spectrometry | 39. Principles of various mass analysers for mass spectrometry | ||
+ | |||
40. Quadruple mass analysers | 40. Quadruple mass analysers | ||
+ | |||
41. Magnetic sector mass analysers | 41. Magnetic sector mass analysers | ||
+ | |||
42. TOF mass analysers | 42. TOF mass analysers | ||
+ | |||
43. Quadrupole and linear ion trap mass analysers | 43. Quadrupole and linear ion trap mass analysers | ||
+ | |||
44. Tandom mass spectrometry | 44. Tandom mass spectrometry | ||
+ | |||
45. Clinical applications of mass spectrometer | 45. Clinical applications of mass spectrometer | ||
- | 46. Define isoenzymes. Explain genetic origin of isoenzymes. Enlist non-genetic modifications of enzymes resulting in isoforms. | + | |
+ | 46. Define isoenzymes. Explain genetic origin of isoenzymes. Enlist non-genetic modifications of enzymes | ||
+ | resulting in isoforms. | ||
47. Measurement of enzymes by reaction rates | 47. Measurement of enzymes by reaction rates | ||
+ | |||
48. Strategy for detection of above-linearity range ALT in automated chemistry analysers | 48. Strategy for detection of above-linearity range ALT in automated chemistry analysers | ||
+ | |||
49. Traceability of enzyme measurement | 49. Traceability of enzyme measurement | ||
+ | |||
50. Enzymes as analytical reagents | 50. Enzymes as analytical reagents | ||
+ | |||
51. Monoclonal antibody productions | 51. Monoclonal antibody productions | ||
+ | |||
52. Labeled immunochemical assays | 52. Labeled immunochemical assays | ||
+ | |||
53. Competitive vs. noncompetitive immunoassay | 53. Competitive vs. noncompetitive immunoassay | ||
+ | |||
54. Labels used for nonisotopic immunoassay and their detection limits | 54. Labels used for nonisotopic immunoassay and their detection limits | ||
+ | |||
55. Heterogenous vs. homogenous immunoassay | 55. Heterogenous vs. homogenous immunoassay | ||
+ | |||
56. CEDIA and EMIT | 56. CEDIA and EMIT | ||
+ | |||
57. Homogenous polarization fluroimmunoassay | 57. Homogenous polarization fluroimmunoassay | ||
+ | |||
58. Principle of PCR | 58. Principle of PCR | ||
+ | |||
59. PCR optimization and primer design | 59. PCR optimization and primer design | ||
+ | |||
60. PCR contamination control | 60. PCR contamination control | ||
+ | |||
61. Hot start PCR | 61. Hot start PCR | ||
+ | |||
62. Asymmetric PCR | 62. Asymmetric PCR | ||
+ | |||
63. Allele specific PCR | 63. Allele specific PCR | ||
+ | |||
64. Single molecule PCR | 64. Single molecule PCR | ||
+ | |||
65. Isothermic PCR amplification based on transcription | 65. Isothermic PCR amplification based on transcription | ||
+ | |||
66. PCR application detection techniques | 66. PCR application detection techniques | ||
+ | |||
67. PCR amplicon discrimination techniques | 67. PCR amplicon discrimination techniques | ||
+ | |||
68. PCR-RFLP | 68. PCR-RFLP | ||
+ | |||
69. Single stranded conformation polymorphism for discrimination of PCR products | 69. Single stranded conformation polymorphism for discrimination of PCR products | ||
+ | |||
70. Denaturing gradient and temperature gradient electrophoresis for discrimination of PCR products | 70. Denaturing gradient and temperature gradient electrophoresis for discrimination of PCR products | ||
+ | |||
71. Dideoxy terminal sequencing of DNA principle and automated sequencing | 71. Dideoxy terminal sequencing of DNA principle and automated sequencing | ||
+ | |||
72. Emulsion PCR | 72. Emulsion PCR | ||
+ | |||
73. Bridge amplification | 73. Bridge amplification | ||
+ | |||
74. Absorbance melting curve of double helical nucleic acid | 74. Absorbance melting curve of double helical nucleic acid | ||
+ | |||
75. Dot-blot hybridization assay | 75. Dot-blot hybridization assay | ||
+ | |||
76. Two color DNA microarray | 76. Two color DNA microarray | ||
+ | |||
77. DNA copy number variation assay | 77. DNA copy number variation assay | ||
+ | |||
78. Single copy visualization assay | 78. Single copy visualization assay | ||
+ | |||
79. real time PCR with dsDNA binding dyes | 79. real time PCR with dsDNA binding dyes | ||
+ | |||
80. Real time monitoring of PCR and melting analysis | 80. Real time monitoring of PCR and melting analysis | ||
+ | |||
81. Detection, | 81. Detection, | ||
+ | |||
82. Common probes and dyes for realtime PCR | 82. Common probes and dyes for realtime PCR | ||
+ | |||
83. Microchip electrophoresis device | 83. Microchip electrophoresis device | ||
+ | |||
84. Automation in sample identification and data collection | 84. Automation in sample identification and data collection | ||
+ | |||
85. Automation in sample transporters | 85. Automation in sample transporters | ||
+ | |||
86. Describe components of a automated discrete analyser. | 86. Describe components of a automated discrete analyser. | ||
+ | |||
87. Use of barcoding in clinical laboratory | 87. Use of barcoding in clinical laboratory | ||
+ | |||
88. Components of Integrated automation system in clinical laboratory | 88. Components of Integrated automation system in clinical laboratory | ||
+ | |||
89. Advantages and disadvantages of POCT | 89. Advantages and disadvantages of POCT | ||
+ | |||
90. Ideal requirements of POCT | 90. Ideal requirements of POCT | ||
+ | |||
91. Classification of POCT devices | 91. Classification of POCT devices | ||
+ | |||
92. Principle of electrochemical glucose strip used in glucometers | 92. Principle of electrochemical glucose strip used in glucometers | ||
+ | |||
93. Principle of lateral flow immunoassay | 93. Principle of lateral flow immunoassay | ||
+ | |||
94. Principles of HbA1C POCT instruments | 94. Principles of HbA1C POCT instruments | ||
+ | |||
95. Assessing need for POCT servic | 95. Assessing need for POCT servic | ||
+ |