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techniques [2023/10/29 17:24] – created quality_manager | techniques [2025/01/08 16:15] (current) – external edit 127.0.0.1 | ||
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2. Explain concept and application of Molar Absorptivity giving suitable examples. | 2. Explain concept and application of Molar Absorptivity giving suitable examples. | ||
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+ | 3. Draw diagram of a spectrophotometer. How double-beam-in-time spectrophotometer differ from double-beam-in-space spectrophotometer | ||
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+ | 4. Light sources in analytical equipments | ||
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+ | 5. Spectral isolation in optical analytical equipments | ||
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+ | 6. Wavelengh accuracy, spectral band width, stray light and photometric accuracy of optical analytical equipments | ||
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+ | 7. Principle, instrumentation and use of atomic absorption spectrometry in clinical chemistry | ||
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+ | 8. Zeeman correction in atomic absorption spectrometry | ||
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+ | 9. Principle of flurometry and fluroscence polarization | ||
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+ | 10. Components of flurometric equipment | ||
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+ | 11. Principles of Luminecence, | ||
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+ | 12. Principle and instrumentation of nephelometry and turbidimetry | ||
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+ | 13. Potentiometry using Ion selective electrodes for H+, Na+, K+ and Cl- | ||
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+ | 14. Potentiometry electrodes for pCO2 | ||
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+ | 15. Amperometric electrode for pO2 | ||
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+ | 16. Amperometric O2 based and H2O2 based glucose electrodes | ||
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+ | 17. Potentiometric enzyme electrode for blood urea | ||
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+ | 18. Biosensors – enzyme based and affinity based | ||
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+ | 19. Affinity sensors for specific protein and DNA detection | ||
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+ | 20. Electrophoresis support media | ||
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+ | 21. Isoelectric focusing | ||
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+ | 22. Principle of SDS PAGE | ||
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+ | 23. Troubleshooting SDS PAGE | ||
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+ | 24. Principle, | ||
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+ | 25. Microchip electrophoresis | ||
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+ | 26. Separation mechanisms used in chromatography | ||
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+ | 27. Size exclusion chromatography | ||
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+ | 28. Affinity chromatography | ||
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+ | 29. Explain chromatographic resolution and efficiency | ||
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+ | 30. Instrumentation of HPLC | ||
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+ | 31. HPLC sample injector | ||
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+ | 32. HPLC columns | ||
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+ | 33. HPLC detectors | ||
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+ | 34. Instrumentation of Gas Chromatography | ||
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+ | 35. GC detectors | ||
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+ | 36. Principle of electron and chemical ionization in mass spectrometer | ||
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+ | 37. Electrospray Ionization for mass spectrometry | ||
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+ | 38. MALDI mass spectrometry | ||
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+ | 39. Principles of various mass analysers for mass spectrometry | ||
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+ | 40. Quadruple mass analysers | ||
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+ | 41. Magnetic sector mass analysers | ||
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+ | 42. TOF mass analysers | ||
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+ | 43. Quadrupole and linear ion trap mass analysers | ||
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+ | 44. Tandom mass spectrometry | ||
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+ | 45. Clinical applications of mass spectrometer | ||
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+ | 46. Define isoenzymes. Explain genetic origin of isoenzymes. Enlist non-genetic modifications of enzymes | ||
+ | resulting in isoforms. | ||
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+ | 47. Measurement of enzymes by reaction rates | ||
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+ | 48. Strategy for detection of above-linearity range ALT in automated chemistry analysers | ||
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+ | 49. Traceability of enzyme measurement | ||
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+ | 50. Enzymes as analytical reagents | ||
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+ | 51. Monoclonal antibody productions | ||
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+ | 52. Labeled immunochemical assays | ||
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+ | 53. Competitive vs. noncompetitive immunoassay | ||
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+ | 54. Labels used for nonisotopic immunoassay and their detection limits | ||
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+ | 55. Heterogenous vs. homogenous immunoassay | ||
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+ | 56. CEDIA and EMIT | ||
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+ | 57. Homogenous polarization fluroimmunoassay | ||
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+ | 58. Principle of PCR | ||
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+ | 59. PCR optimization and primer design | ||
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+ | 60. PCR contamination control | ||
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+ | 61. Hot start PCR | ||
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+ | 62. Asymmetric PCR | ||
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+ | 63. Allele specific PCR | ||
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+ | 64. Single molecule PCR | ||
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+ | 65. Isothermic PCR amplification based on transcription | ||
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+ | 66. PCR application detection techniques | ||
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+ | 67. PCR amplicon discrimination techniques | ||
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+ | 68. PCR-RFLP | ||
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+ | 69. Single stranded conformation polymorphism for discrimination of PCR products | ||
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+ | 70. Denaturing gradient and temperature gradient electrophoresis for discrimination of PCR products | ||
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+ | 71. Dideoxy terminal sequencing of DNA principle and automated sequencing | ||
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+ | 72. Emulsion PCR | ||
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+ | 73. Bridge amplification | ||
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+ | 74. Absorbance melting curve of double helical nucleic acid | ||
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+ | 75. Dot-blot hybridization assay | ||
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+ | 76. Two color DNA microarray | ||
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+ | 77. DNA copy number variation assay | ||
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+ | 78. Single copy visualization assay | ||
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+ | 79. real time PCR with dsDNA binding dyes | ||
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+ | 80. Real time monitoring of PCR and melting analysis | ||
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+ | 81. Detection, | ||
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+ | 82. Common probes and dyes for realtime PCR | ||
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+ | 83. Microchip electrophoresis device | ||
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+ | 84. Automation in sample identification and data collection | ||
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+ | 85. Automation in sample transporters | ||
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+ | 86. Describe components of a automated discrete analyser. | ||
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+ | 87. Use of barcoding in clinical laboratory | ||
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+ | 88. Components of Integrated automation system in clinical laboratory | ||
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+ | 89. Advantages and disadvantages of POCT | ||
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+ | 90. Ideal requirements of POCT | ||
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+ | 91. Classification of POCT devices | ||
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+ | 92. Principle of electrochemical glucose strip used in glucometers | ||
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+ | 93. Principle of lateral flow immunoassay | ||
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+ | 94. Principles of HbA1C POCT instruments | ||
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+ | 95. Assessing need for POCT servic | ||
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