characterized by their frequency and wavelength 2. It is the distance between two successive peaks 3. It is the unit used in expressing wavelength 4. The formula that describes the relationship between the wavelength and energy 5. The formula used in the answer in question number 4 6. It is the number of vibrations of wave motion per second 7. Relation of the wavelength to frequency and energy 8. The ____ the wavelength , the higher the frequency/energy 9. It represents the wavelength In nanometers at peak transmittance 10. It is the wavelength indicated on the control dial 11. Actual wavelength of light passed on the monochromator 12. Used to check wavelength accuracy (wavelength calibration) 13. Verify absorbance accuracy on linearity 14. Is the isolation of discreet portions of the spectrum for purposes of measurement 15. Measurement of light intensity in a narrower wavelength 16. Measurement of light intensity 17. Involves measurement of the light transmitted by a solution to determine the concentration of the light absorbing substances in the solution 18. It is the simplest type of absorption spectrophotometer 19. It splits the monochromatic light into two components- one beam passes through the sample and the other through a reference solution or blank 20. It is designed to make one measurement at one specified wavelength 21. What must be known in advance when a single beam instrument is used 22. It corrects the variation in light source intensity 23. The absorbance of the sample can be directly recorded as the electrical output of the sample beam 24. Type of double beam spectrophotometer that uses 2 photodetectors, for the sample beam and reference beam 25. It uses one photodetectors and alternately passes the monochromatic light through the sample cuvet and then reference cuvet using a chopper or rotating sector mirror 26. It provides polychromatic light and must generate sufficient radiant energy or power to measure the analyte of interest 27. What is directed through the monochromator and the sample? 28. The response to change in light must be ___ to give accurate absorbance measurements throughout its absorbance angles 29. It emits radiation that changes in intensity, it is widely used in the laboratory 30. It is the commonly used light source in the visible and near infrared region 31. It is routinely used to provide UV radiation in analytic spectrometers 32. It produces a continuous source of radiation which covers both the UV and the visible range 33. It emits limited radiation and wavelength it finds wide use in atomic absorption molecular and fluorescent spectroscopy 34. It is also used as a light sources for spectrophotometry 35. It minimizes unwanted or stray light and prevents the entrance of scattered light into the monochromator system 36. Refers to any wavelength outside the bad transmitted by the monochromator; does not originate from the polychromatic light source 37. It causes absorbance error 38. It is the most common cause of loss of linearity at high analyte concentration and it limits the maximum absorbance that a spectrophotometer can achieve 39. It isolates specific or individual wavelength of light 40. Are wedge-shaped pieces of glass, glass or sodium chloride 41. It is most commonly used and has a better resolution than a prism 42. Are simple monochromators that are least expensive and not precise but useful 43. It is made by cutting grooves or slits into an aluminized surface of a flat piece of crown glass 44. It produce monochromatic light based on the principle of constructive interference of waves 45. Kind of monochromator that can be rotated, allowing only the desired wavelength to pass through an exit slit. 46. What is refracted on a prism as it enter the more dense glass 47. It controls the width of light beam 48. It is the total range of wavelengths transmitted 49. It requires a bandpass less than 1/5 the natural bandpass of the spectrophotometer 50. A function of the type of device used and the width of entrance and exit slits 51. It is reflected by the bandpass that is the narrower the bandpass the greater the resolution. 52. Is called absorption cell/ analytical cell/ sample cell 53. Holds the solution whose concentration is to be measured. 54. It is a kind of cuvet that is most commonly used and can be used in 350-2000 nm 55. Used for measurement of solution requiring visible and ultraviolet spectra 56. It scatters light and should be discarded 57. Transmit light effectively at wavelengths >220nm 58. Path lengths of cuvet 59. Length given to cuvettes to increase sensitivity 60. It detects and converts transmitted light into photoelectric energy and detects the amount of light that passes through the sample in a cuvette 61. It is the simplest least expensive and a temperature sensitive kind of detector 62. What kind of detector is used in filter photometers with a wide bandpass and used for detecting and measuring radiation in the visible region 63. It contains cathode and anode enclosed in a glass case 64. It is the most commonly used detector that measures visible and UV regions 65. It requires an external voltage for operation and has a photosensitive material that gives off electron when light energy strikes it 66. It has an excellent sensitivity and has a rapid response and should never be exposed to room light 67. It is not as sensitive as PMT but with excellent linearity and measures light at a multitude of wavelengths 68. Most useful as a simultaneous multichannel detector 69. It displays output of the detection system 70. It states that the concentration of the unknown substance is directly proportional to the absorbed light and inversely proportional to the amount of transmitted light 71. It is the amount of light absorbed 72. Ratio of the radiant energy transmitted divided by the radiant energy incident on the sample 73. Formula to get the percent transmittance 74. This means that the blank contains serum but without the reagent to compete the assay 75. It corrects absorbance caused by the color of the reagents 76. Measures the absorbance of the sample and reagent in the absence of the end product 77. Used to correct for artifactal absorbance readings 78. Measures the light emitted by a single atom burned in flame 79. Light source of FEP 80. Indicates changes in the fuel reading of the instrument 81. Corrects variations in flame and atomizer characteristics 82. It measures the light absorbed atoms disassociated by heat 83. Used for measurement of excited ions 84. Light source of AAS 85. Used to convert ions to atoms 86. Used to modulate the light source 87. Meaning of EDTA 88. Used in chloride test 89. Used in calcium test 90. The unknown sample is made to react with known solution in presence of an indicator 91. It is used for measuring abundant large particles proteins and bacterial suspensions 92. Used to detect bacterial growth in broth cultures 93. Used to detect clot formation 94. Used for measuring amount of antigen antibody complexes 95. It is the migration of charged particles in an electric field 96. It separates proteins based on their electric charge densities 97. Determine the net charge on a protein, hence its electrophoretic mobility 98. Has a net charge that can be either positive or negative depending on pH conditions 99. Is the movement of buffer ions and solvent relative to the fixed support 100. Migration of small charged ions 101. Migration of charged macromolecules 102. Separates by molecular size 103. Separats by electrical charge and does not bind protein 104. Separates on the basis of charge and molecular size; separates proteins into 20 fractions and is used to study isoenzymes 105. Movement of buffer and solvent relative to their fixed support 106. Separating molecules migrate through a pH gradient 107. Separation is formed in narrow bore fuse silica capillaries 108. Measures the absorbance of stain concentration of dye and protein fraction 109. It scans and quantitates electrophoretic pattern 110. Separates molecules by migration through a pH gradient 111. Is ideal for separating proteins of identical sizes but with different net charges 112. In this method sample molecules are separated by electro-osmotic flow 113. Synthesize DNA