Instruments and measurements Flashcards

1
Q

Absorbance equation?

How do we get around the fact plasma/serum have lots of things in it?

Where two compounds have same absorbence called?

A

A= a (constant) x b (path of light) x c (concentration)

React what we want to specific compound and use Beer-Lambert law (use a Blank) or Allen correction (measure Aborbance equodistant)

Isobestic point

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2
Q

What is a half band pass?

Detectors on light instruments tend to be?

A

Measure of width of peak at half height; measures how precise light is

Diode arrays; can measure various waves of light

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3
Q

What is nephelometry?

Usage?

What is turbidity?

What interfears with both?

A

Measure dispersion from particles; measure at an ANGLE; more precise but need whole machine

Antigen-antibodies;

Turbidity: measured decrease in light (A) by particles. use photometer

lipemia interfears

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4
Q

What is atomic absorption?

A

Element absorb light emitted by same element in cathode tube

Measure decreased intensity when passing through vaporized element

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5
Q

What is standard vs reverse chromotography?

How to improve resolution?

A

Standard: Mobile phase non-polar, stantionary polar
Reverse is mobile polar and stationary non-polar

Increase length, decrease particle size, altering mobile phase–best way to pick up speed

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6
Q

If seperating Anions (-) use what column?

Ion exchange in labs used for?

A

Positive. If (+) ions seperated use (-) column

HbA1c which binds to boronate

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7
Q

What test can be used to look for volitiles?

In electrophoresis what is isoelectric point?

Electrophorisis above pI makes protein’s negative so they go to?

A

Head space gas chromatogaphy!

pH is neutral: if pH > negative, if pH < net positive

Positive end of the strip; the anode; ANIONS GO TO ANODE

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8
Q

What is electroendosmosis?

A

Some small proteins like immunoglobulins go towards cathode (the - charged electrode)

Some electrophoretic media is charged and moves dragging the small molecules with it

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9
Q

How to quantify proteins in a gel?

A

Densitometer after staining

Proteins: Coomassie blue, Pnceau red-s

DNA: ethidium bromide

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10
Q

Advantages of capillary electophoresis?

Can combine with what other test to ID proteins?

A

Small volumes, continuous sampling, automation

Proteins seperate by charge and generate a “virtual gel”

Mass spec!

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11
Q

Mass spec:
Weak ionization vs strong and what are they used for?

A

Weak: Same charge on each molecule, seperates on mass, good for mixtures

Strong: Fragments and produces specific fragment

Can combine them

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12
Q

3 types of radioactivity, measured?

Half-life equation?

A

Alpha: He nucleus, low energy, short penetrance

Beta-particles: electrons or positrons: moderate energy, Scintillation (NI or 2,5 phenyl oxazole)

Gamma-rays: High energy photons, gas filled tubes ionized and current measured

0.693/lambda=half-life lambda=specific decay constant

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