Chapter 9, 10, 11 Flashcards

1
Q

Serum

A

Liquid portion minus coagulation factors

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2
Q

Plasma

A

Contains all clotting factors

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3
Q

Why are patient samples diluted?

A

To make a less concentrated solution

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4
Q

How can a Complement be inactivated?

A

Heat sample to 56 degrees for 30 min

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5
Q

Volumetric pipette

A

Delivers one volume

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6
Q

Graduated pipette

A

Markings for varying amounts

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7
Q

Micropipettes

A

Delivers small volumes

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8
Q

What do TD & TC stand for?

A

To deliver & To contain

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9
Q

Antibody Titer

A

Measures the concentration of an antibody

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10
Q

What do Acute & Convalescent samples mean?

A

Acute: Still having symptoms & Convalescent: Recovering

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11
Q

Epitope

A

Part of antigen that binds to antibody antigen-binding site

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12
Q

Hapten

A

To small to cause production of antibody by itself

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13
Q

Affinity

A

Initial force of attraction between single antigen-binding site on antibody molecule

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14
Q

Avidity

A

Overall strength of antigen-antibody binding

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15
Q

Define precipitation & agglutination immunoassay

A

Precipitation: Soluble antigen is combined with soluble homozygous
Agglutination: Prevents agglutination

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16
Q

What’s the formula for Precipitation?

A

Soluble = soluble = Insoluble Visable lattice formation

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17
Q

What are 3 zones of precipitation reaction

A

Prozone, Zone of Equivalence, and Post Zone

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18
Q

Where does optimal lattice formation become visible?

A

Zone of equivalence

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19
Q

Immunoturbidimetry

A

Measures reduction in light intensity due to turbidity

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20
Q

Nephelometry

A

Measures light that is scattered at an angle

21
Q

RID

A

Manual, single diffusion technique

22
Q

Ouchterlony

A

Double diffusion technique

23
Q

Identity Pattern

A

Fusion of lines at their junction to form an arc

24
Q

Non-Identity Pattern

A

A pattern of crossed lines

25
Partial Identity Pattern
Fusion of two lines
26
Ring around the Antibody well indicates
Clown looking face
26
Parallel Lines Indicates
Two lines on the side
27
IFE
Double diffusion technique performed to visualize increase or decrease production of antibody class
28
Direct Agglutination
Use particles with naturally occurring antigens
29
Indirect Agglutination
Use particles coated in antigens not normally found
30
Reverse Indirect Agglutination
Antibody attached to the carrier particles
31
Agglutination Inhibition
Based on competition between particulate and soluble antigens
32
What does Hemagglutination Inhibition use?
RBCs
33
Analytical Sensitivity
Ability to detect very small amount of a substance
34
Analytical Specificity
Ability to detect a substance without interference from cross-reactivity substance
35
Analyte
Substance being measured
36
Why use labeled Immunoassays?
They are designed for antigen and antibodies that may be small
37
What type of labels can be used?
Radioactive, Enzyme, Fluorescent, and Chemiluminescent
38
Heterogenous Immunoassays
* More sensitive of the two * Requires physical separation
39
Homogenous Immunoassays
Doesn’t require physical separation
40
Competitive Immunoassays
*All reactants are added at the same time *Concentration is inversely proportional to labeled reagent
41
Noncompetitive Immunoassays
Patient analyte is captured by Ab bound to solid phase
42
Heterogenous Immunoassays
*more sensitive of two types of *requires physical separation
43
Homogenous Immunoassays
Doesn’t require physical separation
44
Competitive Immunoassays
*All reactants are added at the same time *Concentration is inversely proportional to labeled reagent
45
Noncompetitive Immunoassays
Concentration is directly proportional to labeled reagent
46
Autoantibodies
Patient Ab produced in vivo that resemble reagent Ab
47
What are Heterophole antibodies?
Antibodies that react to animal protein
48
Cross reactivity
Describes the detection of a substance other than the analyte of interest