Laboratory Operations Flashcards
How should an optimal positive control be produced?
In the exact same conditions as the patient tissue (fixation, processing, staining) and cut onto the same slide.
How can you validate a prediluted Ab?
By performing a serial dilution (1:2, 1:4, 1:8 and 1:16) and assessing for reactivity on known positive tissue.
What is the one prediluted Ab that can be run without additional lot validation?
FDA approved pre diluted Ab.
What is a concentrated Ab?
A non-diluted Ab in which several serial dilutions must be performed in order to find the optimal dilution. Called “prep kits” in Vancouver.
Are diluted or concentrated Ab more practical?
Concentrated. Even though the dilution process takes longer, they are much more shelf stable and are much cheaper than diluted Ab. Concentrated Ab also give the user much more control over Ab expression in patient tissue.
What does a 1:20 diluted Ab entail?
1 part Ab, 19 parts diluent totaling up to 20 parts.
What is a lambda in reference to measurement?
An old fashioned way to say microliter. Same as micron=-micrometer.
Why is Ab validation important.
To establish a standardized protocol also to assist with lab reproducibility and consistency.
An appropriate immunohistochemical reaction is dependent upon:
A. incubation time
B. incubation temperature
C. antibody dilution
D. All of the above
D. All of the above.
What is the antibody class most frequently demonstrated in immunofluorescent and immunoenzyme staining?
IgG. Of the immunoglobulin classes, IgG is found most abundantly in serum and consequently most antibodies produced belong to this class.
Polyclonal antibodies are produced by injection of antigen into:
Animals. Specialized cell cultures can be used to produce monoclonal antibodies. Bacterial cultures will not produce antibodies.
What is the chemical used to quench endogenous alkaline phosphatase in tissue sections?
Levamisole. The anti-helminthic drug, levamisole, is effective in quenching non-intestinal alkaline phosphatase.
What is a “checkerboard” titration of primary vs. secondary antibodies is used to determine?
The optimal combination of concentrations of each antibody. It is done by varying the secondary antibody concentration for each of several primary antibody concentrations. When charted out, the results form a grid, or “checkerboard” pattern.
An immunoglobulin molecule can be divided into two fragments known as the antigen-binding fragment (Fab) and the crystalizable fragment (Fc). What is the function of the crystalizable fragment?
To be involved in biologic functions other than antigen binding. The crystalizable fragment of an immunoglobulin molecule is involved in a variety of non-antigen binding biologic functions that are part of the hosts immune response
What are the two principal defense mechanisms of the body’s immune system?
humoral and cell-mediated
With regard to the avidin-biotin- complex (ABC) immunohistochemistry method:
A. the primary antiserum is avidin-labeled
B. no conjugation steps are involved
C. the ABC complex binds to biotin-labeled secondary antibody
D. bridging antiserum is added in excess
C. The ABC complex binds to the biotin-labeled (biotinylated) secondary Ab.
In order to assess the effects of over-fixation and the potential need for antigen retrieval on a given specimen, the inclusion of an antibody against what ubiquitous intermediate filament is suggested in all initial antibody panels?
Vimentin.
Polyclonal antibody serum often labels non-specific antigens in the tissue because:
Polyclonal antiserum contains many Ab.
Where do B cells mature?
The bone marrow.
Which of the cells is responsible for immunoglobulin production?
Plasma cells.