Examples of 'control antibodies' in a sentence
Meaning of "control antibodies"
Control antibodies: Antibodies used in experiments to ensure that any observed effects are due to the target antigen and not other factors
How to use "control antibodies" in a sentence
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control antibodies
Isotype control antibodies show no significant cytotoxicity.
Control samples were incubated with control antibodies.
Wells containing control antibodies served as negative controls.
Separate aliquots were admixed with control antibodies.
Control antibodies were also negative for peptide binding.
Cetuximab was comparable to the bivalent parental control antibodies.
Isotype matching control antibodies were used as negative controls.
Instrument settings were determined by analysis of relevant isotype control antibodies.
Isotype control antibodies had no effect in these assays.
Gates were set based on isotype control antibodies as background.
Control antibodies were of the same isotype as the test antibodies.
The filled portions indicate the isotype control antibodies.
Isotype control antibodies used for each of the antibodies.
Preparation of control antibodies.
Isotype control antibodies are used to control for background fluorescence.
See also
Thresholds for positives were set using isotype matched control antibodies.
Isotype matched control antibodies were used under identical conditions.
Control hESC were stained with the respective isotype control antibodies.
Isotype snatched control antibodies were treated under identical conditions.
The negative control used was cells supplemented with isotype control antibodies.
Isotype matched control antibodies were treated under identical conditions.
The researchers also looked at genes that control antibodies linked to allergies.
Species matching control antibodies of irrelevant specificity were used as negative controls.
No inhibition effect is observed for the control antibodies in the two experiments.
Treatment with monoclonal antibodies according to the invention or isotype control antibodies.
The control antibodies conferring apoptosis already in solution where even more efficient.
The negative control used was cells treated with isotype control antibodies.
The parental antibodies and negative control antibodies were included in these sets of experiments.
Spectral overlap was corrected by appropriate compensation and gates were set using isotype control antibodies.
Cells stained with primary conjugated isotype control antibodies are used to determine background fluorescence.
Replicate tubes were incubated with the corresponding single color and negative control antibodies.
No antibody controls and isotype control antibodies are shown in the first and second columns.
Primary antibodies are used then appropriate species and chain specific control antibodies should be used.
The binding of the test and control antibodies was determined using the Median Fluorescence value.
Background staining observed with the relevant isotype control antibodies has been subtracted.
Isotype-matched control antibodies were used under the same conditions.
Cytochrome conjugate normal mouse immunoglobulins were used as control antibodies to set the gates.
Therapeutic or control antibodies were given 4 h prior to the application of the irritant.
Background staining observed with the relevant isotype control antibodies have been subtracted.
Appropriate control antibodies are also selected, including an irrelevant antibody as negative control.
The dotted lines in each histogram represent background fluorescence after staining with negative control antibodies.
Suitable buffers, control antibodies or probes.
Quadrants were defined using non-relevant isotype matched control antibodies.
Table 1 describes the test and control antibodies administered in this study.
Murine and human IgG1 antibodies were used as isotype control antibodies.
For negative controls, isotype control antibodies or serum from unimmunized animals were used.
X-axis represent the concentration of the test and negative control antibodies.
In some further embodiments, one or more control antibodies are also attached to the substrate.
As a negative control, cells were stained with appropriate isotype matched control antibodies.
In contrast, isotype control antibodies did not impact the number of live cells after treatment.
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