Examples of 'anti-rabbit' in a sentence
Meaning of "anti-rabbit"
anti-rabbit (adjective): The term 'anti-rabbit' is used in the context of immunology to describe antibodies that are directed against rabbit immunoglobulins or antigens
How to use "anti-rabbit" in a sentence
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anti-rabbit
The secondary antibody is goat anti-rabbit IgG.
Binding was detected by anti-rabbit antibody alkaline phosphatase conjugate.
Anti-rabbit platelet antiserum was used to induce thrombocytopenia in rabbits.
Horseradish peroxidase is conjugated chemically to goat anti-rabbit immunoglobulin.
The secondary antibody was goat, anti-rabbit IgG conjugated to horseradish peroxidase.
Detection is performed using alkaline phosphatase-conjugated anti-rabbit antibody.
The secondary antibody was a goat anti-rabbit fluorescein conjugated antibody.
Immunostaining was performed using a horseradish peroxidase-coupled anti-rabbit antibody.
Both filters were developed using anti-rabbit IgG labelled with alkaline phosphatase.
Bound antibody molecules were detected using peroxidase-labeled anti-rabbit antibody.
Bound PAb were visualized with anti-rabbit immunoglobulins conjugated with alkaline phosphatase.
Anti-rabbit biotin conjugate and streptavidinalkaline phosphatase were used for color development.
Reactive primary antibody was detected by a secondary anti-rabbit antibody conjugated to horseradish peroxidase.
Visualization was achieved through autoradiographic detection of a chemiluminescent reactive secondary \ goat anti-rabbit antibody.
The detection was by goat anti-rabbit IgG-horse radish peroxidase followed by substrate.
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A very faint signal was barely detectable at the goat anti-rabbit antibody bar.
Incubate with goat anti-rabbit IgG and wash with same buffer.
Rabbit IgG was detected by the addition of a peroxidase conjugated goat anti-rabbit antibody.
Bound antibodies were detected with an anti-rabbit secondary antibody conjugated with alkaline phosphatase.
Slides were then washed as before and incubated with biotinylated goat anti-rabbit antibody.
The secondary antibody was goat anti-rabbit IgG which was conjugated with alkaline phosphatase.
Bound rabbit antibody was then detected by the use of a horseradish peroxidase-labeled anti-rabbit antibody.
The mixtures were then washed and a goat anti-rabbit IgG antibody coupled to fluorescein was added.
In that case, the secondary specific binding partner can be goat anti-rabbit IgG antibody.
The control zone comprised goat anti-rabbit IgG at a similar concentration in the same buffer.
The cells were then washed and stained with fluorescein-conjugated goat anti-rabbit IgG.
Anti-lipolase immunoglobulins were detected using anti-rabbit immunoglobulin antibodies labelled with horseradish peroxidase.
Visualization was achieved through autoradiographic detection of a chemiluminescent reactive secondary HRP-conjugated goat anti-rabbit antibody.
A control line is established by striping goat anti-rabbit IgG on the surface of the pad.
Diluted goat anti-rabbit antibody, the secondary antibody dilution was adapted according to the background levels.
The antibody-bound cAMP was then captured by anti-rabbit IgG coated assay particles.
An anti-rabbit secondary antibody conjugated with TRITC was used for the detection.
Anti-lipase immunoglobulins were detected using anti-rabbit immunoglobulin antibodies labelled with horseradish peroxidase.
A MAb anti-rabbit IgG HRPO conjugate is used to detect IgG bound to the virus.
The amounts of residual rabbit antiserum was detected by pig anti-rabbit immunoglobulin, horshraddish peroxidase labelled.
Bound IgG was quantified by ELISA with peroxidase conjugated goat anti-rabbit Ig.
The bound rabbit antibodies were quantified using anti-rabbit enzyme-conjugated secondary antibody and a colorimetric detection.
Immunoreactive bands were visualised by chemiluminescence using horseradish peroxidase-conjugated anti-rabbit IgG and ECL reagent.
Remove unbound Goat anti-rabbit antibody by inverting plate to remove liquid.
Cell-bound primary antibodies were revealed by secondary swine anti-rabbit IgG labeled with colloidal gold.
Visualisation done by Goat anti-Rabbit immunoglobulins and horseradish peroxidase labelled dextran polymer.
The ELISA was developed using HRP-conjugated goat anti-rabbit polyclonal antibodies.
Goat anti-rabbit antibody coupled to horse radish peroxidase is obtained from Sigma Chemical.
After washing the filter, the blot was incubated with anti-rabbit antibody conjugated with alkaline phosphatase.
Anti-rabbit IgG-HRP conjugate was used as secondary antibody.
Immunoblots were developed using anti-rabbit IgG-alkaline phosphatase conjugate and BCIP.
The secondary antibody was a FITC-conjugated goat anti-rabbit antibody.
Adsorption of Anti-Mouse IgG and Anti-Rabbit IgG Antibodies to Sulfate FluoSpheres.
Then, the blots were revealed after incubation with an HRP-conjugated anti-rabbit antibody.
The membrane was subsequently incubated with a mouse anti-rabbit secondary antibody coupled to alkaline phosphatase ( Promega ).
