HL - 60 cells were stained with 1 µg / mL ab14715 (blue) or an equal amount
of an isotype control antibody (red) and analyzed by flow cytometry.
Not exact matches
Use negative
controls (unstained and
isotype control antibodies) to determine gating
of populations.
(d) Histogram
of membrane - bound Tie2 expression in HUVEC and BP compared to
isotype control measured by flow cytometry.
(C) Survival
of gp33 - immunized mice with LCMV infection following 30 d rest period compared with
control mice with ST2 blockade or
isotype control Ab treatment.
They were then washed in FACS buffer I and probed in FACS buffer I containing a 1:500 dilution
of r - phycoerythrin - conjugated goat anti-mouse IgG (Caltag Laboratories, Carlsbad, CA) or an appropriate
isotype control for 15 min in the dark at 4 °C.
Inhibition
of cell proliferation (B)
of MCF7, MCF7 / HER2, or BT474 cells treated for 6 days with F3 - IgG, trastuzumab, or
isotype control antibody.
An isotyping ELISA was performed by coating a 96 - well plate with 1.25 ug / mL
of the IgG1
Isotype Control Antibody and detecting with Alexa Fluor conjugates specific to mouse IgG1, IgG2a, IgG2b, IgG3, IgM and heavy and light chains (H&L)
of IgG.
To assess the ability
of F3 - IgG to inhibit the proliferation
of HER2 - overexpressing breast carcinoma cells, we measured the proliferation
of BT474, MCF7 / HER2 and MCF7 breast cancer cell lines in the presence
of trastuzumab, F3 - IgG, or an
isotype - matched
control antibody.