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3 protocols using mouse antihuman igg fc antibody

1

Spatial Profiling of T-DM1 Distribution in Tumors

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As
previously described,18 (link),21 (link) the tumor distribution of T-DM1-AF680
was analyzed using fluorescence microscopy at 1, 3, 5, and 7 days.
Briefly, nude mice were inoculated with 5 × 106 NCI-N87
cells in the rear flanks and the clinical dose (3.6 mg/kg) of T-DM1-AF680
was administered via tail-vein injection once the longest axis of
the tumor was approximately 10–12 mm. Before euthanizing mice
at the aforementioned times, Hoechst 33342 (ThermoFisher Scientific,
H3570) was administered via the tail-vein at 15 mg/kg to label functional
vasculature in the tumor.31 (link) After euthanizing
the mice, tumors were resected, flash frozen in OCT using isopentane
chilled on dry ice, and cut for histology on a cryostat (16-μm
slices). Before imaging, slices were stained with antimouse CD31 (BioLegend,
102402) conjugated with Alexa Fluor 555, and mouse antihuman IgG Fc
antibody (BioLegend, 409302) conjugated with Alexa Fluor 488. Microscopy
was performed using an upright Olympus FV1200 confocal microscope
equipped with a 20× objective and 405, 488, 543, and 635 lasers
(Figure S5). Tumor images were obtained
by stitching smaller images with the Olympus software. Images were
exported and analyzed using ImageJ image analysis software as described
previously.18 (link),21 (link)
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2

ELISA for Trastuzumab and Bevacizumab

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Immulon IV 96 well plates (Fisher
Scientific, 14-245-153) were coated with mouse antihuman IgG Fc antibody
(BioLegend, 409302) overnight at 4 °C and 1 μg/mL in PBS.
Wells were then washed 3 times (PBS with 0.05% Tween-20), blocked
with 2% PBS-BSA, 0.05% Tween-20 for 2 h at room temperature, and washed
3 more times. Samples were diluted at least 1:100 in diluent (PBS,
1% BSA, 0.05% Tween-20) and incubated for 1 h at room temperature.
After sample incubation, plates were washed 3 times, and the detection
antibody, mouse antihuman IgG Fc HRP (Southern Biotech, 9040-05),
was diluted 1:10000 in diluent, added to each well, and incubated
for 1 h at room temperature. Plates were then washed 4 times and developed
using TMB substrate (Fisher Scientific, ENN301). Assay ranges for
both trastuzumab and bevacizumab were between 6 ng/mL and 1.2 μg/mL.
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3

Labeling Antibodies and ADCs for Imaging

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Herceptin (trastuzumab, Roche) and Kadcyla (T-DM1, Roche) were obtained from the University of Michigan Pharmacy. Alexa Fluor 680 NHS Ester (AF680, ThermoFisher Scientific, A37567), IRDye 800CW NHS Ester (IRDye, LI-COR, 929-70020), and CellTrace™ Far Red DDAO-SE (DDAO, ThermoFisher Scientific, C34553) were conjugated to the antibodies following the manufacturer's instructions as previously described(15 (link),16 (link)). Antibody/ADC at 2mg/mL supplemented with 10% sodium bicarbonate (v/v) was reacted with dye at molar ratios of 0.5 (AF680, IRDye) and 1.5 (DDAO) for 2 hours at room temperature and purified using P6 Biogel (1g gel/10mL PBS) resulting in dye to protein ratios of approximately 0.3 (AF680, IRDye) and 0.7 (DDAO). Our previous work has shown that the distribution of T-DM1 is unchanged after labeling with AF680 at dye to protein ratio of 0.3 or less(17 (link)). Antibody/ADC dye conjugates were run on SDS-PAGE and scanned on the Odyssey CLx Scanner (LI-COR) to ensure free dye was removed. For fluorescence histology, antimouse CD31 (BioLegend, 102402) was conjugated with Alexa Fluor 555 (ThermoFisher Scientific, A37571), mouse antihuman IgG Fc antibody (BioLegend, 409302) was conjugated with Alexa Fluor 488 (ThermoFisher Scientific, A20000), and trastuzumab was conjugated with Alexa Fluor 750 (ThermoFisher Scientific, A20011) at dye to protein ratios of 1.5.
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