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Meca 367

Manufactured by BioXCell
Sourced in United States

MECA-367 is a robust and versatile laboratory instrument designed for high-throughput analysis. It utilizes advanced spectroscopic techniques to enable precise measurements and data collection. The core function of MECA-367 is to facilitate accurate and efficient sample analysis across a wide range of applications.

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4 protocols using meca 367

1

Trafficking of Naïve T-Cells in Mice

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Naïve OT-I T-cells isolated from pooled LN and spleen of OT-I RAG1−/−/Thy1.1 mice (4×106 cells) or polyclonal CD8+ T-cells pooled from LN and spleen of C57BL/6 mice and depleted of CD44 expressing cells by magnetic beads (Miltenyi) were injected into the lateral tail vein of recipients. In blocking experiments, cells were incubated with 100 ng/mL pertussis toxin (PTX, Sigma) for 1 h at 37°C, or 100 µg of rat IgG (Jackson Immunoresearch), anti-CD62L (Mel-14, ATCC), or anti-CD11a (M17/4, BioXcell), or 50 µg of anti-CCR7 (4B12, eBioscience) and washed before injection. Luminal PNAd or MAdCAM-1 were blocked by injection of 100 µg of anti-MAdCAM-1 (MECA-367, BioXcell), anti-PNAd (MECA-79, BioLegend) or isotype rat IgG or IgM i.v. 1 h prior to T-cell transfer. In some experiments, cells were labeled with Cell Trace Violet (CTV) (Invitrogen) prior to transfer. Tissues were harvested 1 h or 18 h after naïve T-cell transfer.
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2

Optogenetic Colitis Modulation

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ChR2/TH mice and their controls (negative littermates exposed to the light stimulation) were exposed to 3% DSS for 7 days, and 20 min before the daily optogenetic stimulation, they were injected IP with anti-MAdCAM-1 antibody (MECA-367) or an isotype control (100 μg/mouse in saline; BioXcell). Their weights were monitored daily, and at the end of the experiment the mice were sacrificed, and the entire colon was removed from caecum to anus. The colon length was measured as a marker of inflammation, and the tissue was used for histological staining and scoring, and flow cytometry analysis.
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3

Modulating Hepatic Fibrosis in Mice

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To induce hepatic fibrosis, eight-week-old male mice were randomized to receive twice-weekly oral gavage of CCl4 (2 mL/kg CCl4 in 1:1 v/v olive oil) or an equal volume of olive oil for six weeks. After 2 weeks of CCl4 treatment, a randomized cohort of mice received twice-weekly intraperitoneal injections of 8 mg/kg α4β7 mAb (DATK32; Bioxcell, West Lebanon, NH, USA) or MAdCAM-1 mAb (MECA-367; Bioxcell, West Lebanon, NH, USA), or rat IgG2a isotype antibody (Bioxcell, West Lebanon, NH, USA) for four weeks.
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4

Trafficking of Naïve T-Cells in Mice

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Naïve OT-I T-cells isolated from pooled LN and spleen of OT-I RAG1−/−/Thy1.1 mice (4×106 cells) or polyclonal CD8+ T-cells pooled from LN and spleen of C57BL/6 mice and depleted of CD44 expressing cells by magnetic beads (Miltenyi) were injected into the lateral tail vein of recipients. In blocking experiments, cells were incubated with 100 ng/mL pertussis toxin (PTX, Sigma) for 1 h at 37°C, or 100 µg of rat IgG (Jackson Immunoresearch), anti-CD62L (Mel-14, ATCC), or anti-CD11a (M17/4, BioXcell), or 50 µg of anti-CCR7 (4B12, eBioscience) and washed before injection. Luminal PNAd or MAdCAM-1 were blocked by injection of 100 µg of anti-MAdCAM-1 (MECA-367, BioXcell), anti-PNAd (MECA-79, BioLegend) or isotype rat IgG or IgM i.v. 1 h prior to T-cell transfer. In some experiments, cells were labeled with Cell Trace Violet (CTV) (Invitrogen) prior to transfer. Tissues were harvested 1 h or 18 h after naïve T-cell transfer.
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