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Invivomab anti mouse ifnγ

Manufactured by BioXCell

InVivoMAb anti-mouse IFNγ is a laboratory product for research purposes. It is a monoclonal antibody that binds to and neutralizes mouse interferon-gamma (IFNγ).

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2 protocols using invivomab anti mouse ifnγ

1

Immune Modulation for Retinal Protection

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I) For CD4+ T cell depletion, intraperitoneal injection of Ultra-LEAF™ Purified anti-mouse CD4 Antibody (10 μg/g, clone GK1.5, BioLegend, San Diego, CA, USA) or corresponding isotype antibody (Ultra-LEAF Purified Rat IgG2b, κ Isotype Ctrl Antibody, clone RTK4530, 10 μg/g, BioLegend) was performed in mice on day 15, 25, and 40 PMI. ii) For CXCR3 blockade, intraperitoneal injection of Ultra-LEAF™ Purified anti-mouse CD183 (CXCR3) Antibody (10 μg/g, clone CXCR3-173, BioLegend) or corresponding isotype antibody (Armenian Hamster IgG, clone: HTK888, BioLegend) was performed in mice every 7 days since day 15 PMI. iii) For systemic IFN-g blocking, mice were injected i.p. with 200 mg of anti-IFN-g antibody (InVivoMAb anti-mouse IFNγ, BioXcell, clone XMG1.2) every 3 days since day 15 PMI. An IgG1 isotype antibody (HRPN, BioXcell) was used to serve as control. iv) To block VCAM-1, a InVivoMAb anti-mouse VCAM-1 (10 mg/kg, BioXcell; corresponding isotype antibody: InVivoMAb rat IgG1 isotype control, clone HRPN, BioXcell) was administrated intravenously in MB-injected mice every 3 days since day 15 PMI. For retinal evaluation in abovementioned in vivo antibody intervention experiments, one retina from each recipient mouse was randomly selected and used for RGC density, while the other was for Iba1 and GFAP staining.
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2

ConA-induced liver injury model

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Concanavalin A (ConA, cat# J61221), purchased from Alfa Aesar (Tewksbury, MA), was dissolved in saline and injected through the lateral tail vein at the dose of 10 mg/kg, except for the survival experiments in which 20 mg/kg was used for the WT and LXRα‐KI mice, and 25 mg/kg was used for the WT and FABP‐VP‐LXRα mice. When necessary, GW3965 was gavaged daily at the dose of 30 mg/kg beginning 3 days before the ConA treatment and until the day of tissue harvest. For in vivo neutralization of IFN‐γ, mice were injected intravenously with 200 μg InVivoMAb anti‐mouse IFN‐γ or the isotype control IgG (see Supporting Table S1) from Bio X Cell (West Lebanon, NH) 1 hour before the ConA injections. Mice were sacrificed at the indicated time points for serum and liver harvest. Blood was collected through cardiac puncture and subsequently centrifuged at 8,000g for 5 minutes to collect the serum. Livers were excised for histology, or they were snap‐frozen on dry ice and stored at −80°C until further analysis.
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