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Anti mouse il 12 p40

Manufactured by BioXCell

Anti-mouse IL-12 p40 is a lab equipment product that targets the p40 subunit of the interleukin-12 (IL-12) cytokine in mouse samples. It is used for the detection and quantification of IL-12 p40 in various biological applications.

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2 protocols using anti mouse il 12 p40

1

Quantification of IL-12 and IFN-γ in LLC Tumors

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LLC tumor tissue sections were prepared as previously described (Oh et al., 2017 (link)). Briefly, tumor tissues were fixed in 2% paraformaldehyde overnight, followed by embedding in optimum cutting temperature (O.C.T.; Tissue-Tek) compound, and were cut into 14-μm sections. The sections were blocked with 1.0% BSA in PBST (PBS+ 0.1% Tween 20) and incubated with anti-mouse IL-12 p40 (Bio X Cell) or anti-mouse IFN-γ (Bio X Cell) at room temperature for 1 hr. After wash 3 times with PBST, the sections were stained with goat anti-rat IgG H&L (Alexa Fluor® 568) at room temperature for 1 hr. The sections were next counterstained with DAPI and mounted on glass slides. Images were acquired with a LSM880 microscope with Airyscan and FAST Airyscan High Resolution and 32-channel spectral detectors. Relative fluorescence intensity of IL-12 or IFN-γ was quantified by normalizing integrated fluorescence intensity of IL-12 or IFN-γ to the total cell numbers of macrophages, DCs, or CD8+ T cells per mg of tumor.
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2

Quantification of IL-12 and IFN-γ in LLC Tumors

Check if the same lab product or an alternative is used in the 5 most similar protocols
LLC tumor tissue sections were prepared as previously described (Oh et al., 2017 (link)). Briefly, tumor tissues were fixed in 2% paraformaldehyde overnight, followed by embedding in optimum cutting temperature (O.C.T.; Tissue-Tek) compound, and were cut into 14-μm sections. The sections were blocked with 1.0% BSA in PBST (PBS+ 0.1% Tween 20) and incubated with anti-mouse IL-12 p40 (Bio X Cell) or anti-mouse IFN-γ (Bio X Cell) at room temperature for 1 hr. After wash 3 times with PBST, the sections were stained with goat anti-rat IgG H&L (Alexa Fluor® 568) at room temperature for 1 hr. The sections were next counterstained with DAPI and mounted on glass slides. Images were acquired with a LSM880 microscope with Airyscan and FAST Airyscan High Resolution and 32-channel spectral detectors. Relative fluorescence intensity of IL-12 or IFN-γ was quantified by normalizing integrated fluorescence intensity of IL-12 or IFN-γ to the total cell numbers of macrophages, DCs, or CD8+ T cells per mg of tumor.
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