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Allophycocyanin clone zet

Manufactured by BioLegend

Allophycocyanin clone ZET is a fluorescent protein used in flow cytometry and other immunoassays. It is derived from a cyanobacterial light-harvesting protein and emits light in the far-red/near-infrared spectrum.

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2 protocols using allophycocyanin clone zet

1

Visualizing IFN-γ-Induced Cells in Spleens

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Spleens from immunized and control IL-27p28–eGFP transgenic mice were removed 6 h after polyIC administration and immediately fixed overnight using PLP buffer, as previously described (30 (link)). Spleens were flash frozen with liquid nitrogen in OCT and 20-μm tissue sections were obtained using a cryostat. Sections were left to dry for 30 min, blocked with 5% BSA for 1 h, and stained with anti-eGFP (Alexa Fluor 488 Rabbit polyclonal; Life Technologies), XCR1 (allophycocyanin clone ZET; BioLegend), and B220 (PE RA3-6B2; BioLegend) in 5% BSA. After washing extensively, sections were coverslipped with Fluoromount mounting medium and left to dry overnight. Slides were imaged on a Zeiss LSM 780 confocal microscope, and image analysis was performed with Fiji (31 (link)).
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2

Visualizing IFN-γ-Induced Cells in Spleens

Check if the same lab product or an alternative is used in the 5 most similar protocols
Spleens from immunized and control IL-27p28–eGFP transgenic mice were removed 6 h after polyIC administration and immediately fixed overnight using PLP buffer, as previously described (30 (link)). Spleens were flash frozen with liquid nitrogen in OCT and 20-μm tissue sections were obtained using a cryostat. Sections were left to dry for 30 min, blocked with 5% BSA for 1 h, and stained with anti-eGFP (Alexa Fluor 488 Rabbit polyclonal; Life Technologies), XCR1 (allophycocyanin clone ZET; BioLegend), and B220 (PE RA3-6B2; BioLegend) in 5% BSA. After washing extensively, sections were coverslipped with Fluoromount mounting medium and left to dry overnight. Slides were imaged on a Zeiss LSM 780 confocal microscope, and image analysis was performed with Fiji (31 (link)).
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