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Elisa max standard set mouse il 1β kit

Manufactured by BioLegend
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The ELISA MAX Standard Set Mouse IL-1β kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) used for the measurement of mouse interleukin-1 beta (IL-1β) in biological samples. The kit includes all the necessary reagents and components to perform the assay.

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Lab products found in correlation

Human il1β, by PerkinElmer (2 mentions)

Close spelling variants of this product

ELISA MAX sets Mouse IL-1β ELISA MAX kits IL-1β Mouse ELISA kits ELISAs

2 protocols using elisa max standard set mouse il 1β kit

1

Cytokine Quantification in Treated Cells

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Supernatant from treated cells were collected and frozen at −80 °C before determining cytokine concentrations. mIL-1β was determined by ELISA MAX Standard Set Mouse IL-1β kit (BioLegend# 432601). Human IL-1β and IL-18 were determined with Cisbio HTRF Cisbio Human IL1β (#62HIL1BPET) and Human IL18 (#62HIL18PEG) protocols. All the data were from 3 or 4 independent biological replicates.
Wang L., Shi S., Unterreiner A., Kapetanovic R., Ghosh S., Sanchez J., Aslani S., Xiong Y., Hsu C.L., Donovan K.A., Farady C.J., Fischer E.S., Bornancin F, & Matthias P. (2024). HDAC6/aggresome processing pathway importance for inflammasome formation is context-dependent. The Journal of Biological Chemistry, 300(2), 105638.
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2

Cytokine Quantification in Treated Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Supernatant from treated cells were collected and frozen at −80°C before determining cytokine concentrations. mIL-1β was determined by ELISA MAX™ Standard Set Mouse IL-1β kit (BioLegend# 432601). Human IL-1β and IL-18 were determined with Cisbio HTRF Cisbio Human IL1β (#62HIL1BPET) and Human IL18 (#62HIL18PEG) protocols. All the data were from 3 or 4 independent biological replicates.
Wang L., Unterreiner A., Kapetanovic R., Aslani S., Xiong Y., Donovan K.A., Farady C.J., Fischer E.S., Bornancin F, & Matthias P. (2023). HDAC6/aggresome processing pathway importance for inflammasome formation is context dependent. bioRxiv.
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