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Beta mercaptoethanol

Manufactured by Lonza
Sourced in United States

Beta-mercaptoethanol is a reducing agent commonly used in laboratory settings. It is a clear, colorless liquid with a characteristic odor. The primary function of beta-mercaptoethanol is to reduce disulfide bonds in proteins, enabling the denaturation and analysis of protein structures.

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2 protocols using beta mercaptoethanol

1

Investigating Monocyte and Epithelial Cell Responses to Nano-WC–Co Particles

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THP-1 human monocyte cell line (TIB-202) and BEAS-2B cells were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA). Nano-WC–Co composite particles were purchased from Inframat Advanced Materials (Manchester, CT, USA). RPMI-1640 medium for THP-1 cell culture was purchased from ATCC. Phosphate-buffered saline (PBS), Dulbecco’s Modified Eagle’s Medium (DMEM), 0.25% trypsin/ethylenediaminetetraacetic acid (EDTA), versene (EDTA-based cell detachment reagent), penicillin/streptomycin, beta-mercaptoethanol and fetal bovine serum (FBS) were purchased from Lonza (Allendale, NJ, USA). Isopropanol, hydrochloric acid, Triton-X-100, thiazolyl blue tetrazolium bromide (MTT reagent), phorbol-12-mystirate-13-acetate (PMA), LPS and enzyme-linked immunosorbent assay (ELISA) kits for human IL-12 (#RAB0252), IL-10 (#RAB0244), IL-1β (#RAB0273) and TNFα (#RAB0476) were purchased from Sigma-Aldrich (St Louis, MO, USA). Flow cytometry staining buffer (containing 0.2% bovine serum albumin and sodium azide), recombinant human IL-4, human immunoglobulin G (IgG), antihuman CD40-APC and antihuman CD206-FITC antibodies were purchased from BD Biosciences (Franklin Lakes, NJ, USA).
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2

Assessing CLL Cell Viability with PI3Ki

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For viability assays, patient-derived CLL cells were incubated with PI3Ki in an enriched medium containing an insulin/transferrin/selenium supplement plus beta-mercaptoethanol (BioWhittaker) (22 (link)), stained with the SYTOX Dead Cell Stains (Thermofisher) at the indicated timepoints, and then analyzed by flow cytometry. Resultant data were calculated using FlowJo software (FlowJo, LLC). For BMDM-supported CLL-cell survival assays, BMDMs were polarized with 50ng/ml M-CSF for 6 days. After treatment with duvelisib for 1 hour, BMDMs were cultured with M-CSF and IL-4 for 12 hours. Finally, BMDM were added to leukemic B cells at a ratio of 4:1 (monocytes to CLL cells) and CLL-cell viability assessed via Guava ViaCount assay (MilliporeSigma) on days 0 and 5 of culture.
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