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3.0 mm zirconium beads

Manufactured by Benchmark Scientific
Sourced in United States

The 3.0 mm zirconium beads are a type of laboratory equipment used for various applications. They are composed of zirconium, a durable and chemically resistant material. These beads are designed to provide an efficient means of homogenizing, disrupting, or grinding samples in a variety of laboratory processes.

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2 protocols using 3.0 mm zirconium beads

1

Characterization of Red Leaf Lettuce

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The following standards were purchased: sinapic acid, hippuric acid, caffeic acid, quercetin 3-glucoside (all ≥98% purity, Sigma, St. Louis, MO), chlorogenic acid (primary standard grade, ≥98% purity, Chromadex, Irvine, CA), and cyanidin 3-O-β-glucopyranoside (≥97% purity, Polyphenols, Norway). BeadBug™ Microtube Homogenizer and 3.0 mm zirconium beads were purchased from Benchmark Scientific (Edison, NJ).
RSL looseleaf variety NFR, was provided by Shamrock Seed Co. (Salinas, CA) and green leaf lettuce (GL) variety Crispa (Andy Boy, Salinas, CA) were purchased from the grocery store (Stop and Shop, Highland Park, NJ). NFR plant and seed vouchers were made and deposited at the Chrysler Herbarium and ATCC [4 (link),12 (link)]. Outer leaves and tops of RSL lettuce heads were used as they have the highest levels of phenolics. Lettuce leaves were rinsed, lyophilized and homogenized in a Vitamix Professional 500 Blender (Cleveland, OH) to a fine powder. Dried RSL and GL powders were used for phytochemical extraction, nutritional analyses, and rodent diet formulations.
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2

Cytokine Profiling of Breast Tissue

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Frozen breast tissue was placed into chilled 2-ml homogenization tubes containing 3.0 mm zirconium beads (Benchmark Scientific, Edison, NJ, USA). Cold PBS with 2X complete protease inhibitor cocktail (Roche, Basel, Switzerland) was added in a ratio of 4 μl/mg (tumor) or 3 μl/mg (non-tumor) tissue, and samples were homogenized using a FastPrep-24 5G instrument (MP Biomedicals) with 3 runs of 30 s at 6 m/s. After sequential centrifugation (14,000×g for 15 min at 4 °C, transfer to a new tube, then 14,000×g for 10 min at 4 °C), supernatant aliquots were taken for protein quantification using a BCA assay kit (Thermo Scientific) in accordance with the manufacturer’s protocol. PBS with protease inhibitor was added to normalize the protein concentrations of all supernatant samples to 1.5 mg/ml, and samples were stored at − 80 °C until analysis. Cytokine expression was evaluated using the Human Cytokine/Chemokine Array 65-Plex Assay performed by Eve Technologies (Calgary, AB, Canada). Background fluorescence was subtracted from all samples, and data were log10-transformed prior to further analysis.
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