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Microtube homogenizer

Manufactured by Benchmark Scientific
Sourced in United States

The Microtube homogenizer is a laboratory instrument designed for the efficient homogenization of small sample volumes, typically in the range of 0.2 to 2 milliliters. The device utilizes a high-speed motor to drive a stainless steel shaft and blade assembly, providing thorough mixing and disruption of samples within microtubes or small vials.

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2 protocols using microtube homogenizer

1

Assessing Wound Antioxidant and Lipid Peroxidation

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Wound tissue samples were excised at the size of 1.0 cm × 1.0 cm on day 2 and day 8 post-wounding and biochemically analyzed to estimate endogenous antioxidant enzyme and lipid peroxidation activities. Each tissue sample was dried and weighed prior to use for analysis. Tissues were transferred to a bead tube with Tris-buffer and homogenized using a microtube homogenizer (Benchmark Scientific, USA). The homogenized tissues were then centrifuged at 6000 rpm for 20 min and we collected the supernatant for the biochemical estimations. Activity levels of endogenous antioxidant enzymes such as superoxide dismutase (SOD) (Item No 706002; Cayman) and glutathione peroxidase (GPx) (Item No 703102; Cayman) and lipid peroxidation, measured as malondialdehyde (MDA) content (Item No 10009055; Cayman), were measured following the vendor’s protocol.
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2

Western Blot Analysis of Myelin Basic Protein

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Forebrain tissues, which were dissected from whole brains as described above, were lysed and homogenized in Radio-Immunoprecipitation Assay (RIPA) buffer (Thermo Scientific) supplemented with Complete Mini Proteinase Inhibitor Cocktail Tablets (Roche) using a microtube homogenizer (Benchmark Scientific). Protein samples (50 ug/lane) were separated on 15% Criterion Tris-HCl Precast Gel (BioRad), and Western blotting was performed, as described (Zhu et al., 2013 (link)). The target proteins were probed by anti-MBP (Covance) and anti-p-actin (Sigma) antibodies. p-actin was used as the loading control. Images on blots were detected with Pierce ECL-2 Western blotting substrate (Pierce) in ChemiDoc XRS+ Imaging System (Bio-Rad). Band densitometry was quantitated using BioRad Image Lab 4.1 (Bio-Rad).
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