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Hank s buffered salt solution

Manufactured by Corning

Hank's Buffered Salt Solution is a commonly used buffer solution in cell culture and biological research. It is a balanced salt solution that provides a physiologically relevant environment for cells and tissues. The solution contains a mixture of inorganic salts, including sodium chloride, potassium chloride, calcium chloride, and magnesium chloride, as well as a buffering agent to maintain a stable pH.

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2 protocols using hank s buffered salt solution

1

Cell Culture of Prostate Cancer Lines

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LNCaP and C4-2 cells were obtained from the American Type Tissue Collection (ATCC) (Rockville, MD). Cells were grown in RPMI 1640 media (Corning, Manassas, VA) containing either 10% fetal bovine serum (Gemini Bio-Products, West Sacramento, CA) or 10% charcoal stripped fetal bovine serum (HyClone, Logan, UT and Sigma, St. Louis, MO) and supplemented with Ciprofloxacin Hydrochloride 5μg/ml (US Biological, Swampscott, MA), and Gentamicin 50 μg/ml (Quality Biological Inc., Gaithersburg, MD). The cells were passaged in uncoated filter top polystyrene flasks (Corning) and were maintained at 37°C in 5% CO2 in humidified air. Cells were typically split at 80% confluency using 0.05% trypsin (cat # 25-052-CI; Corning) in calcium-free Hank's Buffered Salt Solution (Corning).
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2

Dorsal Root Ganglion Neuron Isolation

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For each tissue preparation, two age- and sex-matched mice were killed by live decapitation, and cervical through lumbar DRG were removed and pooled together. DRG were incubated in papain (45 U, Worthington) for 20 min at 37°C, 5% CO2. DRG were then rinsed and incubated in collagenase (1.5 mg/mL, Sigma-Aldrich) for 20 min. Both enzyme solutions were made up in Ca2+- and Mg2+-free Hanks’ buffered salt solution (Corning) with 10 mm Hepes (Sigma-Aldrich). DRG were manually triturated with fire-polished Pasteur pipettes (VWR) to dissociate neurons, passed through a 40-μm filter (VWR), and plated onto poly-d-lysine/collagen (Sigma-Aldrich)-coated 12-mm glass coverslips (Thermo Fisher Scientific). Neurons were maintained in culture for 2 d in Neurobasal A medium (Invitrogen) supplemented with 100 U/mL penicillin/streptomycin (Corning), 2 mm GlutaMAX (Life Technologies), 2% B27 (Gibco), and 5% fetal bovine serum (Gibco).
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