Preparation of Holding ACSF (artificial cerebrospinal fluid) for slice electrophysiology

Thomas Hnasko, Sarthak M. Singhal

Published: 2024-01-19 DOI: 10.17504/protocols.io.n92ldm6ool5b/v1

Abstract

Hnasko lab- preparation of Holding ACSF

Holding ACSF is used for incubating brain slices prior to cell-attached or whole-cell electrophysiological recordings of neurons.

Steps

1.

Prepare 10X stock solution.

1.1.

Composition of 1L of 10X Holding ACSF (in mM): 1150 NaCl, 25 KCl, 12.3 NaH2PO4, 100 d-glucose, 20 CaCl2 and 20 MgSO4.

1.2.

Composition of 1L of 10X Holding ACSF (in g): 67.2 NaCl, 1.86 KCl, 1.47 NaH2PO4, 18.02 d-glucose, 2.94 CaCl2 and 4.93 MgSO4.

2.

Dissolve all salts in 1L of ddH2O to make 10X stock solution of Holding ACSF.

3.

Dilute 10X solution to 1X for use in experiments.

3.1.

Dilute 100mL of 10X solution to ~ 800mL with ddH2O and add (in mM): 26 NaHCO3, 2 thiourea, 5 Na-ascorbate and 3 Na-pyruvate; (in g): 2.18 NaHCO3, 0.15 thiourea, 0.98 Na-ascorbate and 0.33 Na-pyruvate.

3.2.

Add ddH2O to final volume of 1L.

4.

Bubble the solution with carbogen (95% O25% CO2) for ~10 minutes.

5.

After bubbling, measure and adjust pH of solution to ~ 7.3 with 12 N HCl (<1 ml).

6.

Refrigerate until use.

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