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After 60 min incubation the samples were washed 2x with 1 ml of binding buffer (125 mM Tris-HCl (pH = 8.0), 150 mM NaCl, 1 mM EDTA, 1 mM DTT, 0.1% Tween 20), mixed with 1 ug of SNIP1 peptide in 300 ul of binding buffer and rotated for 60 min at 4 C

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It also must not be used for fluid replacement or volume expansion, and not for epidural or spinal anesthesia

These discoveries provide novel therapeutic options for patients with multiple sclerosis, complementing existing immunosuppressive strategies