sodium cacodylate


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so·di·um cac·o·dyl·ate

used in anemia, leukemia, and malaria.
References in periodicals archive ?
Muscle samples were washed in 0.1 M sodium cacodylate buffer, post-fixed in 1% Os[O.sub.4] for 2 h at room temperature, washed again in the same buffer followed by distilled water, contrasted with 5% aqueous uranyl acetate solution for 1 h and finally washed in distilled water (Rocha, Leonardo, De Souza, Palma, Da Cruz-Hofling, 2008; Rocha, Souza, Palma, da Cruz-Hofling, & Harris, 2009).
The roots were immersed in 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer at 4[degrees]C and pH 7.4 for 12 h.
Heads were submersion-fixed in Karnovsky's fixative (2% paraformaldehyde, 2.5% glutaraldehyde, 2.2% sodium cacodylate buffer, pH 7.4).
Cacodylate-HCL buffer (0.2 M): (i) Sodium cacodylate (42.8 g), Distilled water (1000 ml); (ii) 0.2 M HCl - Concentrated HCl 36-38% (10 ml), Distilled Water (603 ml).
After treatment, the parasites were washed with 0.01 M PBS and fixed in 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer for 2 h.
The supernatant was discarded and the masses of conidia fixed in modified Karnovsky fixative, composed of 2.5% glutaraldehyde and 2.5% formaldehyde in 0.05M sodium cacodylate buffer, pH 7.2, plus 0.1M Ca[Cl.sub.2], and kept in the refrigerator for 24h (primary fixation).
Samples were transferred to a 2.5% glutaraldehyde in 0.1M sodium cacodylate buffer at pH 7.4 and stored for 24h at 4[degrees]C for fixation.
Materials: Olive oil was purchased from Olivoila, Itlay, CsA from Novartis, Basel, Switzerland, Araldite resin from Tab Laboratories Equipment LTD, Berkshire, England, and sodium cacodylate and OsO4 were purchased from Sigma, USA.
Tentacles were cut and fixed in a Karnovsky fixative (4% glutaraldehyde 2% paraformaldehyde in 0.1M sodium cacodylate buffer), pH 7.8, at 4[degrees]C overnight, and washed in 0.1 M sodium cacodylate buffer.
Anterior pituitary tissue was cut into about 1-[mm.sup.3] blocks, immediately immersed in precooled fixative (1.5% glutaraldehyde, 0.3% paraformaldehyde, 3 mM Ca[Cl.sub.2], 0.1 M sodium cacodylate buffer), and embedded with Epon LX112 by routine procedures.
Nerve segments were washed with 0.1 M sodium cacodylate, fixed in 2.5% glutaraldehyde, 4% paraformaldehyde, 0.02% picric acid in cacodylate buffer overnight at 4[degrees]C and washed three times with the cacodylate buffer followed by fixation in a solution containing 1% osmium tetroxide and 1.5% potassium ferricyanide for 60 min at room temperature.
The nerve fragments were fixed in solution -2.5 % glutaraldehyde and 4 % paraformaldehyde in 0.1 M sodium cacodylate (Sigma-Aldrich) buffer, ph 7.2--for 24 h at 4 [degrees]C.