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Measurement of H2S content
H2S quantification was performed as described by Nashef
et al. (1977). The chemical treatments were the same as the
measurements of Na+ and K+ contents. Following the treatments,
the root of seedlings were ground into fine powder with
a mortar and pestle under liquid nitrogen and 0.3 g of frozen
tissue were homogenized in 1 ml 100 mM potassium phosphate
buffer (pH 7) containing 10 mM ethylenediaminetetraacetic
acid (EDTA). The homogenate was centrifuged at
15,000¡Ág for 20 min at 4 ¡ãC, and 100 ¦Ìl of the supernatant
was used for the quantification of H2S, in an assay mixture also
containing 1,880 ¦Ìl extraction buffer and 20 ¦Ìl 20 mM 5,5¡ä-
dithiobis (2-nitrobenzoic acid), to a total volume of 2 ml. The
assay mixture was incubated at room temperature for 2 min
and the absorbance was read at 412 nm. H2S was quantified
based on a standard curve of known concentrations of NaHS

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Hydrogen sulfide is involved in maintaining ion homeostasis via regulating plasma membrane Na+/H+ antiporter system in the hydrogen peroxide-dependent manner in salt-stress Arabidopsis thaliana root
Protoplasma (2014) 251:899¨C912
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2Â¥: Originally posted by starseacow at 2015-07-17 21:42:00
Measurement of H2S content
H2S quantification was performed as described by Nashef
et al. (1977). The chemical treatments were the same as the
measurements of Na+ and K+ contents. Following the tr ...

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     ¼Ó0.3 ml f
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5Â¥: Originally posted by Ô°ëÍäÍä at 2015-07-19 11:40:06
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