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Assays were performed in 25 mM HEPES, pH 7.5, 200 mM NaCl, 5 M PLP, 10 mM glutathione and 10 M AzMC, with 0.01% triton-x 100, in 384-well black plates, as a final assay volume of 50 l

ER was isolated from SLC33A1 -knockout HEK293T cells expressing SLC33A1 cDNAs or a vector control treated with 1 mM BSO for 48 h before ER isolation

Chen B, Zhang L, Chen G (2011) Determination of salidroside and tyrosol in Rhodiola by capillary electrophoresis with graphene/poly(urea-formaldehyde) composite modified electrode

Physiological regulation of intestinal epithelial tight junctions as a consequence of Na + -coupled nutrient transport