4-Nitrophenyl phosphate bis(cyclohexylammonium) salt has been used as a component in the colorimetric reagent for abscisic acid (ABA) assay.[1][2]
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p-Nitrophenyl phosphate (pNPP) is the preferred substrate for use with alkaline phosphatase in enzyme-linked immunosorbent assay (ELISA) procedures. Due to its high sensitivity, pNPP is the considered substrate in alkaline phosphatase systems. ELISA applications based on pNPP can be read in timed assays or delayed readings by stopping with alkaline solutions. This substrate yields a yellow-colored soluble end product that can be measured spectrophotometrically at 405 nm.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 35(6), e21551-e21551 (2021-05-28)
Intestinal epithelial cells (IEC) are crucial for maintaining proper digestion and overall homeostasis of the gut mucosa. IEC proliferation and differentiation are tightly regulated by well described pathways, however, relatively little is known about how cytokines shape these processes. Given
Abscisic acid synthesis in Acer rubrum L. leaves?a vapor-pressure-deficit-mediated response
World journal of stem cells, 6(4), 497-504 (2014-09-27)
To compare seven commercially available bone graft substitutes (BGS) in terms of these properties and without using any additional biological growth factors. Porcine osteoprogenitor cells were loaded on seven commercially available BGS and allowed to proliferate for one week followed
Leaf abscisic acid accumulation in response to substrate water content: Linking leaf gas exchange regulation with leaf abscisic acid concentration
Biochemistry and biophysics reports, 24, 100830-100830 (2020-10-27)
Para-nitrophenyl phosphate, the common substrate for alkaline phosphatase (AP), is available as a cyclohexylamine salt. Here, we report that cyclohexylamine is a non-competitive inhibitor of APs. Cyclohexylamine inhibited four different APs. Co-crystallization with the cold-active Vibrio AP (VAP) was performed
NBT-BCIP substrate system aids in western blotting and immunohistological staining, producing a blue-purple insoluble end product.
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