-
17236-25A ceramide analog that inhibits glucosylceramide synthase with an IC<sub>50</sub> value between 2 and 20 µM.
-
17236-5A ceramide analog that inhibits glucosylceramide synthase with an IC<sub>50</sub> value between 2 and 20 µM.
-
17236-50A ceramide analog that inhibits glucosylceramide synthase with an IC<sub>50</sub> value between 2 and 20 µM.
-
17599-1A stable, cell-permeable tryptophan derivative with an octyl ester protected COOH group.
-
17599-5
Thomas Scientific
DL-Tryptophan octyl ester (hydrochloride)-5 g
Price: $1,429.69List Price: $1,588.55A stable, cell-permeable tryptophan derivative with an octyl ester protected COOH group. -
17599-500
Thomas Scientific
DL-Tryptophan octyl ester (hydrochloride)-500 mg
Price: $227.52List Price: $252.80A stable, cell-permeable tryptophan derivative with an octyl ester protected COOH group. -
11216-100A reagent that reacts with the primary amine group of PE lipids facilitates the use of electrospray tandem MS for the detection of diacyl, ether, and plasmalogen PE lipid.
-
11216-50A reagent that reacts with the primary amine group of PE lipids facilitates the use of electrospray tandem MS for the detection of diacyl, ether, and plasmalogen PE lipid.
-
11216-500A reagent that reacts with the primary amine group of PE lipids facilitates the use of electrospray tandem MS for the detection of diacyl, ether, and plasmalogen PE lipid.
-
11219-1DMABA-d10 NHS ester is intended for use in combination with DMABA NHS ester (Item No. 11216) as a derivatizing reagent for PE lipids in order to facilitate MS characterization and to quantify relative changes in their abundance.
-
11219-10DMABA-d10 NHS ester is intended for use in combination with DMABA NHS ester (Item No. 11216) as a derivatizing reagent for PE lipids in order to facilitate MS characterization and to quantify relative changes in their abundance.
-
11219-5DMABA-d10 NHS ester is intended for use in combination with DMABA NHS ester (Item No. 11216) as a derivatizing reagent for PE lipids in order to facilitate MS characterization and to quantify relative changes in their abundance.