Tetrabenazine-d6 Reference: 26811-10 An internal standard for the quantification of tetrabenazine by GC- or LC-MS
8-DY547-cGMP Reference: 10010109-50 A fluorescently-labeled cyclic nucleotide to study cyclic nucleotide-gated A2 channel activation; opens the channel in a rapid and reversible manner with efficiency equal to cGMP
cis-9,10-Methyleneoctadecanoic acid more than 80%, 1 g Reference: 11-1839-80-13 Synonyms: Dihydrosterculic acid; 8-(2-octylcyclopropyl)octanoic acid
Tetrabenazine-d6 Reference: 26811-5 An internal standard for the quantification of tetrabenazine by GC- or LC-MS
Ptd(S)Ins-(3,4)-P2 (1,2-dipalmitoyl) (sodium salt) Reference: 10010112-1 Ptd(S)Ins-(3,4)-P2 (1,2-dipalmitoyl) is an analog of naturally occurring PtdIns-(3,4)-P2 that contains sulfur rather than oxygen at the sn-3 position of the glycerol backbone. Potential hydrolysis by PLC would yield a free thiol which could then react with chromogenic reagents such as DTNB (Ellman’s reagent). There are no published reports on the biological activity of Ptd(S)Ins-P2(1,2-dipalmitoyl) or its use as a chromogenic substrate for PLC.
9(R),10(S)-Methyleneoctadecanoic acid , mg Reference: 11-1841 Synonyms: Dihydrosterculic acid (synthetic); Methyl cis-9,10-methyleneoctadecanoate
Tetrabenazine-d6 Reference: 26811-500 An internal standard for the quantification of tetrabenazine by GC- or LC-MS
Ptd(S)Ins-(3,4)-P2 (1,2-dipalmitoyl) (sodium salt) Reference: 10010112-100 Ptd(S)Ins-(3,4)-P2 (1,2-dipalmitoyl) is an analog of naturally occurring PtdIns-(3,4)-P2 that contains sulfur rather than oxygen at the sn-3 position of the glycerol backbone. Potential hydrolysis by PLC would yield a free thiol which could then react with chromogenic reagents such as DTNB (Ellman’s reagent). There are no published reports on the biological activity of Ptd(S)Ins-P2(1,2-dipalmitoyl) or its use as a chromogenic substrate for PLC.
9(R),10(S)-Methyleneoctadecanoic acid , 5 mg Reference: 11-1841-4 Synonyms: Dihydrosterculic acid (synthetic); Methyl cis-9,10-methyleneoctadecanoate