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Margatoxin
?99%, recombinant, expressed in E. coli. Group: Fluorescence/luminescence spectroscopy.
Marine venom from Chrysaora quinquecirrha (Sea Nettle)
recombinant, expressed in E. coli, ?80% (SDS-PAGE), buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy.
MDM2 Inhibitor VII, MEL23
The MDM2 Inhibitor VII controls the biological activity of MDM2. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Group: Fluorescence/luminescence spectroscopy.
Medium 199
10 ×, With Hanks? salts, without L-glutamine and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy.
MEG-1 Active human
recombinant, expressed in E. coli, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy.
MEG-2 Active human
recombinant, expressed in E. coli, ?70% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy.
A hormone that has been postulated as the mediator of photo-induced anti-gonadotropic activity in photoperiodic mammals. Group: Fluorescence/luminescence spectroscopy.
Meloxicam - CAS 71125-38-7
A cell-permeable, non-steroidal anti-inflammatory drug (NSAID) of the oxicam family which preferentially inhibits the inducible isoform of COX-2 (IC?? = 4.7 μM) relative to COX-1 (IC?? = 36.6 μM). Group: Fluorescence/luminescence spectroscopy.
A cell-permeable anticancer drug that inhibits the catalytic activity of topoisomerase II (topo II) without damaging DNA or stabilizing DNA-topo II cleavable complexes. Group: Fluorescence/luminescence spectroscopy.
Meriolin 2
Meriolin 2 primarily used in Inhibition. Group: Fluorescence/luminescence spectroscopy.
Meriolin 3 - CAS 954143-48-7
A cell-permeable, ATP site-targeting azaindolopyrimidine compound that is reported to inhibit kinase activity. Group: Fluorescence/luminescence spectroscopy.
Mer RTK Inhibitor, UNC569
Mer RTK Inhibitor, UNC569, 1350547-65-7 is a potent, reversible and ATP-competitive inhibitor of Mer receptor tyrosine kinase (IC50 = 2.9 nM; Ki = 4.3 nM). Group: Fluorescence/luminescence spectroscopy.
meso-Tetraphenylporphyrin
BioReagent, suitable for fluorescence, ?99.0% (HPLC). Group: Fluorescence/luminescence spectroscopy.
Met30 Antagonist, SMER3
The Met30 Antagonist, SMER3 controls the biological activity of Met30. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. Group: Fluorescence/luminescence spectroscopy.
A decapeptide with C-terminally amidated LRF-motif that acts as a potent and selective agonist of AXOR12 and hOT7T175 (a novel human G-protein-coupled receptors). Group: Fluorescence/luminescence spectroscopy.
Met/Flt-3/VEGFR2 Tyrosine Kinase Inhibitor - CAS 888719-03-7
The Met/Flt-3/VEGFR2 Tyrosine Kinase Inhibitor controls the biological activity of Met/Flt-3/VEGFR2 Tyrosine Kinase. Primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy.
Methanol-13C,d4
99.5 atom % D, 99 atom % 13C. Group: Fluorescence/luminescence spectroscopy.
The Met Kinase Inhibitor, also referenced under CAS 658084-23-2, controls the biological activity of Met Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy.