Name | Description | Size | Catalog # | |
---|---|---|---|---|
Maurotoxin | Maurotoxin activity was extensively assayed on a large array of K+ channel… | 0.5 mg | STM-340 | More Info |
Maurotoxin | Maurotoxin activity was extensively assayed on a large array of K+ channel… | 1 mg | STM-340 | More Info |
Maurotoxin | Maurotoxin activity was extensively assayed on a large array of K+ channel… | 5 mg | STM-340 | More Info |
M8-B hydrochloride | M8-B hydrochloride is a potent and selective blocker of TRPM8 channel, inh… | 10 mg | M-220 | More Info |
M8-B hydrochloride | M8-B hydrochloride is a potent and selective blocker of TRPM8 channel, inh… | 100 mg | M-220 | More Info |
M8-B hydrochloride | M8-B hydrochloride is a potent and selective blocker of TRPM8 channel, inh… | 25 mg | M-220 | More Info |
M8-B hydrochloride | M8-B hydrochloride is a potent and selective blocker of TRPM8 channel, inh… | 5 mg | M-220 | More Info |
M8-B hydrochloride | M8-B hydrochloride is a potent and selective blocker of TRPM8 channel, inh… | 50 mg | M-220 | More Info |
MCD peptide | MCD peptide inhibits KV1.1 and KV1.2 channels1,2. Synthetic peptide. Purit… | 0.5 mg | STM-250 | More Info |
MCD peptide | MCD peptide inhibits KV1.1 and KV1.2 channels1,2. Synthetic peptide. Purit… | 1 mg | STM-250 | More Info |
MCD peptide | MCD peptide inhibits KV1.1 and KV1.2 channels1,2. Synthetic peptide. Purit… | 10 mg | STM-250 | More Info |
MCD peptide | MCD peptide inhibits KV1.1 and KV1.2 channels1,2. Synthetic peptide. Purit… | 5 mg | STM-250 | More Info |
m-Chlorophenylbiguanide hydrochloride | m-Chlorophenylbiguanide is an activator / agonist of 5-HT3 channels1. Synt… | 1 g | M-160 | More Info |
m-Chlorophenylbiguanide hydrochloride | m-Chlorophenylbiguanide is an activator / agonist of 5-HT3 channels1. Synt… | 500 mg | M-160 | More Info |
MCI-225 | MCI-225 shows high affinity for the 5-HT3 receptor, Ki less than 100 nmol… | 10 mg | M-190 | More Info |
MCI-225 | MCI-225 shows high affinity for the 5-HT3 receptor, Ki less than 100 nmol… | 25 mg | M-190 | More Info |
MCI-225 | MCI-225 shows high affinity for the 5-HT3 receptor, Ki less than 100 nmol… | 5 mg | M-190 | More Info |
MCI-225 | MCI-225 shows high affinity for the 5-HT3 receptor, Ki less than 100 nmol… | 50 mg | M-190 | More Info |
MDL 72222 | MDL 72222 is an antagonist of 5-HT3 receptors1. Synthetic. Purity >95%. MW… | 10 mg | M-155 | More Info |
MDL 72222 | MDL 72222 is an antagonist of 5-HT3 receptors1. Synthetic. Purity >95%. MW… | 25 mg | M-155 | More Info |
MDL 72222 | MDL 72222 is an antagonist of 5-HT3 receptors1. Synthetic. Purity >95%. MW… | 50 mg | M-155 | More Info |
Mecamylamine hydrochloride | Mecamylamine blocks nAChRs with IC50s ~ 400 nM for α3/β4 and ~… | 10 mg | M-105 | More Info |
Mecamylamine hydrochloride | Mecamylamine blocks nAChRs with IC50s ~ 400 nM for α3/β4 and ~… | 100 mg | M-105 | More Info |
Mecamylamine hydrochloride | Mecamylamine blocks nAChRs with IC50s ~ 400 nM for α3/β4 and ~… | 25 mg | M-105 | More Info |
Mecamylamine hydrochloride | Mecamylamine blocks nAChRs with IC50s ~ 400 nM for α3/β4 and ~… | 5 mg | M-105 | More Info |
U.S.A. OFFICE
Toll free phone: 1800-618-1644 / 1800-791-3904
Toll free fax: 1888-454-7276 / 1800-791-3912