ALOMONE LABS Non-Antibody Products — page 19 of 36
Non-Antibody Products
Page 19 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 50 µg | STM-100 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 0.1 mg | STM-400 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 0.5 mg | STM-400 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 1 mg | STM-400 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 10 mg | STM-400 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 5 mg | STM-400 | More Info |
| Mambalgin-2 | Mambalgin-2 is a blocker of ASIC1 channels1. Synthetic peptide. Purity >98… | 50 µg | STM-400 | More Info |
| Mambalgin-3 | A blocker of ASIC1-containing channels1,2. Synthetic peptide. Purity >98%… | 0.1 mg | STM-500 | More Info |
| Mambalgin-3 | A blocker of ASIC1-containing channels1,2. Synthetic peptide. Purity >98%… | 0.5 mg | STM-500 | More Info |
| Mambalgin-3 | A blocker of ASIC1-containing channels1,2. Synthetic peptide. Purity >98%… | 1 mg | STM-500 | More Info |
| Mambalgin-3 | A blocker of ASIC1-containing channels1,2. Synthetic peptide. Purity >98%… | 5 mg | STM-500 | More Info |
| Mambalgin-3 | A blocker of ASIC1-containing channels1,2. Synthetic peptide. Purity >98%… | 50 µg | STM-500 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 0.1 mg | STM-325 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 0.25 mg | STM-325 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 0.5 mg | STM-325 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 1 mg | STM-325 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 10 mg | STM-325 | More Info |
| Margatoxin | Margatoxin is a blocker of KV1.3 and KV1.6 channels. Synthetic peptide. Pu… | 5 mg | STM-325 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 0.1 mg | RTM-100 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 0.25 mg | RTM-100 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 0.5 mg | RTM-100 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 1 mg | RTM-100 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 10 mg | RTM-100 | More Info |
| Maurocalcine | Maurocalcine is an agonist of Ryanodine receptor channel (RyR) types 1' 2… | 5 mg | RTM-100 | More Info |
| Maurotoxin | Maurotoxin activity was extensively assayed on a large array of K+ channel… | 0.1 mg | STM-340 | More Info |
| 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 |
| Mecamylamine hydrochloride | Mecamylamine blocks nAChRs with IC50s ~ 400 nM for α3/β4 and ~… | 50 mg | M-105 | More Info |
| Meclofenamic acid | Meclofenamic acid is a KCNQ2 / KCNQ3 channel opener, non-steroidal anti-in… | 10 mg | M-210 | More Info |
| Meclofenamic acid | Meclofenamic acid is a KCNQ2 / KCNQ3 channel opener, non-steroidal anti-in… | 25 mg | M-210 | More Info |
| Meclofenamic acid | Meclofenamic acid is a KCNQ2 / KCNQ3 channel opener, non-steroidal anti-in… | 5 mg | M-210 | More Info |
| Meclofenamic acid | Meclofenamic acid is a KCNQ2 / KCNQ3 channel opener, non-steroidal anti-in… | 50 mg | M-210 | More Info |
| Memantine hydrochloride | Memantine is an NMDA receptor antagonist. IC50 = 0.8 µM (NR2A), 0.5… | 100 mg | M-145 | More Info |
| Memantine hydrochloride | Memantine is an NMDA receptor antagonist. IC50 = 0.8 µM (NR2A), 0.5… | 250 mg | M-145 | More Info |
| Memantine hydrochloride | Memantine is an NMDA receptor antagonist. IC50 = 0.8 µM (NR2A), 0.5… | 50 mg | M-145 | More Info |
| Memantine hydrochloride | Memantine is an NMDA receptor antagonist. IC50 = 0.8 µM (NR2A), 0.5… | 500 mg | M-145 | More Info |
| 2'MeO6MF | 2'MeO6MF is a GABAA receptor modulator, shown to potentiate the response t… | 10 mg | M-245 | More Info |
| 2'MeO6MF | 2'MeO6MF is a GABAA receptor modulator, shown to potentiate the response t… | 25 mg | M-245 | More Info |
| 2'MeO6MF | 2'MeO6MF is a GABAA receptor modulator, shown to potentiate the response t… | 5 mg | M-245 | More Info |
| 2'MeO6MF | 2'MeO6MF is a GABAA receptor modulator, shown to potentiate the response t… | 50 mg | M-245 | More Info |
| Mepivacaine hydrochloride | Mepivacaine hydrochloride is a local anesthetic1 which reversibly blocks v… | 1 g | M-110 | More Info |
| Mepivacaine hydrochloride | Mepivacaine hydrochloride is a local anesthetic1 which reversibly blocks v… | 250 mg | M-110 | More Info |
| Mepivacaine hydrochloride | Mepivacaine hydrochloride is a local anesthetic1 which reversibly blocks v… | 500 mg | M-110 | More Info |
| 2-Methyl-5-hydroxytryptamine hydrochloride | Methyl serotonin is a 5-HT3 agonist (Ki = 1200 nM) and potent 5-HT6 ligand… | 10 mg | M-170 | More Info |
| 2-Methyl-5-hydroxytryptamine hydrochloride | Methyl serotonin is a 5-HT3 agonist (Ki = 1200 nM) and potent 5-HT6 ligand… | 25 mg | M-170 | More Info |
| 2-Methyl-5-hydroxytryptamine hydrochloride | Methyl serotonin is a 5-HT3 agonist (Ki = 1200 nM) and potent 5-HT6 ligand… | 5 mg | M-170 | More Info |
| 2-Methyl-5-hydroxytryptamine hydrochloride | Methyl serotonin is a 5-HT3 agonist (Ki = 1200 nM) and potent 5-HT6 ligand… | 50 mg | M-170 | More Info |
| Mexiletine hydrochloride | Mexiletine is an orally effective antiarrhythmic drug of the IB class1-4 w… | 1 g | M-115 | More Info |
| Mexiletine hydrochloride | Mexiletine is an orally effective antiarrhythmic drug of the IB class1-4 w… | 100 g | M-115 | More Info |
| Mexiletine hydrochloride | Mexiletine is an orally effective antiarrhythmic drug of the IB class1-4 w… | 25 g | M-115 | More Info |
| Mexiletine hydrochloride | Mexiletine is an orally effective antiarrhythmic drug of the IB class1-4 w… | 50 g | M-115 | More Info |
| mGluR1 Antagonist Explorer Kit | A Screening Package of mGluR1 Antagonists Economically Priced | 13 vials | EK-250 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 0.1 mg | STH-102 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 0.5 mg | STH-102 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 1 mg | STH-102 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 10 mg | STH-102 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 5 mg | STH-102 | More Info |
| m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 50 µg | STH-102 | More Info |
| mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 0.1 mg | STH-101 | More Info |
| mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 0.5 mg | STH-101 | More Info |
| mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 5 x 50 µg | STH-101 | More Info |
| mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 50 µg | STH-101 | More Info |
| Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 1 mg | M-150 | More Info |
| Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 10 mg | M-150 | More Info |
| Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 25 mg | M-150 | More Info |
| Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 5 mg | M-150 | More Info |
| Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 50 mg | M-150 | More Info |
| Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 1 g | M-206 | More Info |
| Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 10 g | M-206 | More Info |
| Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 25 g | M-206 | More Info |
| Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 5 g | M-206 | More Info |
| Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 100 mg | M-130 | More Info |
| Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 25 mg | M-130 | More Info |
| Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 50 mg | M-130 | More Info |
| MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.1 mg | M-100 | More Info |
| MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.25 mg | M-100 | More Info |
| MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.5 mg | M-100 | More Info |
ALOMONE LABS
ALOMONE LABS
Jerusalem BioPark (JBP), Hadassah Ein Kerem
PO Box 4287
Jerusalem, 9104201 ISRAEL
P: +972-2-587-2202
F: +972-2-587-1101
info@alomone.com
http://www.alomone.com
U.S.A. OFFICE
Toll free phone: 1800-618-1644 / 1800-791-3904
Toll free fax: 1888-454-7276 / 1800-791-3912
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