ALOMONE LABS Non-Antibody Products — page 30 of 71
Non-Antibody Products
Page 30 of 71
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 0.1 mg | STH-105 | More Info |
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 0.25 mg | STH-105 | More Info |
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 0.5 mg | STH-105 | More Info |
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 1 mg | STH-105 | More Info |
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 10 mg | STH-105 | More Info |
| Huwentoxin-XVI | Huwentoxin-XVI is a potent and reversible N-type Ca2+ channel blocker1. Sy… | 5 mg | STH-105 | More Info |
| 5-Hydroxyindole | 5-Hydroxyindole is a 5-HT3 receptor allosteric modulator which slows the d… | 1 g | H-115 | More Info |
| 5-Hydroxyindole | 5-Hydroxyindole is a 5-HT3 receptor allosteric modulator which slows the d… | 250 mg | H-115 | More Info |
| Iberiotoxin | Iberiotoxin is a potent selective blocker of the high conductance Ca2+-act… | 0.1 mg | STI-400 | More Info |
| Iberiotoxin | Iberiotoxin is a potent selective blocker of the high conductance Ca2+-act… | 0.5 mg | STI-400 | More Info |
| Iberiotoxin | Iberiotoxin is a potent selective blocker of the high conductance Ca2+-act… | 1 mg | STI-400 | More Info |
| Iberiotoxin | Iberiotoxin is a potent selective blocker of the high conductance Ca2+-act… | 10 mg | STI-400 | More Info |
| Iberiotoxin | Iberiotoxin is a potent selective blocker of the high conductance Ca2+-act… | 5 mg | STI-400 | More Info |
| ICA 121431 | ICA 121431 blocks NaV channels with IC50 values of 13 and 23 nM for NaV1.3… | 10 mg | I-170 | More Info |
| ICA 121431 | ICA 121431 blocks NaV channels with IC50 values of 13 and 23 nM for NaV1.3… | 25 mg | I-170 | More Info |
| ICA 121431 | ICA 121431 blocks NaV channels with IC50 values of 13 and 23 nM for NaV1.3… | 5 mg | I-170 | More Info |
| ICA 121431 | ICA 121431 blocks NaV channels with IC50 values of 13 and 23 nM for NaV1.3… | 50 mg | I-170 | More Info |
| ICA-110381 | ICA-110381 is a KCNQ channel opener with anti-convulsive properties1. Synt… | 10 mg | I-160 | More Info |
| ICA-110381 | ICA-110381 is a KCNQ channel opener with anti-convulsive properties1. Synt… | 25 mg | I-160 | More Info |
| ICA-110381 | ICA-110381 is a KCNQ channel opener with anti-convulsive properties1. Synt… | 5 mg | I-160 | More Info |
| ICA-110381 | ICA-110381 is a KCNQ channel opener with anti-convulsive properties1. Synt… | 50 mg | I-160 | More Info |
| ICA-27243 | ICA-27243 is a potent and selective KCNQ channel modulator (enhancer)1 wit… | 10 mg | I-130 | More Info |
| ICA-27243 | ICA-27243 is a potent and selective KCNQ channel modulator (enhancer)1 wit… | 25 mg | I-130 | More Info |
| ICA-27243 | ICA-27243 is a potent and selective KCNQ channel modulator (enhancer)1 wit… | 5 mg | I-130 | More Info |
| ICA-27243 | ICA-27243 is a potent and selective KCNQ channel modulator (enhancer)1 wit… | 50 mg | I-130 | More Info |
| Icilin | Icilin is a potent TRPM8 channel activator (EC50 = 0.2 µM)1. Synthet… | 10 mg | I-145 | More Info |
| Icilin | Icilin is a potent TRPM8 channel activator (EC50 = 0.2 µM)1. Synthet… | 100 mg | I-145 | More Info |
| Icilin | Icilin is a potent TRPM8 channel activator (EC50 = 0.2 µM)1. Synthet… | 25 mg | I-145 | More Info |
| Icilin | Icilin is a potent TRPM8 channel activator (EC50 = 0.2 µM)1. Synthet… | 5 mg | I-145 | More Info |
| Icilin | Icilin is a potent TRPM8 channel activator (EC50 = 0.2 µM)1. Synthet… | 50 mg | I-145 | More Info |
| IDRA 21 | IDRA 21 is a selective AMPA receptor agonist1. Synthetic. Purity >99%. MW:… | 25 mg | I-140 | More Info |
| IDRA 21 | IDRA 21 is a selective AMPA receptor agonist1. Synthetic. Purity >99%. MW:… | 5 mg | I-140 | More Info |
| IDRA 21 | IDRA 21 is a selective AMPA receptor agonist1. Synthetic. Purity >99%. MW:… | 50 mg | I-140 | More Info |
| IDRA 21 | IDRA 21 is a selective AMPA receptor agonist1. Synthetic. Purity >99%. MW:… | 10 mg | I-140 | More Info |
| IEM-1921 | IEM-1921 is a selective NMDA receptor blocker and is a potent anticonvulsa… | 10 mg | I-180 | More Info |
| IEM-1921 | IEM-1921 is a selective NMDA receptor blocker and is a potent anticonvulsa… | 25 mg | I-180 | More Info |
| IEM-1921 | IEM-1921 is a selective NMDA receptor blocker and is a potent anticonvulsa… | 5 mg | I-180 | More Info |
| IEM-1921 | IEM-1921 is a selective NMDA receptor blocker and is a potent anticonvulsa… | 50 mg | I-180 | More Info |
| Ifenprodil (+)-tartrate salt (hemitartrate salt) | Ifenprodil inhibits NMDA receptors with the following IC50s: 0.15 µM… | 10 mg | I-105 | More Info |
| Ifenprodil (+)-tartrate salt (hemitartrate salt) | Ifenprodil inhibits NMDA receptors with the following IC50s: 0.15 µM… | 25 mg | I-105 | More Info |
| Ifenprodil (+)-tartrate salt (hemitartrate salt) | Ifenprodil inhibits NMDA receptors with the following IC50s: 0.15 µM… | 5 mg | I-105 | More Info |
| Ifenprodil (+)-tartrate salt (hemitartrate salt) | Ifenprodil inhibits NMDA receptors with the following IC50s: 0.15 µM… | 50 mg | I-105 | More Info |
| Imperatoxin A | Imperatoxin A is a strong agonist of ryanodine receptor channels (RyR)1. I… | 0.1 mg | STI-333 | More Info |
| Imperatoxin A | Imperatoxin A is a strong agonist of ryanodine receptor channels (RyR)1. I… | 0.5 mg | STI-333 | More Info |
| Imperatoxin A | Imperatoxin A is a strong agonist of ryanodine receptor channels (RyR)1. I… | 1 mg | STI-333 | More Info |
| Imperatoxin A | Imperatoxin A is a strong agonist of ryanodine receptor channels (RyR)1. I… | 10 mg | STI-333 | More Info |
| Imperatoxin A | Imperatoxin A is a strong agonist of ryanodine receptor channels (RyR)1. I… | 5 mg | STI-333 | More Info |
| Indisetron dihydrochloride | Indesitron is a specifiic 5-HT3 antagonist, with an IC50 of 23 nM for inhi… | 10 mg | I-175 | More Info |
| Indisetron dihydrochloride | Indesitron is a specifiic 5-HT3 antagonist, with an IC50 of 23 nM for inhi… | 25 mg | I-175 | More Info |
| Indisetron dihydrochloride | Indesitron is a specifiic 5-HT3 antagonist, with an IC50 of 23 nM for inhi… | 5 mg | I-175 | 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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