ALOMONE LABS Non-Antibody Products — page 31 of 36
Non-Antibody Products
Page 31 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| (S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 1 mg | A-267 | More Info |
| (S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 10 mg | A-267 | More Info |
| (S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 25 mg | A-267 | More Info |
| (S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 5 mg | A-267 | More Info |
| (S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 50 mg | A-267 | More Info |
| Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 0.1 mg | SPE-160 | More Info |
| Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 0.5 mg | SPE-160 | More Info |
| Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 1 mg | SPE-160 | More Info |
| Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 10 mg | SPE-160 | More Info |
| Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 5 mg | SPE-160 | More Info |
| (S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 25 mg | A-330 | More Info |
| (S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 5 mg | A-330 | More Info |
| (S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 10 mg | A-330 | More Info |
| SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 5 mg | S-370 | More Info |
| SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 5 x 1 mg | S-370 | More Info |
| SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 1 mg | S-370 | More Info |
| SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 0.5 mg | S-205 | More Info |
| SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 1 mg | S-205 | More Info |
| SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 2.5 mg | S-205 | More Info |
| SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 5 mg | S-205 | More Info |
| SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 10 mg | S-180 | More Info |
| SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 25 mg | S-180 | More Info |
| SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 50 mg | S-180 | More Info |
| SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 10 mg | S-160 | More Info |
| SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 100 mg | S-160 | More Info |
| SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 25 mg | S-160 | More Info |
| SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 5 mg | S-160 | More Info |
| SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 50 mg | S-160 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 1 mg | B-351 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 10 mg | B-351 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 100 mg | B-351 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 25 mg | B-351 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 5 mg | B-351 | More Info |
| (S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 50 mg | B-351 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.1 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.25 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.5 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 1 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 10 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 5 mg | STS-370 | More Info |
| Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 50 µg | STS-370 | More Info |
| (S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 100 mg | D-170 | More Info |
| (S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 25 mg | D-170 | More Info |
| (S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 250 mg | D-170 | More Info |
| (S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 50 mg | D-170 | More Info |
| SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 10 mg | S-145 | More Info |
| SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 25 mg | S-145 | More Info |
| SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 5 mg | S-145 | More Info |
| SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 50 mg | S-145 | More Info |
| SERCA Pump Inhibitor Explorer Kit | A Screening Package of SERCA Pump Inhibitors Economically Priced | 6 vials | EK-365 | More Info |
| Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 1 g | S-165 | More Info |
| Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 100 mg | S-165 | More Info |
| Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 250 mg | S-165 | More Info |
| Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 500 mg | S-165 | More Info |
| (S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 10 mg | F-205 | More Info |
| (S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 100 mg | F-205 | More Info |
| (S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 25 mg | F-205 | More Info |
| (S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 5 mg | F-205 | More Info |
| (S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 50 mg | F-205 | More Info |
| sFTX-3.3 | sFTX-3.3, a synthetic funnel web spider toxin1-2, is a polyamine amide ana… | 5 x 1 mg | F-130 | More Info |
| sFTX-3.3 | sFTX-3.3, a synthetic funnel web spider toxin1-2, is a polyamine amide ana… | 1 mg | F-130 | More Info |
| Shaker (KV1) Channel Blocker Explorer Kit | A Screening Package of Shaker (KV1) Channel Blockers Economically Priced | 27 vials | EK-107 | More Info |
| Shaker (KV)-Related Channel Blocker Explorer Kit | A Screening Package of Shaker (KV)-Related Channel Blockers Economically P… | 15 vials | EK-108 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 0.1 mg | STS-390 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 0.5 mg | STS-390 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 1 mg | STS-390 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 10 mg | STS-390 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 5 mg | STS-390 | More Info |
| ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 50 µg | STS-390 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.1 mg | STS-400 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.25 mg | STS-400 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.5 mg | STS-400 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 1 mg | STS-400 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 mg | STS-400 | More Info |
| ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 mg | STS-400 | More Info |
| Sitaxsentan | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 10 mg | S-186 | More Info |
| Sitaxsentan | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 25 mg | S-186 | More Info |
| Sitaxsentan | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 5 mg | S-186 | More Info |
| Sitaxsentan | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 50 mg | S-186 | More Info |
| Sitaxsentan sodium salt | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 10 mg | S-185 | More Info |
| Sitaxsentan sodium salt | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 100 mg | S-185 | More Info |
| Sitaxsentan sodium salt | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 25 mg | S-185 | More Info |
| Sitaxsentan sodium salt | Sitaxsentan is a potent and selective antagonist of ET-A Endothelin recept… | 50 mg | S-185 | More Info |
| SJM-3 | SJM-3 is a novel positive allosteric modulator of GABA(A) receptors at the… | 10 mg | S-215 | More Info |
| SJM-3 | SJM-3 is a novel positive allosteric modulator of GABA(A) receptors at the… | 25 mg | S-215 | More Info |
| SJM-3 | SJM-3 is a novel positive allosteric modulator of GABA(A) receptors at the… | 5 mg | S-215 | More Info |
| SJM-3 | SJM-3 is a novel positive allosteric modulator of GABA(A) receptors at the… | 50 mg | S-215 | More Info |
| SKA-121 | SKA-121 is a positive gating modulator of KCa3.1 channels (EC50 of 109 nM)… | 10 mg | S-245 | More Info |
| SKA-121 | SKA-121 is a positive gating modulator of KCa3.1 channels (EC50 of 109 nM)… | 25 mg | S-245 | More Info |
| SKA-121 | SKA-121 is a positive gating modulator of KCa3.1 channels (EC50 of 109 nM)… | 5 mg | S-245 | More Info |
| SKA-121 | SKA-121 is a positive gating modulator of KCa3.1 channels (EC50 of 109 nM)… | 50 mg | S-245 | More Info |
| SKA-31 | SKA-31 is an activator of KCa3.1 and KCa2 channels (EC50 values are 260, 2… | 10 mg | S-120 | More Info |
| SKA-31 | SKA-31 is an activator of KCa3.1 and KCa2 channels (EC50 values are 260, 2… | 25 mg | S-120 | More Info |
| SKA-31 | SKA-31 is an activator of KCa3.1 and KCa2 channels (EC50 values are 260, 2… | 5 mg | S-120 | More Info |
| SKA-31 | SKA-31 is an activator of KCa3.1 and KCa2 channels (EC50 values are 260, 2… | 50 mg | S-120 | More Info |
| SKF 96365 hydrochloride | SKF 96365 is an Inhibitor of TRPC channels and inhibitor of T-type calcium… | 10 mg | S-175 | More Info |
| SKF 96365 hydrochloride | SKF 96365 is an Inhibitor of TRPC channels and inhibitor of T-type calcium… | 25 mg | S-175 | More Info |
| SKF 96365 hydrochloride | SKF 96365 is an Inhibitor of TRPC channels and inhibitor of T-type calcium… | 5 mg | S-175 | More Info |
| SKF 96365 hydrochloride | SKF 96365 is an Inhibitor of TRPC channels and inhibitor of T-type calcium… | 50 mg | S-175 | More Info |
| SLIGKV-NH2 | SLIGKV-NH2 is a selective agonist of the Protease-activated receptor-2 (PA… | 1 mg | GPS-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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