ALOMONE LABS Non-Antibody Products — page 61 of 71
Non-Antibody Products
Page 61 of 71
| 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 |
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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