ALOMONE LABS Non-Antibody Products — page 32 of 36
Non-Antibody Products
Page 32 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| SLIGKV-NH2 | SLIGKV-NH2 is a selective agonist of the Protease-activated receptor-2 (PA… | 100 mg | GPS-100 | More Info |
| SLIGKV-NH2 | SLIGKV-NH2 is a selective agonist of the Protease-activated receptor-2 (PA… | 25 mg | GPS-100 | More Info |
| SLIGKV-NH2 | SLIGKV-NH2 is a selective agonist of the Protease-activated receptor-2 (PA… | 5 mg | GPS-100 | More Info |
| Slotoxin | Slotoxin inhibits the Maxi K+ (BKCa or mSlo, KCNMA1, KCa1.1) channels1. Sl… | 0.1 mg | STS-410 | More Info |
| Slotoxin | Slotoxin inhibits the Maxi K+ (BKCa or mSlo, KCNMA1, KCa1.1) channels1. Sl… | 0.5 mg | STS-410 | More Info |
| Slotoxin | Slotoxin inhibits the Maxi K+ (BKCa or mSlo, KCNMA1, KCa1.1) channels1. Sl… | 1 mg | STS-410 | More Info |
| Slotoxin | Slotoxin inhibits the Maxi K+ (BKCa or mSlo, KCNMA1, KCa1.1) channels1. Sl… | 10 mg | STS-410 | More Info |
| Slotoxin | Slotoxin inhibits the Maxi K+ (BKCa or mSlo, KCNMA1, KCa1.1) channels1. Sl… | 5 mg | STS-410 | More Info |
| SNAP 37889 | SNAP 37889 is a potent GalR3 galanin receptor antagonist, highly selective… | 10 mg | S-210 | More Info |
| SNAP 37889 | SNAP 37889 is a potent GalR3 galanin receptor antagonist, highly selective… | 100 mg | S-210 | More Info |
| SNAP 37889 | SNAP 37889 is a potent GalR3 galanin receptor antagonist, highly selective… | 25 mg | S-210 | More Info |
| SNAP 37889 | SNAP 37889 is a potent GalR3 galanin receptor antagonist, highly selective… | 50 mg | S-210 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 0.1 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 0.25 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 0.5 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 1 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 2.5 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 25 µg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 5 mg | RTS-500 | More Info |
| SNX-482 | SNX-482 blocks R-type (CaV2.3) and P / Q-type (CaV2.1) voltage-gated Ca2+… | 50 µg | RTS-500 | More Info |
| Spinoxin | Spinoxin is a potent blocker of KV1.2 and KV1.3 channels1. Synthetic pepti… | 0.1 mg | STS-500 | More Info |
| Spinoxin | Spinoxin is a potent blocker of KV1.2 and KV1.3 channels1. Synthetic pepti… | 0.5 mg | STS-500 | More Info |
| Spinoxin | Spinoxin is a potent blocker of KV1.2 and KV1.3 channels1. Synthetic pepti… | 1 mg | STS-500 | More Info |
| Spinoxin | Spinoxin is a potent blocker of KV1.2 and KV1.3 channels1. Synthetic pepti… | 5 mg | STS-500 | More Info |
| Spinoxin | Spinoxin is a potent blocker of KV1.2 and KV1.3 channels1. Synthetic pepti… | 50 µg | STS-500 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 0.5 mg | STS-800 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 1 mg | STS-800 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 10 mg | STS-800 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 5 mg | STS-800 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 50 µg | STS-800 | More Info |
| SpTx-1 | SpTx-1 inhibits hKATP channels with a Kd of 15 nM by blocking the hKir6.2… | 0.1 mg | STS-800 | More Info |
| SR 48527 | SR 48527, an analog of SR 48692, is a potent and selective antagonist of N… | 10 mg | S-225 | More Info |
| SR 48527 | SR 48527, an analog of SR 48692, is a potent and selective antagonist of N… | 25 mg | S-225 | More Info |
| SR 48527 | SR 48527, an analog of SR 48692, is a potent and selective antagonist of N… | 5 mg | S-225 | More Info |
| SR 48527 | SR 48527, an analog of SR 48692, is a potent and selective antagonist of N… | 50 mg | S-225 | More Info |
| SR 48692 | SR 48692 is a potent and selective non-peptide antagonist of NTS1 receptor… | 10 mg | S-265 | More Info |
| SR 48692 | SR 48692 is a potent and selective non-peptide antagonist of NTS1 receptor… | 25 mg | S-265 | More Info |
| SR 48692 | SR 48692 is a potent and selective non-peptide antagonist of NTS1 receptor… | 5 mg | S-265 | More Info |
| SR 48692 | SR 48692 is a potent and selective non-peptide antagonist of NTS1 receptor… | 50 mg | S-265 | More Info |
| SR 57227A | SR 57227A is a high affinity, selective 5-HT3 receptor agonist, active in… | 10 mg | S-155 | More Info |
| SR 57227A | SR 57227A is a high affinity, selective 5-HT3 receptor agonist, active in… | 25 mg | S-155 | More Info |
| SR 57227A | SR 57227A is a high affinity, selective 5-HT3 receptor agonist, active in… | 5 mg | S-155 | More Info |
| SR 57227A | SR 57227A is a high affinity, selective 5-HT3 receptor agonist, active in… | 50 mg | S-155 | More Info |
| SR 33805 oxalate | SR 33805, a fantofarone derivative, is a potent Ca2+ channel antagonist1.… | 10 mg | S-105 | More Info |
| SR 33805 oxalate | SR 33805, a fantofarone derivative, is a potent Ca2+ channel antagonist1.… | 25 mg | S-105 | More Info |
| SR 33805 oxalate | SR 33805, a fantofarone derivative, is a potent Ca2+ channel antagonist1.… | 5 mg | S-105 | More Info |
| SR 33805 oxalate | SR 33805, a fantofarone derivative, is a potent Ca2+ channel antagonist1.… | 50 mg | S-105 | More Info |
| SsdTx3 | SsdTx3 inhibits hKATP channels with a Kd of <300 nM by blocking the hKi… | 0.1 mg | STS-670 | More Info |
| SsdTx3 | SsdTx3 inhibits hKATP channels with a Kd of <300 nM by blocking the hKi… | 0.5 mg | STS-670 | More Info |
| SsdTx3 | SsdTx3 inhibits hKATP channels with a Kd of <300 nM by blocking the hKi… | 1 mg | STS-670 | More Info |
| SsdTx3 | SsdTx3 inhibits hKATP channels with a Kd of <300 nM by blocking the hKi… | 5 mg | STS-670 | More Info |
| SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 0.25 mg | STS-700 | More Info |
| SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 0.5 mg | STS-700 | More Info |
| SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 1 mg | STS-700 | More Info |
| SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 10 mg | STS-700 | More Info |
| SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 5 mg | STS-700 | More Info |
| Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 0.1 mg | S-350 | More Info |
| Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 0.47 mg | S-350 | More Info |
| Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 1 mg | S-350 | More Info |
| Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 5 x 50 µg | S-350 | More Info |
| Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 50 µg | S-350 | More Info |
| Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 µg | STS-400-AR | More Info |
| Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 x 5 µg | STS-400-AR | More Info |
| Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 x 5 µg | STS-400-AR | More Info |
| Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 µg | STS-400-B | More Info |
| Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 x 5 µg | STS-400-B | More Info |
| Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 x 5 µg | STS-400-B | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.1 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.25 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.5 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 1 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 10 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 5 mg | STS-350 | More Info |
| Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 50 µg | STS-350 | More Info |
| Taipoxin | Taipoxin gradually and completely stops induced and spontaneous release of… | 5 x 0.5 mg | T-460 | More Info |
| Taipoxin | Taipoxin gradually and completely stops induced and spontaneous release of… | 0.5 mg | T-460 | More Info |
| TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 10 mg | SPE-320 | More Info |
| TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 25 mg | SPE-320 | More Info |
| TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 5 mg | SPE-320 | More Info |
| Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 10 mg | T-185 | More Info |
| Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 25 mg | T-185 | More Info |
| Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 5 mg | T-185 | More Info |
| Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 50 mg | T-185 | More Info |
| Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 10 mg | B-140 | More Info |
| Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 25 mg | B-140 | More Info |
| Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 5 mg | B-140 | More Info |
| Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 50 mg | B-140 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.1 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.25 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.5 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 1 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 10 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 5 mg | STT-400 | More Info |
| Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 50 µg | STT-400 | More Info |
| Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 10 mg | T-165 | More Info |
| Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 25 mg | T-165 | More Info |
| Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 5 mg | T-165 | More Info |
| Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 50 mg | T-165 | More Info |
| Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 10 g | T-130 | More Info |
| Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 100 g | T-130 | 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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