ALOMONE LABS Non-Antibody Products — page 33 of 36
Non-Antibody Products
Page 33 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 25 g | T-130 | More Info |
| Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 5 g | T-130 | More Info |
| tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 1 g | T-220 | More Info |
| tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 250 mg | T-220 | More Info |
| tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 5 g | T-220 | More Info |
| TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 10 mg | T-200 | More Info |
| TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 25 mg | T-200 | More Info |
| TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 5 mg | T-200 | More Info |
| TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 50 mg | T-200 | More Info |
| TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 10 mg | T-190 | More Info |
| TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 100 mg | T-190 | More Info |
| TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 25 mg | T-190 | More Info |
| TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 5 mg | T-190 | More Info |
| TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 50 mg | T-190 | More Info |
| TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 10 mg | T-215 | More Info |
| TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 25 mg | T-215 | More Info |
| TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 5 mg | T-215 | More Info |
| TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 50 mg | T-215 | More Info |
| Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 1 g | T-170 | More Info |
| Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 100 mg | T-170 | More Info |
| Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 250 mg | T-170 | More Info |
| Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 50 mg | T-170 | More Info |
| Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 500 mg | T-170 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 0.1 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 0.25 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 0.5 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 1 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 10 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 5 mg | STT-250 | More Info |
| Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 5 x 0.1 mg | STT-250 | More Info |
| Tertiapin-LQ | Tertiapin-LQ is a selective blocker of Kir1.1 channels. Synthetic peptide.… | 1 mg | STT-220 | More Info |
| Tertiapin-LQ | Tertiapin-LQ is a selective blocker of Kir1.1 channels. Synthetic peptide.… | 10 mg | STT-220 | More Info |
| Tertiapin-LQ | Tertiapin-LQ is a selective blocker of Kir1.1 channels. Synthetic peptide.… | 5 mg | STT-220 | More Info |
| Tertiapin-LQ | Tertiapin-LQ is a selective blocker of Kir1.1 channels. Synthetic peptide.… | 0.5 mg | STT-220 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 0.1 mg | STT-170 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 0.25 mg | STT-170 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 0.5 mg | STT-170 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 1 mg | STT-170 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 10 mg | STT-170 | More Info |
| Tertiapin-Q | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 5 mg | STT-170 | More Info |
| Tertiapin-Q-ATTO Fluor-488 | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 5 x 5 µg | STT-170-AG | More Info |
| Tertiapin-Q-ATTO Fluor-488 | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 5 µg | STT-170-AG | More Info |
| Tertiapin-Q-ATTO Fluor-633 | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 5 x 5 µg | STT-170-FR | More Info |
| Tertiapin-Q-ATTO Fluor-633 | Tertiapin-Q blocks a range of inward rectifier K+ channels (Kir), in parti… | 5 µg | STT-170-FR | More Info |
| Tertiapin-RQ | Tertiapin-RQ blocks a range of inward rectifier K+ channels (Kir), in part… | 0.1 mg | STT-180 | More Info |
| Tertiapin-RQ | Tertiapin-RQ blocks a range of inward rectifier K+ channels (Kir), in part… | 0.5 mg | STT-180 | More Info |
| Tertiapin-RQ | Tertiapin-RQ blocks a range of inward rectifier K+ channels (Kir), in part… | 1 mg | STT-180 | More Info |
| Tertiapin-RQ | Tertiapin-RQ blocks a range of inward rectifier K+ channels (Kir), in part… | 5 mg | STT-180 | More Info |
| Tetanus Toxin | Tetanus Toxin inhibits neurotransmitter release by cleaving synaptobrevin-… | 5 x 10 µg | T-150 | More Info |
| Tetanus Toxin | Tetanus Toxin inhibits neurotransmitter release by cleaving synaptobrevin-… | 10 µg | T-150 | More Info |
| Tetrodotoxin citrate | Tetrodotoxin is a potent and selective blocker of a subclass of NaV channe… | 1 mg | T-550 | More Info |
| Tetrodotoxin citrate | Tetrodotoxin is a potent and selective blocker of a subclass of NaV channe… | 5 x 1 mg | T-550 | More Info |
| Tetrodotoxin citrate | Tetrodotoxin is a potent and selective blocker of a subclass of NaV channe… | 50 µg | T-550 | More Info |
| Tetrodotoxin citrate free | Tetrodotoxin is a potent and selective blocker of a subclass of NaV channe… | 5 x 1 mg | T-500 | More Info |
| Tetrodotoxin citrate free | Tetrodotoxin is a potent and selective blocker of a subclass of NaV channe… | 1 mg | T-500 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 0.1 mg | STT-050 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 0.25 mg | STT-050 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 0.5 mg | STT-050 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 1 mg | STT-050 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 10 mg | STT-050 | More Info |
| Tf2 Toxin | Tf2 Toxin is a NaV1.3 and NaV1.9 channel opener1,2. Synthetic peptide. Pur… | 5 mg | STT-050 | More Info |
| Thapsigargin | Thapsigargin is a highly potent inhibitor of the sarco-endoplasmic reticul… | 0.65 mg | T-650 | More Info |
| Thapsigargin | Thapsigargin is a highly potent inhibitor of the sarco-endoplasmic reticul… | 1 mg | T-650 | More Info |
| Thapsigargin | Thapsigargin is a highly potent inhibitor of the sarco-endoplasmic reticul… | 10 mg | T-650 | More Info |
| Thapsigargin | Thapsigargin is a highly potent inhibitor of the sarco-endoplasmic reticul… | 5 mg | T-650 | More Info |
| Thapsigargin Epoxide | Thapsigargin is an extremely tight-binding inhibitor of intracellular Ca2+… | 5 x 5 mg | T-670 | More Info |
| Thapsigargin Epoxide | Thapsigargin is an extremely tight-binding inhibitor of intracellular Ca2+… | 50 µg | T-670 | More Info |
| Thapsigargin Epoxide | Thapsigargin is an extremely tight-binding inhibitor of intracellular Ca2+… | 5 mg | T-670 | More Info |
| Tityustoxin-Kα | Tityustoxin-Kα blocks cloned KV1.2 with high potency1. Synthetic pep… | 0.1 mg | STT-360 | More Info |
| Tityustoxin-Kα | Tityustoxin-Kα blocks cloned KV1.2 with high potency1. Synthetic pep… | 0.5 mg | STT-360 | More Info |
| Tityustoxin-Kα | Tityustoxin-Kα blocks cloned KV1.2 with high potency1. Synthetic pep… | 1 mg | STT-360 | More Info |
| Tityustoxin-Kα | Tityustoxin-Kα blocks cloned KV1.2 with high potency1. Synthetic pep… | 10 mg | STT-360 | More Info |
| Tityustoxin-Kα | Tityustoxin-Kα blocks cloned KV1.2 with high potency1. Synthetic pep… | 5 mg | STT-360 | More Info |
| Tityustoxin-Kα-ATTO Fluor-594 | Tityustoxin-Kα blocks cloned KV1.2 with high potency1,2.Using Alomon… | 5 x 5 µg | STT-360-AR | More Info |
| Tityustoxin-Kα-ATTO Fluor-594 | Tityustoxin-Kα blocks cloned KV1.2 with high potency1,2.Using Alomon… | 5 µg | STT-360-AR | More Info |
| TMB-8 hydrochloride | SERCA pump inhibitor. Purity ≥87%. MW: 432 | 5 mg | T-245 | More Info |
| Tolperisone hydrochloride | Tolperisone is a centrally acting muscle relaxant1 used for the treatment… | 100 mg | T-115 | More Info |
| Tolperisone hydrochloride | Tolperisone is a centrally acting muscle relaxant1 used for the treatment… | 25 mg | T-115 | More Info |
| Tolperisone hydrochloride | Tolperisone is a centrally acting muscle relaxant1 used for the treatment… | 250 mg | T-115 | More Info |
| Tolperisone hydrochloride | Tolperisone is a centrally acting muscle relaxant1 used for the treatment… | 50 mg | T-115 | More Info |
| Topotecan | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.985. MW: 4… | 10 mg | T-161 | More Info |
| Topotecan | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.985. MW: 4… | 25 mg | T-161 | More Info |
| Topotecan | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.985. MW: 4… | 5 mg | T-161 | More Info |
| Topotecan | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.985. MW: 4… | 50 mg | T-161 | More Info |
| Topotecan hydrochloride | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.99. MW: 45… | 10 mg | T-160 | More Info |
| Topotecan hydrochloride | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.99. MW: 45… | 25 mg | T-160 | More Info |
| Topotecan hydrochloride | Topotecan is a 5-HT3A receptor antagonist1. Synthetic. Purity 0.99. MW: 45… | 50 mg | T-160 | More Info |
| Tracazolate hydrochloride | Tracazolate is an allosteric modulator of GABA(A) receptors, that was show… | 10 mg | T-230 | More Info |
| Tracazolate hydrochloride | Tracazolate is an allosteric modulator of GABA(A) receptors, that was show… | 25 mg | T-230 | More Info |
| Tracazolate hydrochloride | Tracazolate is an allosteric modulator of GABA(A) receptors, that was show… | 5 mg | T-230 | More Info |
| Tracazolate hydrochloride | Tracazolate is an allosteric modulator of GABA(A) receptors, that was show… | 50 mg | T-230 | More Info |
| TRAM 34 | TRAM 34 is a potent and selective KCa3.1 (SK4, intermediate conductance Ca… | 10 mg | T-105 | More Info |
| TRAM 34 | TRAM 34 is a potent and selective KCa3.1 (SK4, intermediate conductance Ca… | 25 mg | T-105 | More Info |
| TRAM 34 | TRAM 34 is a potent and selective KCa3.1 (SK4, intermediate conductance Ca… | 5 mg | T-105 | More Info |
| TRAM 34 | TRAM 34 is a potent and selective KCa3.1 (SK4, intermediate conductance Ca… | 50 mg | T-105 | More Info |
| trans-ACBD | trans-ACBD is an NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 159… | 10 mg | A-280 | More Info |
| trans-ACBD | trans-ACBD is an NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 159… | 25 mg | A-280 | More Info |
| trans-ACBD | trans-ACBD is an NMDA receptor agonist1,2. Synthetic. Purity >95%. MW: 159… | 5 mg | A-280 | More Info |
| Triacsin C | Triacsin C nearly completely inhibits de novo synthesis of triacylglycerol… | 1 mg | T-750 | More Info |
| Triacsin C | Triacsin C nearly completely inhibits de novo synthesis of triacylglycerol… | 5 x 0.2 mg | T-750 | 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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