ALOMONE LABS Non-Antibody Products — page 66 of 71

Non-Antibody Products
Page 66 of 71
  • Records 3,251 - 3,300 of 3,505
Name Description Size Catalog #
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
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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