ALOMONE LABS Non-Antibody Products — page 54 of 71
Non-Antibody Products
Page 54 of 71
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| Puromycin | Puromycin is an antibiotic known to inhibit protein synthesis1, as well as… | 50 mg | P-540 | More Info |
| Puromycin | Puromycin is an antibiotic known to inhibit protein synthesis1, as well as… | 500 mg | P-540 | More Info |
| P2X7 Receptor Antagonist Explorer Kit | A Screening Package of P2X7 Receptor Antagonists Economically Priced | 13 vials | EK-410 | More Info |
| P2X7 Receptor Basic Research Pack | All You Need for P2X7 Receptor Research | 7 vials | ESB-710 | More Info |
| P2X7 Receptor Deluxe Research Pack | All You Need for P2X7 Receptor Research | 15 vials | ESD-710 | More Info |
| P2X7 Receptor Premium Research Pack | All You Need for P2X7 Receptor Research | 10 vials | ESP-710 | More Info |
| Pyrrolopyrimidine 48 | Pyrrolopyrimidine 48 is a blocker of NaV1.7 channel with an IC50 value of… | 10 mg | P-275 | More Info |
| Pyrrolopyrimidine 48 | Pyrrolopyrimidine 48 is a blocker of NaV1.7 channel with an IC50 value of… | 25 mg | P-275 | More Info |
| Pyrrolopyrimidine 48 | Pyrrolopyrimidine 48 is a blocker of NaV1.7 channel with an IC50 value of… | 5 mg | P-275 | More Info |
| Pyrrolopyrimidine 48 | Pyrrolopyrimidine 48 is a blocker of NaV1.7 channel with an IC50 value of… | 50 mg | P-275 | More Info |
| QNZ 46 | QNZ-46 is a potent, noncompetitive NMDA receptor antagonist, exhibiting si… | 10 mg | Q-270 | More Info |
| QNZ 46 | QNZ-46 is a potent, noncompetitive NMDA receptor antagonist, exhibiting si… | 100 mg | Q-270 | More Info |
| QNZ 46 | QNZ-46 is a potent, noncompetitive NMDA receptor antagonist, exhibiting si… | 25 mg | Q-270 | More Info |
| QNZ 46 | QNZ-46 is a potent, noncompetitive NMDA receptor antagonist, exhibiting si… | 5 mg | Q-270 | More Info |
| QNZ 46 | QNZ-46 is a potent, noncompetitive NMDA receptor antagonist, exhibiting si… | 50 mg | Q-270 | More Info |
| QO-40 | QO-40 is a KCNQ channel opener with EC50 of ~7 µM on cloned channels… | 10 mg | Q-265 | More Info |
| QO-40 | QO-40 is a KCNQ channel opener with EC50 of ~7 µM on cloned channels… | 25 mg | Q-265 | More Info |
| QO-40 | QO-40 is a KCNQ channel opener with EC50 of ~7 µM on cloned channels… | 5 mg | Q-265 | More Info |
| Quin-C7 | Quin-C7 is a nonpeptide antagonist of N-formyl peptide receptor 2 (FPR2, F… | 10 mg | Q-155 | More Info |
| Quin-C7 | Quin-C7 is a nonpeptide antagonist of N-formyl peptide receptor 2 (FPR2, F… | 25 mg | Q-155 | More Info |
| Quin-C7 | Quin-C7 is a nonpeptide antagonist of N-formyl peptide receptor 2 (FPR2, F… | 5 mg | Q-155 | More Info |
| Quin-C7 | Quin-C7 is a nonpeptide antagonist of N-formyl peptide receptor 2 (FPR2, F… | 50 mg | Q-155 | More Info |
| QX-314 bromide | QX-314 bromide is an intracellular blocker of NaV channels1-4. Synthetic.… | 1 g | Q-100 | More Info |
| QX-314 bromide | QX-314 bromide is an intracellular blocker of NaV channels1-4. Synthetic.… | 100 mg | Q-100 | More Info |
| QX-314 bromide | QX-314 bromide is an intracellular blocker of NaV channels1-4. Synthetic.… | 2.5 g | Q-100 | More Info |
| QX-314 bromide | QX-314 bromide is an intracellular blocker of NaV channels1-4. Synthetic.… | 500 mg | Q-100 | More Info |
| QX-222 chloride | QX-222 chloride blocks NaV currents1 and also inhibits nicotinic ACh recep… | 10 mg | Q-200 | More Info |
| QX-222 chloride | QX-222 chloride blocks NaV currents1 and also inhibits nicotinic ACh recep… | 25 mg | Q-200 | More Info |
| QX-222 chloride | QX-222 chloride blocks NaV currents1 and also inhibits nicotinic ACh recep… | 50 mg | Q-200 | More Info |
| QX-314 chloride | QX-314 chloride is an intracellular blocker of NaV channels1-4. Synthetic.… | 1 g | Q-150 | More Info |
| QX-314 chloride | QX-314 chloride is an intracellular blocker of NaV channels1-4. Synthetic.… | 100 mg | Q-150 | More Info |
| QX-314 chloride | QX-314 chloride is an intracellular blocker of NaV channels1-4. Synthetic.… | 50 mg | Q-150 | More Info |
| QX-314 chloride | QX-314 chloride is an intracellular blocker of NaV channels1-4. Synthetic.… | 500 mg | Q-150 | More Info |
| R214127 | R214127 is a potent and selective non-competitive antagonist of mGluR1 rec… | 10 mg | R-215 | More Info |
| R214127 | R214127 is a potent and selective non-competitive antagonist of mGluR1 rec… | 25 mg | R-215 | More Info |
| R214127 | R214127 is a potent and selective non-competitive antagonist of mGluR1 rec… | 5 mg | R-215 | More Info |
| R214127 | R214127 is a potent and selective non-competitive antagonist of mGluR1 rec… | 50 mg | R-215 | More Info |
| Rabbit IgG Isotype Control-APC | A Rabbit isotype control antibody conjugated to the fluorescent dye Alloph… | 50 µl | RIC-001-APC | More Info |
| Rabbit IgG Isotype Control-FITC | A Rabbit isotype control antibody conjugated to the fluorescent dye FITC | 50 µl | RIC-001-F | More Info |
| Rabbit IgG Isotype Control-PE | A Rabbit isotype control antibody conjugated to the fluorescent dye Phycoe… | 50 µl | RIC-001-PE | More Info |
| Radicicol | Radicicol is an antifungal antibiotic originally discovered to be a tyrosi… | 0.5 mg | R-370 | More Info |
| Radicicol | Radicicol is an antifungal antibiotic originally discovered to be a tyrosi… | 1 mg | R-370 | More Info |
| Radicicol | Radicicol is an antifungal antibiotic originally discovered to be a tyrosi… | 5 x 1 mg | R-370 | More Info |
| Ralfinamide mesylate | Ralfinamide mesylate is a Na+ channel blocker1. Its IC50 values for tonic… | 25 mg | R-105 | More Info |
| Ralfinamide mesylate | Ralfinamide mesylate is a Na+ channel blocker1. Its IC50 values for tonic… | 5 mg | R-105 | More Info |
| Ralfinamide mesylate | Ralfinamide mesylate is a Na+ channel blocker1. Its IC50 values for tonic… | 50 mg | R-105 | More Info |
| Ralfinamide mesylate | Ralfinamide mesylate is a Na+ channel blocker1. Its IC50 values for tonic… | 10 mg | R-105 | More Info |
| 3Rα-Pompilidotoxin | 3Rα-Pompilidotoxin slows NaV channel inactivation without changing t… | 1 mg | P-174 | More Info |
| 3Rα-Pompilidotoxin | 3Rα-Pompilidotoxin slows NaV channel inactivation without changing t… | 10 mg | P-174 | More Info |
| 3Rα-Pompilidotoxin | 3Rα-Pompilidotoxin slows NaV channel inactivation without changing t… | 5 mg | P-174 | 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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