ALOMONE LABS Non-Antibody Products — page 1 of 36
Non-Antibody Products
Page 1 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 10 mg | A-345 | More Info |
| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 25 mg | A-345 | More Info |
| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 5 mg | A-345 | More Info |
| A 784168 | A 784168 is a potent TRPV1 antagonist, inhibiting human TRPV1 activation b… | 50 mg | A-345 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 10 mg | A-225 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 100 mg | A-225 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 25 mg | A-225 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 250 mg | A-225 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 5 mg | A-225 | More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 50 mg | A-225 | More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 1 mg | A-360 | More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 10 mg | A-360 | More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 25 mg | A-360 | More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 5 mg | A-360 | More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 1 mg | A-600 | More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 mg | A-600 | More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 x 1 mg | A-600 | More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 mg | A-600 | More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 x 5 mg | A-600 | More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 10 mg | A-420 | More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 100 mg | A-420 | More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 25 mg | A-420 | More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 50 mg | A-420 | More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 10 mg | A-435 | More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 25 mg | A-435 | More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 5 mg | A-435 | More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 50 mg | A-435 | More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 10 mg | A-105 | More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 100 mg | A-105 | More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 25 mg | A-105 | More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 50 mg | A-105 | More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 10 mg | A-415 | More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 25 mg | A-415 | More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 5 mg | A-415 | More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 50 mg | A-415 | More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 10 mg | A-470 | More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 25 mg | A-470 | More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 5 mg | A-470 | More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 50 mg | A-470 | More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 10 mg | A-440 | More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 25 mg | A-440 | More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 5 mg | A-440 | More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 50 mg | A-440 | More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 10 mg | A-390 | More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 25 mg | A-390 | More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 5 mg | A-390 | More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 50 mg | A-390 | More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 1 mg | A-195 | More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 10 mg | A-195 | More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 25 mg | A-195 | More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 5 mg | A-195 | More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 50 mg | A-195 | More Info |
| AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 10 mg | A-370 | More Info |
| AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 25 mg | A-370 | More Info |
| AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 5 mg | A-370 | More Info |
| AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 50 mg | A-370 | More Info |
| AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 10 mg | A-410 | More Info |
| AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 25 mg | A-410 | More Info |
| AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 5 mg | A-410 | More Info |
| AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 50 mg | A-410 | More Info |
| 17-AAG | 17-AAG is a less toxic and more stable derivative of the antibiotic Geldan… | 0.1 mg | A-580 | More Info |
| 17-AAG | 17-AAG is a less toxic and more stable derivative of the antibiotic Geldan… | 5 x 0.1 mg | A-580 | More Info |
| AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 0.1 mg | STA-155 | More Info |
| AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 0.5 mg | STA-155 | More Info |
| AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 1 mg | STA-155 | More Info |
| Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 0.1 mg | STA-110 | More Info |
| Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 0.5 mg | STA-110 | More Info |
| Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 1 mg | STA-110 | More Info |
| Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 50 µg | STA-110 | More Info |
| Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 0.1 mg | RTA-400 | More Info |
| Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 10 µg | RTA-400 | More Info |
| Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 µg | RTA-400 | More Info |
| Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 x 10 µg | RTA-400 | More Info |
| Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 x 5 µg | RTA-400 | More Info |
| Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 100 mg | A-150 | More Info |
| Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 25 mg | A-150 | More Info |
| Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 250 mg | A-150 | More Info |
| Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 5 mg | A-150 | More Info |
| Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 50 mg | A-150 | More Info |
| ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 10 mg | A-350 | More Info |
| ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 25 mg | A-350 | More Info |
| ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 5 mg | A-350 | More Info |
| ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 50 mg | A-350 | More Info |
| ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 10 mg | A-450 | More Info |
| ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 25 mg | A-450 | More Info |
| ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 5 mg | A-450 | More Info |
| ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 50 mg | A-450 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.1 mg | STW-100 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.25 mg | STW-100 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.5 mg | STW-100 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 1 mg | STW-100 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 10 mg | STW-100 | More Info |
| ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 5 mg | STW-100 | More Info |
| AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 10 mg | A-375 | More Info |
| AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 25 mg | A-375 | More Info |
| AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 5 mg | A-375 | More Info |
| AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 50 mg | A-375 | More Info |
| Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 0.1 mg | STA-150 | More Info |
| Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 0.5 mg | STA-150 | More Info |
| Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 1 mg | STA-150 | 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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