ALOMONE LABS Non-Antibody Products — page 18 of 36
Non-Antibody Products
Page 18 of 36
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| L-Ascorbic acid | IC50 of 6.5 µM on T-type current of rat DRG neurons1. IC50s of 10 an… | 100 g | L-140 | More Info |
| L-Ascorbic acid | IC50 of 6.5 µM on T-type current of rat DRG neurons1. IC50s of 10 an… | 25 g | L-140 | More Info |
| L-Ascorbic acid | IC50 of 6.5 µM on T-type current of rat DRG neurons1. IC50s of 10 an… | 50 g | L-140 | More Info |
| LASSBio-1135 | LASSBio-1135 is a TRPV1 channel and a TNF-α receptor antagonist1. Sy… | 10 mg | L-190 | More Info |
| LASSBio-1135 | LASSBio-1135 is a TRPV1 channel and a TNF-α receptor antagonist1. Sy… | 25 mg | L-190 | More Info |
| LASSBio-1135 | LASSBio-1135 is a TRPV1 channel and a TNF-α receptor antagonist1. Sy… | 5 mg | L-190 | More Info |
| LASSBio-1135 | LASSBio-1135 is a TRPV1 channel and a TNF-α receptor antagonist1. Sy… | 50 mg | L-190 | More Info |
| Lemborexant | Lemborexant is a potent and selective dual orexin receptor antagonist (IC5… | 10 mg | L-255 | More Info |
| Lemborexant | Lemborexant is a potent and selective dual orexin receptor antagonist (IC5… | 25 mg | L-255 | More Info |
| Lemborexant | Lemborexant is a potent and selective dual orexin receptor antagonist (IC5… | 5 mg | L-255 | More Info |
| Lemborexant | Lemborexant is a potent and selective dual orexin receptor antagonist (IC5… | 50 mg | L-255 | More Info |
| Leptomycin B | Leptomycin B, an unsaturated, branched fatty-acid chain, is an antifungal… | 1 µg | L-500 | More Info |
| Leptomycin B | Leptomycin B, an unsaturated, branched fatty-acid chain, is an antifungal… | 5 µg | L-500 | More Info |
| Leptomycin B | Leptomycin B, an unsaturated, branched fatty-acid chain, is an antifungal… | 5 x 1 µg | L-500 | More Info |
| Lercanidipine hydrochloride | 10 µM were effective in abolishing Ang II mediated smooth muscle con… | 10 mg | L-115 | More Info |
| Lercanidipine hydrochloride | 10 µM were effective in abolishing Ang II mediated smooth muscle con… | 25 mg | L-115 | More Info |
| Lercanidipine hydrochloride | 10 µM were effective in abolishing Ang II mediated smooth muscle con… | 5 mg | L-115 | More Info |
| Lercanidipine hydrochloride | 10 µM were effective in abolishing Ang II mediated smooth muscle con… | 50 mg | L-115 | More Info |
| Lerisetron | Lerisetron inhibits the 5-HT-induced Bezold-Jarisch reflex in anesthetized… | 10 mg | L-175 | More Info |
| Lerisetron | Lerisetron inhibits the 5-HT-induced Bezold-Jarisch reflex in anesthetized… | 25 mg | L-175 | More Info |
| Lerisetron | Lerisetron inhibits the 5-HT-induced Bezold-Jarisch reflex in anesthetized… | 5 mg | L-175 | More Info |
| Lerisetron | Lerisetron inhibits the 5-HT-induced Bezold-Jarisch reflex in anesthetized… | 50 mg | L-175 | More Info |
| Lidocaine | Lidocaine is a commonly used local anesthetic as well as an antiarrythmic… | 10 g | L-105 | More Info |
| Lidocaine | Lidocaine is a commonly used local anesthetic as well as an antiarrythmic… | 25 g | L-105 | More Info |
| Lidocaine | Lidocaine is a commonly used local anesthetic as well as an antiarrythmic… | 50 g | L-105 | More Info |
| Lidocaine hydrochloride | Lidocaine blocks both TTX-sensitive and TTX-resistant NaV channels in DRG… | 50 g | L-145 | More Info |
| Lidocaine hydrochloride | Lidocaine blocks both TTX-sensitive and TTX-resistant NaV channels in DRG… | 25 g | L-145 | More Info |
| Ligustilide | Ligustilide activates TRPA1 with an EC50 of 44 µM1. Natural. Purity… | 10 mg | L-170 | More Info |
| Ligustilide | Ligustilide activates TRPA1 with an EC50 of 44 µM1. Natural. Purity… | 100 mg | L-170 | More Info |
| Ligustilide | Ligustilide activates TRPA1 with an EC50 of 44 µM1. Natural. Purity… | 25 mg | L-170 | More Info |
| Ligustilide | Ligustilide activates TRPA1 with an EC50 of 44 µM1. Natural. Purity… | 50 mg | L-170 | More Info |
| Linopirdine | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 10 mg | L-155 | More Info |
| Linopirdine | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 25 mg | L-155 | More Info |
| Linopirdine | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 5 mg | L-155 | More Info |
| Linopirdine | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 50 mg | L-155 | More Info |
| Linopirdine dihydrochloride | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 10 mg | L-156 | More Info |
| Linopirdine dihydrochloride | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 25 mg | L-156 | More Info |
| Linopirdine dihydrochloride | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 5 mg | L-156 | More Info |
| Linopirdine dihydrochloride | Linopirdine blocks KCNQ channels with an IC50 of 2.4 µM for KV7.2 /… | 50 mg | L-156 | More Info |
| (-)-Lobeline hydrochloride | (-)-Lobeline hydrochloride is a high affinity modulator of nicotinic acety… | 1 g | L-120 | More Info |
| (-)-Lobeline hydrochloride | (-)-Lobeline hydrochloride is a high affinity modulator of nicotinic acety… | 100 mg | L-120 | More Info |
| (-)-Lobeline hydrochloride | (-)-Lobeline hydrochloride is a high affinity modulator of nicotinic acety… | 250 mg | L-120 | More Info |
| Lomerizine dihydrochloride | Lomerizine dihydrochloride inhibited CaV currents in PC12 cells with IC50… | 1 g | L-125 | More Info |
| Lomerizine dihydrochloride | Lomerizine dihydrochloride inhibited CaV currents in PC12 cells with IC50… | 100 mg | L-125 | More Info |
| Lomerizine dihydrochloride | Lomerizine dihydrochloride inhibited CaV currents in PC12 cells with IC50… | 50 mg | L-125 | More Info |
| Lomerizine dihydrochloride | Lomerizine dihydrochloride inhibited CaV currents in PC12 cells with IC50… | 500 mg | L-125 | More Info |
| Loperamide hydrochloride | Loperamide hydrochloride inhibits (IC50 = 2.5 µM) HVA CaV in hippoca… | 10 g | L-100 | More Info |
| Loperamide hydrochloride | Loperamide hydrochloride inhibits (IC50 = 2.5 µM) HVA CaV in hippoca… | 25 g | L-100 | More Info |
| Loperamide hydrochloride | Loperamide hydrochloride inhibits (IC50 = 2.5 µM) HVA CaV in hippoca… | 5 g | L-100 | More Info |
| Loperamide hydrochloride | Loperamide hydrochloride inhibits (IC50 = 2.5 µM) HVA CaV in hippoca… | 50 mg | L-100 | More Info |
| Lorazepam | Lorazepam is a positive allosteric modulator of GABA(A) receptors at the b… | 10 mg | L-230 | More Info |
| Lorazepam | Lorazepam is a positive allosteric modulator of GABA(A) receptors at the b… | 100 mg | L-230 | More Info |
| Lorazepam | Lorazepam is a positive allosteric modulator of GABA(A) receptors at the b… | 25 mg | L-230 | More Info |
| Lorazepam | Lorazepam is a positive allosteric modulator of GABA(A) receptors at the b… | 50 mg | L-230 | More Info |
| Lorcainide HCl | Lorcainide is a Na+ channel blocker, which is used as an antiarrhythmic dr… | 10 mg | L-135 | More Info |
| Lorcainide HCl | Lorcainide is a Na+ channel blocker, which is used as an antiarrhythmic dr… | 25 mg | L-135 | More Info |
| Lorcainide HCl | Lorcainide is a Na+ channel blocker, which is used as an antiarrhythmic dr… | 5 mg | L-135 | More Info |
| Lorcainide HCl | Lorcainide is a Na+ channel blocker, which is used as an antiarrhythmic dr… | 50 mg | L-135 | More Info |
| Losartan potassium | Losartan potassium is an Angiotensin II Type 1 receptor antagonist1. Synth… | 1 g | L-185 | More Info |
| Losartan potassium | Losartan potassium is an Angiotensin II Type 1 receptor antagonist1. Synth… | 5 g | L-185 | More Info |
| Losartan potassium | Losartan potassium is an Angiotensin II Type 1 receptor antagonist1. Synth… | 500 mg | L-185 | More Info |
| Lq2 | Lq2 inhibits Kir1.1 K+ inward rectifier channels2, as well as KCa channels… | 0.1 mg | RTL-550 | More Info |
| Lq2 | Lq2 inhibits Kir1.1 K+ inward rectifier channels2, as well as KCa channels… | 10 µg | RTL-550 | More Info |
| Lq2 | Lq2 inhibits Kir1.1 K+ inward rectifier channels2, as well as KCa channels… | 5 µg | RTL-550 | More Info |
| Lq2 | Lq2 inhibits Kir1.1 K+ inward rectifier channels2, as well as KCa channels… | 5 x 10 µg | RTL-550 | More Info |
| Lq2 | Lq2 inhibits Kir1.1 K+ inward rectifier channels2, as well as KCa channels… | 5 x 5 µg | RTL-550 | More Info |
| L-Quisqualic acid | L-Quisqualic acid is a selective AMPA receptor agonist1. Synthetic. Purity… | 1 mg | L-210 | More Info |
| L-Quisqualic acid | L-Quisqualic acid is a selective AMPA receptor agonist1. Synthetic. Purity… | 10 mg | L-210 | More Info |
| L-Quisqualic acid | L-Quisqualic acid is a selective AMPA receptor agonist1. Synthetic. Purity… | 25 mg | L-210 | More Info |
| L-Quisqualic acid | L-Quisqualic acid is a selective AMPA receptor agonist1. Synthetic. Purity… | 5 mg | L-210 | More Info |
| L-Quisqualic acid | L-Quisqualic acid is a selective AMPA receptor agonist1. Synthetic. Purity… | 50 mg | L-210 | More Info |
| L-Serine | L-Serine is a Glycine receptor (GlyR) agonist1-5. Synthetic. Purity 0.995.… | 10 g | S-135 | More Info |
| L-Serine | L-Serine is a Glycine receptor (GlyR) agonist1-5. Synthetic. Purity 0.995.… | 100 g | S-135 | More Info |
| L-Serine | L-Serine is a Glycine receptor (GlyR) agonist1-5. Synthetic. Purity 0.995.… | 25 g | S-135 | More Info |
| L-Serine | L-Serine is a Glycine receptor (GlyR) agonist1-5. Synthetic. Purity 0.995.… | 5 g | S-135 | More Info |
| L-Type CaV Channel Blocker Explorer Kit | A Screening Package of L-Type CaV Channel Blockers Economically Priced | 7 vials | EK-103 | More Info |
| LY 294002 | LY 294002 is a potent and specific cell-permeable inhibitor of Pl3-kinase1… | 5 mg | L-300 | More Info |
| LY 294002 | LY 294002 is a potent and specific cell-permeable inhibitor of Pl3-kinase1… | 1 mg | L-300 | More Info |
| LY278584 | LY278584 is a specifiic 5-HT3 antagonist. 0.1 µM completely blocks 1… | 10 mg | L-180 | More Info |
| LY278584 | LY278584 is a specifiic 5-HT3 antagonist. 0.1 µM completely blocks 1… | 25 mg | L-180 | More Info |
| LY278584 | LY278584 is a specifiic 5-HT3 antagonist. 0.1 µM completely blocks 1… | 5 mg | L-180 | More Info |
| LY278584 | LY278584 is a specifiic 5-HT3 antagonist. 0.1 µM completely blocks 1… | 50 mg | L-180 | More Info |
| LY456066 | LY456066 is a potent antagonist of mGluR1 receptors. It inhibits human mGl… | 10 mg | L-240 | More Info |
| LY456066 | LY456066 is a potent antagonist of mGluR1 receptors. It inhibits human mGl… | 25 mg | L-240 | More Info |
| LY456066 | LY456066 is a potent antagonist of mGluR1 receptors. It inhibits human mGl… | 5 mg | L-240 | More Info |
| LY456066 | LY456066 is a potent antagonist of mGluR1 receptors. It inhibits human mGl… | 50 mg | L-240 | More Info |
| LY 456236 hydrochloride | LY 456236 hydrochloride is an antagonist of mGluR1, selective over mGluR5… | 10 mg | L-235 | More Info |
| LY 456236 hydrochloride | LY 456236 hydrochloride is an antagonist of mGluR1, selective over mGluR5… | 25 mg | L-235 | More Info |
| LY 456236 hydrochloride | LY 456236 hydrochloride is an antagonist of mGluR1, selective over mGluR5… | 5 mg | L-235 | More Info |
| LY 456236 hydrochloride | LY 456236 hydrochloride is an antagonist of mGluR1, selective over mGluR5… | 50 mg | L-235 | More Info |
| Lys-Bradykinin | Lys-Bradykinin is an endogenous nonspecific agonist for the B1 and B2 Brad… | 0.5 mg | GPK-100 | More Info |
| Lys-Bradykinin | Lys-Bradykinin is an endogenous nonspecific agonist for the B1 and B2 Brad… | 1 mg | GPK-100 | More Info |
| Lys-Bradykinin | Lys-Bradykinin is an endogenous nonspecific agonist for the B1 and B2 Brad… | 25 mg | GPK-100 | More Info |
| Lys-Bradykinin | Lys-Bradykinin is an endogenous nonspecific agonist for the B1 and B2 Brad… | 5 mg | GPK-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 0.1 mg | STM-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 0.25 mg | STM-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 0.5 mg | STM-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 1 mg | STM-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 10 mg | STM-100 | More Info |
| Mambalgin-1 | Mambalgin-1 is a blocker of ASIC1 channels1,2. Synthetic peptide. Purity >… | 5 mg | STM-100 | 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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