ALOMONE LABS Non-Antibody Products — page 1 of 71

Non-Antibody Products
Page 1 of 71
  • Records 1 - 50 of 3,505
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
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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