Non-Antibody Products — page 2 of 44,459
Non-Antibody Products
Page 2 of 44,459
| Name | Description | Size | Catalog # | Supplier | |
|---|---|---|---|---|---|
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 25 mg | A-225 |
 ALOMONE LABS |
More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 250 mg | A-225 |
ALOMONE LABS |
More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 5 mg | A-225 |
ALOMONE LABS |
More Info |
| A 967079 | A 967079 is a blocker of TRPA1 channels and has IC50 values of 67 and 289… | 50 mg | A-225 |
ALOMONE LABS |
More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 1 mg | A-360 |
ALOMONE LABS |
More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 10 mg | A-360 |
ALOMONE LABS |
More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 25 mg | A-360 |
ALOMONE LABS |
More Info |
| A-192621 | A-192621 is a selective antagonist of ET-B endothelin receptors, inhibitin… | 5 mg | A-360 |
ALOMONE LABS |
More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 1 mg | A-600 |
ALOMONE LABS |
More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 mg | A-600 |
ALOMONE LABS |
More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 10 x 1 mg | A-600 |
ALOMONE LABS |
More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 mg | A-600 |
ALOMONE LABS |
More Info |
| A23187 | A23187 is a mobile-carrier Ca2+ ionophore and can cause cell activation, d… | 5 x 5 mg | A-600 |
ALOMONE LABS |
More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 10 mg | A-420 |
ALOMONE LABS |
More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 100 mg | A-420 |
ALOMONE LABS |
More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 25 mg | A-420 |
ALOMONE LABS |
More Info |
| A-740003 | A-740003 is a potent and selective competitive antagonist of P2X7 receptor… | 50 mg | A-420 |
ALOMONE LABS |
More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 10 mg | A-435 |
ALOMONE LABS |
More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 25 mg | A-435 |
ALOMONE LABS |
More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 5 mg | A-435 |
ALOMONE LABS |
More Info |
| A-794278 | A-794278 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 50 mg | A-435 |
ALOMONE LABS |
More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 10 mg | A-105 |
ALOMONE LABS |
More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 100 mg | A-105 |
ALOMONE LABS |
More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 25 mg | A-105 |
ALOMONE LABS |
More Info |
| A-803467 | A-803467 is a potent and selective blocker of the TTX-resistant NaV1.8 cha… | 50 mg | A-105 |
ALOMONE LABS |
More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 10 mg | A-415 |
ALOMONE LABS |
More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 25 mg | A-415 |
ALOMONE LABS |
More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 5 mg | A-415 |
ALOMONE LABS |
More Info |
| A-804598 | A-804598 is a potent and selective, competitive and high-affinity antagoni… | 50 mg | A-415 |
ALOMONE LABS |
More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 10 mg | A-470 |
ALOMONE LABS |
More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 25 mg | A-470 |
ALOMONE LABS |
More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 5 mg | A-470 |
ALOMONE LABS |
More Info |
| A-839977 | A-839977 is a potent and selective antagonist of P2X7 receptors, shown to… | 50 mg | A-470 |
ALOMONE LABS |
More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 10 mg | A-440 |
ALOMONE LABS |
More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 25 mg | A-440 |
ALOMONE LABS |
More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 5 mg | A-440 |
ALOMONE LABS |
More Info |
| A-841720 | A-841720 is a potent and selective noncompetitive mGluR1 antagonist, actin… | 50 mg | A-440 |
ALOMONE LABS |
More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 10 mg | A-390 |
ALOMONE LABS |
More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 25 mg | A-390 |
ALOMONE LABS |
More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 5 mg | A-390 |
ALOMONE LABS |
More Info |
| A-850002 | A-850002 inhibits mGluR1 in rat primary cerebellar granule neurons with an… | 50 mg | A-390 |
ALOMONE LABS |
More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 1 mg | A-195 |
ALOMONE LABS |
More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 10 mg | A-195 |
ALOMONE LABS |
More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 25 mg | A-195 |
ALOMONE LABS |
More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 5 mg | A-195 |
ALOMONE LABS |
More Info |
| A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 50 mg | A-195 |
ALOMONE LABS |
More Info |
| 293A | The HEK 293A cell line is an immortalized line of primary human embryonic… | 1 vial | ABI-TC1333 |
 ACCEGEN BIOTECH |
More Info |
| A10.7 | Derived from metastatic liver tumor (clinical stage IV). | 1 vial | ABC-TC533S |
ACCEGEN BIOTECH |
More Info |
| A-172 | Organ: brain Disease: glioblastoma. | 1 vial | ABC-TC0022 |
ACCEGEN BIOTECH |
More Info |
| A-204 | Human Muscle Rhabdomyosarcoma cell line. The A-204 cell line was establish… | 1 vial | ABC-TC445S |
ACCEGEN BIOTECH |
More Info |