Name | Description | Size | Catalog # | |
---|---|---|---|---|
KT5823 | KT5823 is a selective and potent inhibitor of PKG (IC50 = 234 nM)1,2. Semi… | 5 x 50 µg | K-250 | More Info |
KT5823 | KT5823 is a selective and potent inhibitor of PKG (IC50 = 234 nM)1,2. Semi… | 50 µg | K-250 | More Info |
KT5823 | KT5823 is a selective and potent inhibitor of PKG (IC50 = 234 nM)1,2. Semi… | 0.1 mg | K-250 | More Info |
KTX-Sp2 | KTX-Sp2 is a potent blocker of Kv1.3 voltage-gated K+ channels and a weake… | 0.1 mg | STK-050 | More Info |
KTX-Sp2 | KTX-Sp2 is a potent blocker of Kv1.3 voltage-gated K+ channels and a weake… | 0.5 mg | STK-050 | More Info |
KTX-Sp2 | KTX-Sp2 is a potent blocker of Kv1.3 voltage-gated K+ channels and a weake… | 1 mg | STK-050 | More Info |
KTX-Sp2 | KTX-Sp2 is a potent blocker of Kv1.3 voltage-gated K+ channels and a weake… | 10 mg | STK-050 | More Info |
KTX-Sp2 | KTX-Sp2 is a potent blocker of Kv1.3 voltage-gated K+ channels and a weake… | 5 mg | STK-050 | More Info |
Kurtoxin | Kurtoxin is a CaV3.1 and CaV3.2 channel blocker1,2. Synthetic peptide. Pur… | 0.1 mg | STK-800 | More Info |
Kurtoxin | Kurtoxin is a CaV3.1 and CaV3.2 channel blocker1,2. Synthetic peptide. Pur… | 0.5 mg | STK-800 | More Info |
Kurtoxin | Kurtoxin is a CaV3.1 and CaV3.2 channel blocker1,2. Synthetic peptide. Pur… | 25 µg | STK-800 | More Info |
Kurtoxin | Kurtoxin is a CaV3.1 and CaV3.2 channel blocker1,2. Synthetic peptide. Pur… | 50 µg | STK-800 | More Info |
KV4 Channel Basic Research Pack | All You Need for KV4 Channel Research | 7 vials | ESB-502 | More Info |
KV2 Channel Blocker Explorer Kit | A Screening Package of KV2 Channel Blockers Economically Priced | 5 vials | EK-220 | More Info |
KV4 Channel Blocker Explorer Kit | A Screening Package of KV4 Channel Blockers Economically Priced | 9 vials | EK-130 | More Info |
KV Channel Blockers for Pain Research Explorer Kit | A Screening Package of KV Channel Blockers for Pain Research Economically… | 9 vials | EK-380 | More Info |
KV4 Channel Deluxe Research Pack | All You Need for KV4 Channel Research | 13 vials | ESD-502 | More Info |
KV4 Channel Premium Research Pack | All You Need for KV4 Channel Research | 9 vials | ESP-502 | More Info |
KV1.2 (KCNA2) Channel Antibody and Membrane Fractions Kit | Kit Contains Anti-KV1.2 (KCNA2) Antibody and all Controls Necessary for Ro… | 2 vials | LK-101 | More Info |
KV1.2 (KCNA2) Channel Basic Research Pack | All You Need for KV1.2 (KCNA2) Channel Research | 6 vials | ESB-500 | More Info |
KV1.3 (KCNA3) Channel Basic Research Pack | All You Need for KV1.3 (KCNA3) Channel Research | 6 vials | ESB-501 | More Info |
KV1.2 (KCNA2) Channel Deluxe Research Pack | All You Need for KV1.2 (KCNA2) Channel Research | 9 vials | ESD-500 | More Info |
KV1.3 (KCNA3) Channel Deluxe Research Pack | All You Need for KV1.3 (KCNA3) Channel Research | 11 vials | ESD-501 | More Info |
KV1.2 (KCNA2) Channel Premium Research Pack | All You Need for KV1.2 (KCNA2) Channel Research | 8 vials | ESP-500 | More Info |
KV1.3 (KCNA3) Channel Premium Research Pack | All You Need for KV1.3 (KCNA3) Channel Research | 10 vials | ESP-501 | More Info |
Kynurenic acid | Kynurenic acid antagonizes ionotropic glutamate receptors with IC50 values… | 1 g | K-110 | More Info |
Kynurenic acid | Kynurenic acid antagonizes ionotropic glutamate receptors with IC50 values… | 10 g | K-110 | More Info |
Kynurenic acid | Kynurenic acid antagonizes ionotropic glutamate receptors with IC50 values… | 5 g | K-110 | More Info |
L-651,582 | L-651,582 inhibits CaV channels as well as receptor activated Ca2+ signals… | 10 mg | L-110 | More Info |
L-651,582 | L-651,582 inhibits CaV channels as well as receptor activated Ca2+ signals… | 25 mg | L-110 | More Info |
L-651,582 | L-651,582 inhibits CaV channels as well as receptor activated Ca2+ signals… | 5 mg | L-110 | More Info |
L-651,582 | L-651,582 inhibits CaV channels as well as receptor activated Ca2+ signals… | 50 mg | L-110 | More Info |
L-689,560 | L-689,560 is a potent and selective antagonist at the glycine site of NMDA… | 10 mg | L-225 | More Info |
L-689,560 | L-689,560 is a potent and selective antagonist at the glycine site of NMDA… | 25 mg | L-225 | More Info |
L-689,560 | L-689,560 is a potent and selective antagonist at the glycine site of NMDA… | 5 mg | L-225 | More Info |
L-689,560 | L-689,560 is a potent and selective antagonist at the glycine site of NMDA… | 50 mg | L-225 | More Info |
L-701,324 | L-701,324 is a potent and selective NMDA receptor antagonist that acts at… | 10 mg | L-195 | More Info |
L-701,324 | L-701,324 is a potent and selective NMDA receptor antagonist that acts at… | 100 mg | L-195 | More Info |
L-701,324 | L-701,324 is a potent and selective NMDA receptor antagonist that acts at… | 25 mg | L-195 | More Info |
L-701,324 | L-701,324 is a potent and selective NMDA receptor antagonist that acts at… | 50 mg | L-195 | More Info |
Lamotrigine | Lamotrigine has an apparent KD value for inactivated-state block of rat br… | 1 g | L-205 | More Info |
Lamotrigine | Lamotrigine has an apparent KD value for inactivated-state block of rat br… | 100 mg | L-205 | More Info |
Lamotrigine | Lamotrigine has an apparent KD value for inactivated-state block of rat br… | 250 mg | L-205 | More Info |
Lamotrigine | Lamotrigine has an apparent KD value for inactivated-state block of rat br… | 50 mg | L-205 | More Info |
L-AP4 | L-AP4 is a group III mGluR specific agonist. Reversibly depresses basal sy… | 1 mg | L-150 | More Info |
L-AP4 | L-AP4 is a group III mGluR specific agonist. Reversibly depresses basal sy… | 10 mg | L-150 | More Info |
L-AP4 | L-AP4 is a group III mGluR specific agonist. Reversibly depresses basal sy… | 25 mg | L-150 | More Info |
L-AP4 | L-AP4 is a group III mGluR specific agonist. Reversibly depresses basal sy… | 5 mg | L-150 | More Info |
L-AP4 | L-AP4 is a group III mGluR specific agonist. Reversibly depresses basal sy… | 50 mg | L-150 | More Info |
L-Ascorbic acid | IC50 of 6.5 µM on T-type current of rat DRG neurons1. IC50s of 10 an… | 10 g | L-140 | More Info |
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