Name | Description | Size | Catalog # | |
---|---|---|---|---|
Kaliotoxin-1 | Kaliotoxin-1 is a potent inhibitor of large conductance Ca2+-activated K+… | 50 µg | STK-370 | More Info |
1Kα-Pompilidotoxin | 1Kα-PMTX slows NaV channel inactivation without changing the peak cu… | 1 mg | P-172 | More Info |
1Kα-Pompilidotoxin | 1Kα-PMTX slows NaV channel inactivation without changing the peak cu… | 10 mg | P-172 | More Info |
1Kα-Pompilidotoxin | 1Kα-PMTX slows NaV channel inactivation without changing the peak cu… | 5 mg | P-172 | More Info |
1Kα-Pompilidotoxin | 1Kα-PMTX slows NaV channel inactivation without changing the peak cu… | 50 mg | P-172 | More Info |
κ-Bungarotoxin | Kappa-bungarotoxin is a postsynaptic neurotoxin that potently binds and in… | 0.1 mg | B-300 | More Info |
κ-Bungarotoxin | Kappa-bungarotoxin is a postsynaptic neurotoxin that potently binds and in… | 0.5 mg | B-300 | More Info |
κ-Bungarotoxin | Kappa-bungarotoxin is a postsynaptic neurotoxin that potently binds and in… | 1 mg | B-300 | More Info |
κ-Bungarotoxin | Kappa-bungarotoxin is a postsynaptic neurotoxin that potently binds and in… | 50 µg | B-300 | More Info |
κ-Conotoxin RIIIJ | κ-Conotoxin RIIIJ is a blocker of KV1.2 channels1. Synthetic peptide… | 0.1 mg | STC-660 | More Info |
κ-Conotoxin RIIIJ | κ-Conotoxin RIIIJ is a blocker of KV1.2 channels1. Synthetic peptide… | 10 µg | STC-660 | More Info |
κ-Conotoxin RIIIJ | κ-Conotoxin RIIIJ is a blocker of KV1.2 channels1. Synthetic peptide… | 5 µg | STC-660 | More Info |
κ-Conotoxin RIIIJ | κ-Conotoxin RIIIJ is a blocker of KV1.2 channels1. Synthetic peptide… | 5 x 10 µg | STC-660 | More Info |
κ-Conotoxin RIIIJ | κ-Conotoxin RIIIJ is a blocker of KV1.2 channels1. Synthetic peptide… | 5 x 5 µg | STC-660 | More Info |
κ-Conotoxin RIIIK | κ-Conotoxin-RIIIK blocks KV1.2 with high potency. Synthetic peptide.… | 0.1 mg | STC-650 | More Info |
κ-Conotoxin RIIIK | κ-Conotoxin-RIIIK blocks KV1.2 with high potency. Synthetic peptide.… | 10 µg | STC-650 | More Info |
κ-Conotoxin RIIIK | κ-Conotoxin-RIIIK blocks KV1.2 with high potency. Synthetic peptide.… | 5 µg | STC-650 | More Info |
κ-Conotoxin RIIIK | κ-Conotoxin-RIIIK blocks KV1.2 with high potency. Synthetic peptide.… | 5 x 10 µg | STC-650 | More Info |
κ-Conotoxin RIIIK | κ-Conotoxin-RIIIK blocks KV1.2 with high potency. Synthetic peptide.… | 5 x 5 µg | STC-650 | More Info |
K252b | K252b is a less potent derivative of K252a and inhibits a variety of kinas… | 5 x 50 µg | K-170 | More Info |
K252b | K252b is a less potent derivative of K252a and inhibits a variety of kinas… | 50 µg | K-170 | More Info |
K252b | K252b is a less potent derivative of K252a and inhibits a variety of kinas… | 0.45 mg | K-170 | More Info |
1Kβ-Pompilidotoxin | 1Kβ-PMTX slows NaV channel inactivation without changing the peak cur… | 1 mg | P-182 | More Info |
1Kβ-Pompilidotoxin | 1Kβ-PMTX slows NaV channel inactivation without changing the peak cur… | 10 mg | P-182 | More Info |
1Kβ-Pompilidotoxin | 1Kβ-PMTX slows NaV channel inactivation without changing the peak cur… | 5 mg | P-182 | More Info |
KCa Channel Blocker Explorer Kit | A Screening Package of KCa Channel Blockers Economically Priced | 15 vials | EK-101 | More Info |
KCa1.1 Channel Modulator Explorer Kit | A Screening Package of KCa1.1 Channel Modulators Economically Priced | 13 vials | EK-132 | More Info |
KCa Channel Opener Explorer Kit | A Screening Package of KCa Channel Openers Economically Priced | 11 vials | EK-201 | More Info |
KCa2-Related Channel Modulator Explorer Kit | A Screening Package of KCa2 Channel Modulators Economically Priced | 9 vials | EK-122 | More Info |
K+ Channel Blockers for Pain Research Explorer Kit | A Screening Package of K+ Channel Blockers for Pain Research Economically… | 14 vials | EK-390 | More Info |
KC 12291 hydrochloride | Orally active voltage-gated Na+ (NaV) channel blocker1-2 with cardioprotec… | 10 mg | K-105 | More Info |
KC 12291 hydrochloride | Orally active voltage-gated Na+ (NaV) channel blocker1-2 with cardioprotec… | 25 mg | K-105 | More Info |
KC 12291 hydrochloride | Orally active voltage-gated Na+ (NaV) channel blocker1-2 with cardioprotec… | 5 mg | K-105 | More Info |
KC 12291 hydrochloride | Orally active voltage-gated Na+ (NaV) channel blocker1-2 with cardioprotec… | 50 mg | K-105 | More Info |
KCNN4 (KCa3.1) Channel Basic Research Pack | All You Need for KCNN4 (KCa3.1) Channel Research | 7 vials | ESB-400 | More Info |
KCNN4 (KCa3.1) Channel Deluxe Research Pack | All You Need for KCNN4 (KCa3.1) Channel Research | 10 vials | ESD-400 | More Info |
KCNN4 (KCa3.1) Channel Premium Research Pack | All You Need for KCNN4 (KCa3.1) Channel Research | 9 vials | ESP-400 | More Info |
KCNN4 (KCa3.1, SK4) Channel Modulator Explorer Kit | A Screening Package of KCNN4 Channel Modulators Economically Priced | 9 vials | EK-133 | More Info |
KCNQ (KV7) Channel Activator Explorer Kit | A Screening Package of KCNQ (KV7) Channel Activators Economically Priced | 5 vials | EK-225 | More Info |
KCNQ (KV7) Channel Basic Research Pack | All You Need for KCNQ (KV7) Channels Research | 14 vials | ESB-503 | More Info |
KCNQ (KV7) Channel Modulator Explorer Kit | A Screening Package of KCNQ (KV7) Channel Modulators Economically Priced | 8 vials | EK-131 | More Info |
Kir Channel Blocker Explorer Kit | A Screening Package of Kir Channel Blockers Economically Priced | 7 vials | EK-112 | More Info |
KN-62 | KN-62 is a potent non-competitive antagonist of the purinergic P2X7 recept… | 1 mg | K-120 | More Info |
KN-62 | KN-62 is a potent non-competitive antagonist of the purinergic P2X7 recept… | 10 mg | K-120 | More Info |
KN-62 | KN-62 is a potent non-competitive antagonist of the purinergic P2X7 recept… | 25 mg | K-120 | More Info |
KN-62 | KN-62 is a potent non-competitive antagonist of the purinergic P2X7 recept… | 5 mg | K-120 | More Info |
KT5720 | KT5720 is a potent and specific inhibitor of PKA (IC50 = 56 nM)1. Semi-syn… | 0.25 mg | K-190 | More Info |
KT5720 | KT5720 is a potent and specific inhibitor of PKA (IC50 = 56 nM)1. Semi-syn… | 0.5 mg | K-190 | More Info |
KT5720 | KT5720 is a potent and specific inhibitor of PKA (IC50 = 56 nM)1. Semi-syn… | 50 µg | K-190 | More Info |
KT5720 | KT5720 is a potent and specific inhibitor of PKA (IC50 = 56 nM)1. Semi-syn… | 0.1 mg | K-190 | More Info |
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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