
Neuroscience
Neuroscience inhibitors are compounds designed to modulate the activity of specific proteins, enzymes, or receptors within the nervous system. These inhibitors are crucial for studying the molecular mechanisms underlying neural function, synaptic transmission, and neurodegenerative diseases. By targeting neurotransmitter receptors, ion channels, and signaling pathways, neuroscience inhibitors aid in the exploration of brain function and the development of therapeutic strategies for neurological disorders such as Alzheimer's, Parkinson's, and epilepsy. At CymitQuimica, we offer a comprehensive range of high-quality neuroscience inhibitors to support your research in neurobiology, neuropharmacology, and cognitive sciences.
Subcategories of "Neuroscience"
- 5-HT Receptor(1,025 products)
- ACK(1 products)
- AChR(648 products)
- ATP Citrate Lyase(17 products)
- Adrenergic Receptor(3,028 products)
- BACE(37 products)
- Beta Amyloid(231 products)
- CaMK(73 products)
- Cyclooxygenase (COX) Inhibitors(602 products)
- Dopamine Receptor(445 products)
- GABA Receptor(372 products)
- Gamma-secretase(63 products)
- GluR(265 products)
- GlyT(26 products)
- Histamine Receptor(385 products)
- LRRK2(42 products)
- Melatonin Receptor(26 products)
- NMDAR(10 products)
- OX Receptor(42 products)
- Opioid Receptor(327 products)
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Found 5637 products of "Neuroscience"
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Mouse STX2(Syntaxin 2) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse STX2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse STX2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse STX2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse STX2 in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidMouse Glu(Glutamic Acid) ELISA Kit
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Mouse Glu. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse Glu. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse Glu in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidHuman 5-HT(5-Hydroxytryptamine) ELISA Kit
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human 5-HT. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human 5-HT. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human 5-HT in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidAcetylcholine chloride
CAS:Formula:C7H16ClNO2Purity:98%Color and Shape:SolidMolecular weight:181.66044-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione
CAS:Formula:C10H10N2O2SPurity:98%Color and Shape:SolidMolecular weight:222.26364-[4-(1,3-Benzodioxol-5-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]benzamide
CAS:Formula:C22H16N4O3Purity:97%Color and Shape:SolidMolecular weight:384.38741-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-, hydrochloride (1:1)
CAS:Formula:C16H23ClFNOPurity:95%Color and Shape:SolidMolecular weight:299.81132-Quinolinecarboxylic acid, 4-hydroxy-
CAS:Formula:C10H7NO3Purity:98%Color and Shape:SolidMolecular weight:189.16751,3-bis[(9Z)-octadec-9-enoyloxy]propan-2-yl (9Z)-octadec-9-enoate
CAS:Formula:C57H104O6Purity:60%Color and Shape:LiquidMolecular weight:885.4321LOXOPROFEN SODIUM SALT
CAS:Formula:C15H21NaO5Purity:98%Color and Shape:SolidMolecular weight:304.3140Zebrafish GH(Growth Hormone) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Zebrafish GH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Zebrafish GH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Zebrafish GH, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Zebrafish GH in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless Transparentliquid2-(3,4-dimethoxyphenyl)ethan-1-amine
CAS:Formula:C10H15NO2Purity:98%Color and Shape:LiquidMolecular weight:181.2316Ref: IN-DA000Q05
5kgTo inquire50kgTo inquire100kgTo inquire5g24.00€10g27.00€25g28.00€50g31.00€100g46.00€250g73.00€500g124.00€1kg194.00€1,3-Benzodioxole-5-carboxylic acid, 7-hydroxy-, methyl ester
CAS:Formula:C9H8O5Purity:97%Color and Shape:SolidMolecular weight:196.1568Rat NRP2(Neuropilin 2) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat NRP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NRP2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat NRP2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat NRP2 in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidAcamprosate Calcium
CAS:Formula:C10H20CaN2O8S2Purity:97%Color and Shape:SolidMolecular weight:400.4824Human LGI1(Leucine-Rich Glioma-Inactivated Protein 1) ELISA Kit
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human LGI1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LGI1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human LGI1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human LGI1 in the samples is then determined by comparing the OD of the samples to the standard curve.Color and Shape:Colourless TransparentliquidHorse GH(Growth Hormone) ELISA Kit
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Horse GH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse GH. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Horse GH in the samples is then determined by comparing the OD of the samples to the standard curve.

