Monoamine Oxidase Kit

The Monoamine Oxidase Assay Kit provides a convenient fluorimetric means to measure MAO enzyme activity in biological samples. In the assay, MAO reacts with p-tyramine, a substrate for both MAO-A and MAO-B, resulting in the formation of H2O2, which is determined by a fluorimetric method. The assay is simple, sensitive, stable, and high-throughput adaptable. Monoamine Oxidase Assay Kit provides a sensitive and simple fluorometric method for detecting monoamine oxidase activity in purified enzyme preparations at levels as low as 12 µU/mL and in tissue samples with as little as 20 µg protein in a 100 µL assay volume.

Monoamine Oxidase Assay Kit  applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-MAO antibody and an MAO-HRP conjugate. The MAO Assay kit provides a homogeneous luminescent method for measuring monoamine oxidase (MAO) activity from recombinant and native sources and for testing the effects of test compounds on MAO activity. The MAO Assay kit is performed by incubating the MAO enzyme source with a luminogenic MAO substrate. The substrate of the MAO Assay is a derivative of beetle luciferin. Upon reaction with MAO, the derivative is converted into luciferin, which in turn reacts with luciferase to produce light. The amount of light produced is directly proportional to the activity of MAO.

Kinase Assay Kit

Kinase Assay Kit depends on checking ADP arrangement, which is straightforwardly relative to protein phosphotransferase action and is measured fluorimetrically. This protein coupled unit gives a quick, straightforward, and homogeneous examine to gauge kinase exercises. It is a non-radioactive and no wash technique to distinguish the measure of ADP delivered from compound response. Its attributes of high affectability and expansive ATP resistance make it a perfect unit for deciding kinase Michaelis-Menten energy and for screening and recognizing kinase inhibitors. The test can be performed in a helpful 96-well or 384-well microtiter plate position and effectively adjusted to mechanization without a detachment step.

Kinase Activity gives a straightforward, non-radioactive, high-throughput perfect organization for examining the protein action of kinases in vitro. The greater part of kinases use ATP as the phosphate benefactor. They exchange the terminal phosphate gathering of ATP to a substrate, delivering ADP as a by-item. This pack is an ADP-based phosphatase-coupled kinase test that uses CD39L2/ENTPD6 as a coupling phosphatase.The measure of inorganic phosphate discharged is corresponding to the measure of ADP created amid the kinase response and in this way, mirrors the energy of the response.

Glutathione Peroxidase Kit

Glutathione Peroxidase pack assume vital parts in the insurance of creatures from oxidative harm. Glutathione Peroxidase Assay Kit (Colorimetric) is a test where glutathione peroxidase (GPx) decreases the test Cumene Hydroperoxide while oxidizing GSH to GSSG. The created GSSG is lessened to GSH with utilization of NADPH by glutathione reductase (GR). The decline of NADPH (effortlessly measured at OD=340 nm) is relative to GPx action. The test can be utilized to quantify the majority of the glutathione subordinate peroxidases in plasma, erythrocyte lysates, tissue homogenates, and cell lysates with a recognition affectability of ~ 0.5 mU/ml of GPx in tests.

Glutathione peroxidase unit gives an instrument to detoxification of peroxides in living cells. This response assumes an essential part in shielding cells from harm by free radicals, which are framed by peroxide deterioration. Lipid parts of the cell are particularly powerless to responses with free radicals, bringing about lipid peroxidation. GPx proteins lessen peroxides to alcohols utilizing glutathione, in this manner keeping the arrangement of free radicals.

Glucose Assay Kit

Glucose Assay Kit gives direct estimation of glucose in different natural examples (e.g., serum, plasma, body liquid, nourishment, development medium, and so forth.). Glucose Enzyme Mix particularly oxidizes glucose to create an item which responds with a color to produce and fluorescence. The created shading and fluorescence is relatively to the glucose sum. The technique is fast, basic, touchy, and reasonable for high throughput. The measure is likewise appropriate for checking glucose level amid aging and glucose nourishing in protein expression forms. The pack identifies 1-10000 µM glucose tests.

Glucose examine Kit is for the quantitative, enzymatic determination of glucose in nourishment and different materials. Glucose is oxidized to gluconic corrosive and hydrogen peroxide by glucose oxidase. Hydrogen peroxide responds with o-dianisidine within the sight of peroxidase to frame a shaded item. Oxidized o-dianisidine responds with sulfuric corrosive to shape a more steady hued item. The force of the pink shading measured at 540 nm is relative to the first glucose fixation.

Fatty Acid Assay Kit

 BioAssaysys' Fatty Acid Assay Kit gives a helpful, delicate protein based technique for distinguishing the long-chain free unsaturated fats (FA) in different organic specimens, for example, serum, plasma and other body liquids, nourishment, development media, and so on. In this measure, FA are changed over to their CoA subsidiaries (coenzyme A), which are thusly oxidized, prompting arrangement of shading/fluorescence. Unsaturated fats can then be effortlessly evaluated by either colorimetric or fluorometric .

The Fatty Acid Assay Kit is a basic, colorimetric test that quantitatively measures the free unsaturated fat focus (non-esterified) in different specimens utilizing a 96-well microtiter plate position. Every pack gives adequate reagents to perform up to 100 examines, including spaces, norms and obscure examples. The unit contains a palmitic corrosive standard and has an identification affectability point of confinement of ~15 µM. This pack is not appropriate for pee or heparin-containing tests. Unsaturated fats (C8 and more) can be evaluated with this pack.

Fatty Acid Assay Kit

BioAssaysys' Fatty Acid Assay Kit gives a helpful, delicate protein based technique for distinguishing the long-chain free unsaturated fats (FA) in different organic specimens, for example, serum, plasma and other body liquids, nourishment, development media, and so on. In this measure, FA are changed over to their CoA subsidiaries (coenzyme A), which are  oxidized, prompting arrangement of shading/fluorescence. Unsaturated fats can then be effortlessly evaluated by either colorimetric or fluorometric .

The Fatty Acid Assay Kit is a basic, colorimetric test that quantitatively measures the free unsaturated fat focus (non-esterified) in different specimens utilizing a 96-well microtiter plate position. Every pack gives adequate reagents to perform up to 100 examines, including spaces, norms and obscure examples. The unit contains a palmitic corrosive standard and has an identification affectability point of confinement of ~15 µM. This pack is not appropriate for pee or heparin-containing tests. Unsaturated fats (C8 and more) can be evaluated with this pack.