| Description | Product descriptionCompositionStorage Conditions50T100TSolution ARoom temperature100mL200mLDetox BRoom temperature25g50gAfter the product is received, store the ingredients at the temperature indicated above, and it will be valid for 12 months. Ethidium bromide (EB) Ames test results show that EB Product descriptionCompositionStorage Conditions50T100TSolution ARoom temperature100mL200mLDetox BRoom temperature25g50gAfter the product is received, store the ingredients at the temperature indicated above, and it will be valid for 12 months. Ethidium bromide (EB) Ames test results show that EB can easily cause mutations in organisms. Powerful EB Detoxifier is a product specially designed to remove ethidium bromide (EB) pollution. It can effectively destroy the structure of EB and remove the carcinogenicity of EB, thereby achieving the purpose of cleaning EB pollution. It is suitable for removing EB contamination of electrophoresis buffer, biochemical solution and solid surface (such as laboratory bench, centrifuge, glassware, stainless steel products, etc.). After using a powerful EB detoxifier to treat EB pollutants, then discarding it can protect the environment from EB pollutants.Product performance indexIt can destroy the structure of EB, eliminate the fluorescence of EB, and reduce its mutagenicity by more than 99.5%.Precautions1. Solution A is corrosive, and to protect your safety during the operation of EB, please wear gloves and goggles.2. There may be a small amount of irritating and harmful gas generated during the chemical reagent preparation and processing of EB, please operate in a fume hood.3. There is no method that can eliminate EB 100%, so even after handling, you should wear gloves and handle it carefully, not as 100% safe. If conditions permit, it is best to regularly test for mutagenicity to ensure the correctness of the treatment process.Operation steps: (Please read the notes before experiment)1. Treatment of various pollution solutions (100mL EB pollution solution)1) Ensure that the concentration of EB in various polluted solutions does not exceed 0.5mg/mL. If the concentration is too high, first dilute with water to meet the required concentration.2) Preparation of working solution: In a fume hood, dilute 2 mL of solution A with deionized water to a final volume of 20 mL for use. Dissolve 0.42 g of detoxifier B in water and dilute to 12 mL for use.3) Add the above 20mL solution A working solution and 12mL detoxifier B working solution to 100mL EB contaminated solution, stir and mix carefully (make sure pH≤3).4) Allow to react at room temperature for 24 hours, adjust the pH to 5-9 with sodium bicarbonate.5) Wash the reactants into the water tank with a lot of water for disposal.2. Various solid surface pollution treatment1) Preparation of working solution: In a fume hood, add 4.2g of detoxifier B to 300mL of deionized water, add 20mL of solution A after fully dissolving, stir and mix carefully (pH is about 1.8).2) After ensuring that the electrical appliances are in a power-off state, soak the freshly prepared working fluid with a paper towel, carefully wipe clean the contaminated surface, repeat 6 times, each time change to a new paper towel soaked in the working fluid, and finally soak it clean Wipe clean the working fluid with paper towels of deionized water, and collect the paper towels into a designated processing container. The pH value of the working fluid is 1.8, which is slightly corrosive. It is not suitable for wiping items with weak tolerance. You can use paper towels soaked in deionized water to wipe. Before wiping, a UV lamp can be used to help find the contaminated area. After wiping, it can help confirm that it has been wiped clean.3) Soak these contaminated paper towels in the working fluid at room temperature for at least one hour. After adjusting the pH to 5-9 with sodium bicarbonate, the liquid is flushed into the sink with plenty of water, and the paper towels are put into the garbage dump... Read More | Amine-Reactive probe which passively diffuse into cells and it is nonfluorescent until the acetate groups are cleaved by intracellular esterases to yield the highly fluorescent, amine-reactive fluorophore. Upon reaction with amine-containing residues of intracellular proteins, these probes form dye Amine-Reactive probe which passively diffuse into cells and it is nonfluorescent until the acetate groups are cleaved by intracellular esterases to yield the highly fluorescent, amine-reactive fluorophore. Upon reaction with amine-containing residues of intracellular proteins, these probes form dye protein adducts that are well retained in cells as they move and divide during embryonic development.A Non-fluorescent cell permeant amine-reactive probe for long term tracing of cell... Read More | Laccase is an enzyme, produced by ericoid mycorrhiza and ectomycorrhiza fungi. It belongs to the group of polyphenol oxidases. Laccase is also present in plants and bacteria.Laccase from Trametes versicolor has been used: to assess the use of four laccase-producing strains in waste water treatment Laccase is an enzyme, produced by ericoid mycorrhiza and ectomycorrhiza fungi. It belongs to the group of polyphenol oxidases. Laccase is also present in plants and bacteria.Laccase from Trametes versicolor has been used: to assess the use of four laccase-producing strains in waste water treatment in laccase assay in screening the lignolsSome of the enzymatic actions of laccase are associated with sporulation, detoxification, morphogenesis, melanin polymerization and it offers protection to spore coat. Laccase can catalyse a number of substrates including medicinal drugs and halogenated pesticides. It utilizes oxygen for its catalysis. For these reasons, it might be useful in the biological degradation of micropollutants in wastewater treatment. Laccase catalyzes the oxidation of phenol containing compounds, including lignin, through the reduction of oxygen to water. The presence of mediators will allow the oxidation of non-phenlic compounds as well. The primary function of laccase is to degrade lignin in fungi... Read More | Aprotinin is a competitive serine protease inhibitor that inhibits trypsin,chymotrypsin,kallikrein and plasmin.Aprotinin forms stable complexes with and blocks the active sites of enzymes. Binding is reversible with most aprotinin,protease complexes and dissociating at pH >10 or <3. Effective Aprotinin is a competitive serine protease inhibitor that inhibits trypsin,chymotrypsin,kallikrein and plasmin.Aprotinin forms stable complexes with and blocks the active sites of enzymes. Binding is reversible with most aprotinin,protease complexes and dissociating at pH >10 or <3. Effective concentration is equimolar with protease.Recombinant aprotinin is expressed in E. Coli, and purified with HPLC. It contains no animal-derived components. This is a recombinant form of bovine lung aprotinin, which is traditionally isolated from bovine lung by methods involving fractional precipitation, gel filtration, and ion exchange chromatography. UNIT DEFINITION:A conversion factor for Aprotinin is: 1 EPU = 1 USP Aprotinin Unit = 1800 KIU... Read More | Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue StainingDescription:MCP-2 and CCL7 are two monocyte chemotactic proteins produced by human MG-63 osteosarcoma cells. Both MCP-2 and CCL7 are members of the C-C family of chemokines and share 62% and 71% amino acid sequence identity, Purity:>95%, by SDS-PAGE visualized with Coomassie® Blue StainingDescription:MCP-2 and CCL7 are two monocyte chemotactic proteins produced by human MG-63 osteosarcoma cells. Both MCP-2 and CCL7 are members of the C-C family of chemokines and share 62% and 71% amino acid sequence identity, respectively, with MCP-1. CCL7 also shares 58% amino acid identity with MCP-2. CCL7 cDNA encodes a 99 amino acid residue precursor protein from which the N-terminal 23 amino acid residues are cleaved to generate the 76 amino acid residue mature CCL7. Mature CCL7 contains a potential N-linked and several possible O-linked glycosylation sites. Similarly to other C-C chemokines, all three MCP proteins are monocyte chemoattractants. In addition, the three MCPs can chemoattract activated NK cells as well as CD4+ and CD8+ T lymphocytes. All three cytokines have also been shown to attract eosinophils and induce histamine secretion from basophils... Read More |