Indoleacetic acid oxidase Assay Kit
Product Name: Magnesium L-Threonate Type: Food Additives Origin: China CAS No.: 778571-57-6 AUCO No.: 424 Packing: 25kg/drum Items Standard Appearance The product is white fine granular powder, odorless and tasteless. Identification Add ammonia-ammonium chloride buffer to the aqueoussolution, add chromium black T Reagent, generate thewine red; then add EDTA,generate the pure blue. Clarity Take 0.lg of this product, dissolve in water to 10ml, shake and observe whether the solution is clear. Assay (on thedried basis) 98.0%~102.0% Mg2 7.2%~8.3% Water 1.0% NH 6.0~8.0 Density (Tap density) 0.6g/mL Density (Bulk density)0.4g/mL Heavy metal (As) 0.06ppm Heavy metal (Pb) 0.02ppm Heavy metal (Hg) 0.25ppm Micro-Organism (Total Bacteria Count) 1000CFU/g Micro-Organism (E.Coli) 40MPN/100g Micro-Organism (Yeast&Mold) 25CFU/g Micro-Organism (Pathogenic bacteria) Negative
This kit is used to qualitatively detect the novel coronaviruses (SARS-CoV-2) antigen in human nasal throat swabs, oral throat swabs, posterior oropharyngeal saliva, sputum and stool samples.
Cat. No. - PB102-01 Packing - 1kit+C5:C53 Price - 20580
SARS-CoV-2 Antigen Assay Kit (Colloidal Gold Method) This kit is used for the qualitative detection of specific antigen against novel coronavirus (SARS-CoV-2) in human specimens (Nasal swabs, oropharyngeal swabs, lower respiratory tract samples). Principle This kit adopts colloidal gold-based flow-through, lateral-flow immunoassay and capture method to detect specific antigen against coronavirus in human specimens(Nasal swabs, oropharyngeal swabs.
Cat No : 09N77-095. The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria.
The second brand in the world health organization test list Colloidal Gold Method This kit applies the principle lateral flow chromatographic immunoassay and uses capture method to detect specific IgM and IgG antibodies against novel coronavirus in human specimens (serum, plasma and venous whole blood).
Isocyanuric Acid also known as Cyanuric Acid is a white odorless solid. Its an industrial chemical that is used as a raw material and precursor to prepare cyanuric acid bromide, chloride, iodine chloride, bromo chloride, and its cyanurate ester which are used to manufacture , bleaches, paints, herbicides, plastic, nylon, resin, chlorine stabilizer, chlorinating/bromination agents, antioxidants, metal cyanide mitigants and polyester flame retardant. Isocyanuric Acid (Cyanuric Acid) 09-020-01 Sales Specification Assay (%): 98.5 Min PH (1% Solution): 2.8 Min Moisture, %: 0.5 Max Residue of Ignition (Ash), %: 0.1 Max Ferric Content, PPM: 10 Max Concentration of Ammelide & Ammeline, %: 0.5 Max Ammonia, PPM: 20 - 200 Packing 55.115 lb pail, 18 pails per pallet.
Nickel chloride hexahydrate is a high-purity chemical compound used in various industries such as electroplating, catalyst manufacturing, material science, electronics, pharmaceutical research and organic synthesis. Nickle Chloride Hexahydrate is also used as a catalyst for making dialkyl arylphosphonates. Nickel Chloride Hexahydrate, is used as a reagent in nickel electroplating, as an anode activator in rapid nickel plating, and as an ammonia absorber in industrial or gas masks. For the manufacture of catalysts, dry batteries. Creates invisible ink. Nickle Chloride Hexahydrate is also used in Electroforming, Electroless Plating, Dye mordant, Insecticides, Glass colorant and other chemicals. Nickle Chloride Solution is also known as Nickle Chloride Anhydrous, is used mainly as a plating agent and metal surface treating agent. Nickel Chloride Hexahydrate WC Code: 14-009-01 CAS: 7791-20-0 Molecular Formula: NiCl2.6H2O Molecular Weight: 237.70 g/ mol Sales Specification Appearance: Green Crystals Assay: 98% Ni: 24 Co:
Ammonium Hydroxide has various application but its top uses are, as an ingredient in many cleaning products, as a precursor to alkylamines, it is also used as a refrigerant gas because it absorbs heat from its surroundings, it is uses in water and waste water treatment as a stabilizer, it is used in to make ammonium nitrate fertilizer. It is also used for furniture darkening and for treatment of straw for cattle. It is used in the manufacturing of papers, rubbers, ammonia soaps, detergents, pharmaceutical products, fireproofing woods, inks, ceramics, and ammonium compounds. It is also utilized in metal extraction and a neutralizing agent for acids. It is used in the textile industry and a mordant. It is used in cosmetic products to neutralize the acidity of the product. Sales Specifications Assay: 25.00 % Min Specific Gravity: NS (ppm) Carbonate: 0.002 % Max Chloride: 0.5 ppm Max Sulphate: 2 ppm Max Sulphide: 0.1 ppm Max Arsenic: 0.05 ppm Max Iron: 0.2 ppm Max Phosphate: 1 ppm Max Calcium: 4 ppm Max Copper: 0.1 ppm Max Lead: 0.4 ppm Max Magnesium: 4 ppm Max Potassium: NS (ppm) Sodium: NS (ppm) Zinc: Oxygen Absorbed: Passes Test Pyradine & Homologues: Passes Test Silicate (SiO2): 10 ppm Max Residue on Evaporation: NS (ppm) Total Dissolved Solids: NS (ppm) Chemical Oxygen Demands: NS (ppm) Packing 474 Lb. drum, 4 drums per pallet 1984.14 Lb. IBC tote DOT Transportation UN No.: 2672 Proper Shipping Name: Aqueous Ammonia (Ammonium Hydroxide) Hazard Class: 8 Packing Group: III RQ
Calcium Polysulfide Solution is used mainly as a fungicide and fertilizer for the agriculture industry, to control wide range of fungal and other plant diseases in orchards, field crops and horticulture crops; it can also be used in various treatment systems as a metal precipitating agent. Calcium Polysulfide Solution effectively stabilizes and reduces soluble metals. Sales Specifications Appearance: Clear, to red orange liquid Assay:24.0-29.0% Odor:Slight H2S odor Density:1.25-1.29 @ 25�°C Treatment Notes Arsenic: Acid medium only forms various arsenic sulfides; pH>7; arsenic-sulfur compound are insoluble Lead: Wide Range (pH: 4-9); forms lead sulfide Copper: Close to neutral (Optimal pH: 5â??7); forms copper sulfide Zinc: Wide range (pH: 4-9); forms Zinc sulfide Cadmium: Wide range (pH: 4-9); forms cadmium sulfide Molybdenum: Wide range (pH: 4-9); forms molybdenum sulfide Uranium:Wide range (pH: 4-9); forms uranium sulfide Cyanide: Chemical Conversion produces Thiocyanate* *Thiocyanate can be bio-treated, or it can be treated with lime, producing calcium carbonate, gypsum and ammonia. Chromium (Cr VI) can be treated with calcium polysulfide, and the Cr(VI) is reduced to Cr (III), which is then precipitated as chromium hydroxide. While the list above indicates effective treatment may be obtained with system pH near 4.0, TKI has found that product is most stable in systems with pH greater than 5.0, to avoid potential generation of H2S. Packing 220 gallon (2,809 lbs) tote or 5,000 gallon (53,000 lbs) tank of truck 901 Lb tote
Product Name: Surplex(R)-COVID-19 IgM/IgG Rapid test Product Description: Surplex(R)-COVID-19 IgM/IgG Rapid test is a serology test intended for the qualitative detection of IgM and IgG antibodies of the novel coronavirus (the SARS-COV-2 virus) in human serum, plasma or whole blood. It is CE marked and approved in Brazil (ANVISA approved). We are motivated to aggressively price our product and ready to send 20 tests (one box) to qualified buyers for evaluation, free of charge. Price of product: FOB USD $1.50 - $2.50 per test, volume dependent. Product origin : China. Key Specifications/Special Features : - Competitively priced and ready to ship in volume. - Currently shipping in volume to Brazil. - Highly accurate and specific - performance independently confirmed. - Results ready in 15 minutes. - Harmonization System (HS) Code: 382200. - We provide a full support during regulatory application. Minimum Order Size and Packaging details: MOQ: Flexible. Box of 20 or 50 test kits. Storage: 2-30C. Shelf Life: 10 months.
CareStart Covid-19 Antigen Test Kits-Rapid Test Kits Worldwide Shipping Lateral flow assay Detect SARS-CoV-2 nucleocapsid protein antigen Rapid results within 10-15 minutes Intended at POC setting (i.e., inpatient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation For use under the Emergency Use Authorization (EUA) only For in vitro diagnostic use only For prescription use only For use with direct anterior nasal and nasopharyngeal swab specimens Clinical Performance 93.75% PPAa and 99.32% NPAb when used with a nasopharyngeal swab 87.18% PPAa and 100% NPAb when used with anterior nasal swab aPPA: Positive Percent Agreement, bNPA: Negative Percent Agreement.
Assay+ COVID-19 antigen rapid test is authorized with CE marker, the sensitivity is 90%, the specificity is 98.5%. Assay+ Covid 19 antigen rapid test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein of SARS-CoV-2 from the nasopharyngeal swab from the suspected COVID-19 patients within five days of symptom onset. This test is an aid to differentiate Covid 19 virus infection from other respiratory tract infection caused by coronavirus 229E, NL63, OC43 and HKU1, or severe acute respiratory syndrome caused by SARS-CoV and MERS-CoV. The test should be performed in moderate, high or waived complexity tests. This test can also perform for the Point of Care (POC) purpose.
One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces) Cat. No.: RH0301T INTENDED USE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing. PRINCIPLE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary. STORAGE The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch. WARNING AND PRECAUTIONS 1. For in vitro diagnostic use only. 2. Do not use kit beyond the expiration date. 3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures. 4. The test device should not be reused. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. One operating Instruction MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer SPECIMEN COLLECTION AND PREPARATION 1. Collect stool sample by using the sample collection device provided. 2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample. 3. Put the sample collection stick back in the sample collection device and screw together tightly. 4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing. ASSAY PROCEDURE 1. Remove the test device from foil pouch by tearing along the notch. 2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION 3. Shake the sample collection device several times. 4. Holding the sample collection device upright, carefully unscrew the tip of collection device. 5. Squeeze 2-3 drops of the sample solution on the test sample pad. 6. Read the test results in 5 minutes. INTERPRETATION OF RESULTS Negative: Only one colored band appears on the control region (C). No colored band in the test region (T). Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T). Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid Bulk
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid Bulk
