Name Testing kit for New coronavirus (2019-nCOV) IgG/IgM antibody Rapid Test WB/S/P Specifications 25 tests Introduce This kit uses the colloidal gold immunochromatographic principle to qualitatively detect novel coronavirus igg/igm antibodies in human serum, plasma, or whole blood. the sample to be tested was added to the sample hole of the test paper, and then added 2 drops of sample diluent. the igg/igm antibody in the sample combined with the recombinant new coronavirus antigen labeled with the colloidal gold on the binding pad formed complex. under the action of chromatography, it diffused forward along the nitrocellulose membrane (nc membrane). the nitrocellulose membrane was fixed with two detection lines (g line, m line) and one quality control line (c line). the g line was fixed with anti-human igg antibody for the detection of new coronavirus igg antibody; the m line was fixed with anti-human igm antibody for the detection of new coronavirus igm antibody; and the c line had quality control for the detection of the new coronavirus ig antibody. If the sample contains a new coronavirus IgG antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human IgG antibody fixed on the NC membrane detection line (G line). if the sample contains a novel coronavirus igm antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human igm antibody fixed on the nc membrane detection line (m line). The darker the color of the colloidal gold accumulated on the detection line, the higher the concentration of the new coronavirus antibody in the sample. To monitor the effectiveness of the test card, set up a quality control line (line C), whether there is a detection line (line T), quality control line (line C) should be color, otherwise the test results are judged invalid. Storage Stored at 4 to 30c and valid for 18 months. After the aluminum foil bag is unsealed, please use it as soon as possible. Sample 1. It is suitable for human serum, plasma and whole blood samples. 2. The samples should be used as soon as possible; if they cannot be used immediately, the serum / plasma samples should be kept at 2-8C for 5 days and -20C for long-term preservation; the whole blood samples should be placed at 2-8C to avoid hemolysis; 3.The sample contains a large amount of lipids, hemolysis or turbidity, do not use, so as not to affect the judgment of the results.
COV19/ FluA/ FluB Antigen Combo Rapid Test Kit (Colloidal Gold Method) Packing Specifications The kit is an in vitro immunochromatographic assay for the qualitative detection of Cov19, Influenza A and Influenza B virus antigens in human nasopharyngeal, oropharyngeal swab, and salvia samples. Cov19 is an acute respiratory infectious disease that humans are easily infected with. According to current epidemiological investigations, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main symptoms are: fever, fatigue, dry cough, in a few cases can appear nasal congestion, sore throat, myalgia and diarrhea. Influenza, often called the flu is caused by the influenza virus. It is a highly contagious viral infection of the respiratory tract that can be spread by coughing or sneezing. Influenza outbreaks occur every fall and winter. There are influenza A, B and C viruses. Influenza A viruses are more prevalent than influenza B and Cand causes more severe illness. Cov19 infection and Influenza virus infection have similar symptoms, such as fever, cough, etc. This kit can simultaneously detect the antigens of the three viruses and provides an easy workflow, short turnaround time, and rapid diagnosis of Cov19, Influenza A and influenza B virus infections using nasopharyngeal, oropharyngeal swab or salvia samples. The kit is an immunochromatographic assay,based on double antibody sandwich method to detect Cov19 and Influenza A/B virus antigens. This method does not require expensive medical instruments and consumables. After adding the extracted specimen to the sample well on the test cassette, Cov19, Influenza A/B virus antigens in the sample will interact with the colloidal gold-labeled anti-CoV-2 and Influenza A/B antibodies on the conjugate pads. Then the conjugate pad will release re-solubilized conjugate onto the nitrocellulose membrane. The nitrocellulose membrane (NC membrane) diffuses it forward. As the sample moves along the device binding reagents situated on the nitrocellulose membrane bind to the target at the test line. If the sample contains a COV19 antigen, it will bind to the colloidal goldanti-CoV-2 Np monoclonal antibody, diffuse forward, and then react with the anti-CoV-2 Np monoclonal antibody immobilized on the NC membrane detection line (COV19 Test line). Similarly, if the specimen contains Influenza A/Influenza B antigens, the antigens will react with antibody-coated particles, the conjugate migrate laterally forward, and cause a colored lines (A, B linesrespectively).
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Antigen Detection Kit (Colloidal Gold-Based) Key Advantages: â?¢Get result rapidly (10 min), suitable for large-scale screening. â?¢Easy to operate, no instrument needed. â?¢Detect virus directly, faster than PCR test â?¢High accuracy and good consistency with PCR test â?¢Room-temperature storage (4â??- 30â??) Production Description: The double antibody sandwich method is adopted in the product, and measurement is conducted in the form of solid-phase immune chromatography. The sample to be tested will diffuse upwards at the charging end under capillary action, and then SARS-CoV-2 antigen in the sample will combine with the antibody in the marker pad and form colloidal gold antibody-antigen complex; The complex continues to diffuse to the nitrocellulose membrane with the sample, and then blocked by T-line (test line) packed with antibody, and form colloidal gold labeled antibody-antigen-immune complex packed with antibody. The rest unblocked colloidal gold complex continues to move upwards, and combine with C-line (quality control line), indicating that the reaction is completed.
Pigment Violet 23 - Commercial Name - Amilite Fast Violet - Chemical Class Carbazole Dioxazine -Colour Index No. 51319 CAS No. 215247-95-3. Application area: Decorative paints . water and solvent, Industrial paints, Automotive and Auto re-finish Plastic - Polyolefins plastics, PVC and PVC leather cloth &ABS. Platic ink - Heatset, Coldset, Sheetfed, Metal Deco Nitrocellulose Ink water - Alcohol & acetate, Water base, Polyvinyl butyral, Polyamide, Pub gravure, Toluene, UV Ink Textile Printing & Rubber industries. The powder is widely used in industries. We make available our powder in safe packaging of the best quantities. Moreover, we make available our product at the most affordable price. The minimum order quantity of the product is 100kg. We make sure to deliver the orders well on time at the required destination.
Dpmâ is used as solvent for pvc stabilizer, nitrocellulose, ethyl cellulose, polyvinyl acetate, solvent for paint and dyestuff, and an ingredient of brake fluid. It can be used as solvent of printing ink, enamel paint, cutting fluid and operating oil; as coupling agent of water-based paint (usually used by mixing up); as active solvent of water-based paint; as solvent and coupling agent of household and industrial cleanser, remover for grease and paint, cleanser for metal and hard surface; as base solvent and coupling agent of solvent-type silk-screen printing ink; as solvent and coupling agent of vat dye textile; as coupling agent and skin-care agent in cosmetic formula; as stabilizer of pesticide and coagulating?agent of floor brightener. -
Dpmâ is used as solvent for pvc stabilizer, nitrocellulose, ethyl cellulose, polyvinyl acetate, solvent for paint and dyestuff, and an ingredient of brake fluid. It can be used as solvent of printing ink, enamel paint, cutting fluid and operating oil; as coupling agent of water-based paint (usually used by mixing up); as active solvent of water-based paint; as solvent and coupling agent of household and industrial cleanser, remover for grease and paint, cleanser for metal and hard surface; as base solvent and coupling agent of solvent-type silk-screen printing ink; as solvent and coupling agent of vat dye textile; as coupling agent and skin-care agent in cosmetic formula; as stabilizer of pesticide and coagulating?agent of floor brightener. -
Intended use: Toxoplasma IGG/IGM rapid test is a rapid immunochromatographic test for the simultaneous detection of IGM and IGG antibodies to toxoplasma gondii in human serum/plasma. The test can be used as a screening test for toxoplasma infection and as an aid for differential diagnosis of the self limiting primary toxoplasma infections and the potentially fatal secondary toxoplasma infections in conjunction with other criteria. Test principle: The toxoplasma IGG/IGM rapid test is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) A burgundy colored conjugate pad containing toxoplasma recombinant envelope antigens conjugated with colloid gold (toxoplasma conjugates) and rabbit igg-gold conjugates, 2) A nitrocellulose membrane strip containing two test bands (t1 and t2 bands) and a control band (c band). The t1 band is pre-coated with the antibody for the detection of IGM anti-toxoplasma, t2 band is coated with antibody for the detection of igg anti-toxoplasma, and the c band is pre-coated with goat anti rabbit IGG. Absence of any t bands (t1 and t2) suggests a negative result. The test contains an internal control (c band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit igg/rabbit igg-gold conjugate regardless of the color development on any of the t bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Reagents and materials supplied : 1. Test cassette individually foil pouched with a desiccant. 2. Plastic dropper 3. Buffer 4. Package insert. Storage and stability: The kit must be stored at 2-30pc. Warning and precautions: 1. For in vitro diagnostic use only. Not for medicinal use. 2. Do not use beyond expiry date. 3. Read the instructions careful y before performing the test. 4. Handle all specimen as potential y infectious. 5. Follow standard biosafety guidelines for handling and disposal of potential y infective material.
Intended use: Toxoplasma igg/igm rapid test is a rapid immunochromatographic test for the simultaneous detection of igm and igg antibodies to toxoplasma gondii in human serum/plasma. The test can be used as a screening test for toxoplasma infection and as an aid for differential diagnosis of the self limiting primary toxoplasma infections and the potentially fatal secondary toxoplasma infections in conjunction with other criteria. Test principle: The toxoplasma igg/igm rapid test is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) a burgundy colored conjugate pad containing toxoplasma recombinant envelope antigens conjugated with colloid gold (toxoplasma conjugates) and rabbit igg-gold conjugates, 2) a nitrocellulose membrane strip containing two test bands (t1 and t2 bands) and a control band (c band). The t1 band is pre-coated with the antibody for the detection of igm anti-toxoplasma, t2 band is coated with antibody for the detection of igg anti-toxoplasma, and the c band is pre-coated with goat anti rabbit igg. Absence of any t bands (t1 and t2) suggests a negative result. The test contains an internal control (c band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit igg/rabbit igg-gold conjugate regardless of the color development on any of the t bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Reagents and materials supplied: 1. Test cassette individually foil pouched with a desiccant. 2. Plastic dropper 3. Buffer 4. Package insert. Storage and stability: The kit must be stored at 2-30 c. Warning and precautions: 1. For in vitro diagnostic use only. Not for medicinal use. 2. Do not use beyond expiry date. 3. Read the instructions careful y before performing the test. 4. Handle all specimen as potential y infectious. 5. Follow standard biosafety guidelines for handling and disposal of potential y infective material.
Product Name Fecal Occult Blood(FOB)Test Kit (Colloidal Gold Method) Purpose To detect the content of FOB in human fecal in vitro qualitatively.For Professional Use only. Principles of Detection The FOB Rapid Test is a one-step chromatographic sandwich immunoassay. The test consists of: 1) a conjugate pad containing HB monoclonal antibody conjugated with colloidal gold. 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HB antibody, and the C line is pre-coated with a control line antibody (goat-anti-mouse IgG antibody). After addition of the sample, FOB will bind with a colloidal gold-labeled antibody on the conjugate release pad. The resulting complex flows over the nitrocellulose membrane where a specific capture reagent is pre-coated and a red line can be seen at the test zone (T). Unreacted colloidal gold-labeled antibodies in the sample are captured at the control zone (C). The intensity and speed at which the color develops depend on the FOB concentration in the sample. Reference range This kit can detect FOB at a minimum of 50ng/ml. Performance Characteristics 1. Critical value and repeatability: 1) The quality control substance of FOB with a concentration of 50ug/mL was detected for 20 times, and the positive coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent. 2) The quality control substance of FOB with a concentration of 10ng/mL was detected for 20 times, and the negative coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent. 2. Analysis specificity: 500ug/mL bovine HB,500ug/mL pork HB,500ug/ mL chicken HB,500ug/mL goat HB,2000ug/mL Horseradish Peroxidase specific quality control substance were all negative. 3.HOOK effect: human FOB positive quality control substance of 2000ug/mL was detected and the result was positive.
This kit is only used for the in vitro qualitative detection of 2019-nCoV antigen from human nasopharyngeal swab, nasal swab or oropharyngeal swab specimens. This kit is suitable for the auxiliary diagnosis of COVID-19, the results are for clinical reference only and cannot be used as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patients should be considered in combination with their symptoms/signs, medical history, other laboratory tests and treatment responses. Positive test result needs to be further confirmed, negative result does not preclude 2019-nCoV infection. This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of in vitro diagnostic procedures. TEST PRINCIPLE The kit is immunochromatographic and uses double-antibody sandwich method to detect 2019-nCoV N protein antigen. During detection, the treated specimens are loaded into the sample wells of the test card. When the concentration of 2019-nCoV antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies first. Under chromatography, the complexes move forward along the nitrocellulose membrane till captured by pre-coated monoclonal antibody of 2019-nCoV in detection zone on nitrocellulose film (T) to form a pink/purple reaction line on the detection zone, at this point the result is positive; conversely, if there is no viral antigen or the concentration of antigen in specimen is below the minimum detection limit, no pink/purple reaction line appears in the detection zone, at this point the result is negative. Regardless of whether the sample contains viral antigens or not, a pink/purple reaction line will appear in the quality control zone (C), the pink/purple reaction line that appears in the quality control zone (C) is the criterion for determining if the chromatography process is normal.
CAS No.: As Per Item Other Names: Solvent Soluble Dyes Place of Origin: India Type Of Dye: Solvent Metal complex Dye Brand: Anhard Export Form: Powder Color :Full Range Color Appearance: Grain Heat Stability: good PH Value: 7-8 Purity: 99% Grade: Technical Solubility Gpl At Rt: 100gpl Strength Reflectance: 100% Heat Resistance: Yes Water Resistance: Yes Usage: Ink Dyestuffs, Leather Dyestuffs, Paint Dyestuffs, Plastic Dyestuffs, Textile Dyestuffs Solubility :Industrial Solvent Market: Worldwide Applications: â?¢ Solvents metal complex dyes Printing Inks (Flexographic, Stationery ink & Gravure Inks) â?¢ Solvents metal complex dyes Surface Coating (Paints, Nitrocellulose lacquers, PVC lacquers, Acid-cured finishes, Amine-cured finishes, Peroxide-cured finishes, Stoving finishes, Polyurethane finishes) â?¢ Solvents metal complex dyes Wood stains(coated with Peroxide-cured finish, Amine-cured finish, Acid-cured finish, Polyurethane finish) â?¢ Solvents metal complex dyes Coloration of anodized aluminium. â?¢ Solvents metal complex dyes for Aluminium foil printing. â?¢ Solvents metal complex dyes Coloration of Leather. â?¢ Solvents metal complex dyes Shoe polish. â?¢ Solvents metal complex dyes Plastics (Polyester resins, Cellulose nitrate, Cellulose acetate, Polymethylmehacrylate) â?¢ Solvents metal complex dyes Office Requisites (Felt-tip marking inks, Ball pen inks) Features: â?¢ Excellent Solubility â?¢ Brilliant shades â?¢ Good compatibility with most resins â?¢ Excellent acid-proof, alkali & heat resistance; â?¢ High light fastness â?¢ Absence of free heavy metals â?¢ Environment-friendly â?¢ Non-toxic â?¢ Long stability if stored properly â?¢ Colorful â?¢ Reasonable price
CAS No.: As Per Item Other Names: Solvent Soluble Dyes Place of Origin: India Type Of Dye: Solvent Metal complex Dye Brand: Anhard Export Form: Powder Color :Full Range Color Appearance: Grain Heat Stability: good PH Value: 7-8 Purity: 99% Grade: Technical Solubility Gpl At Rt: 100gpl Strength Reflectance: 100% Heat Resistance: Yes Water Resistance: Yes Usage: Ink Dyestuffs, Leather Dyestuffs, Paint Dyestuffs, Plastic Dyestuffs, Textile Dyestuffs Solubility :Industrial Solvent Market: Worldwide Applications: â?¢ Solvents metal complex dyes Printing Inks (Flexographic, Stationery ink & Gravure Inks) â?¢ Solvents metal complex dyes Surface Coating (Paints, Nitrocellulose lacquers, PVC lacquers, Acid-cured finishes, Amine-cured finishes, Peroxide-cured finishes, Stoving finishes, Polyurethane finishes) â?¢ Solvents metal complex dyes Wood stains(coated with Peroxide-cured finish, Amine-cured finish, Acid-cured finish, Polyurethane finish) â?¢ Solvents metal complex dyes Colouration of anodized aluminium. â?¢ Solvents metal complex dyes for Aluminium foil printing. â?¢ Solvents metal complex dyes Colouration of Leather. â?¢ Solvents metal complex dyes Shoe polish. â?¢ Solvents metal complex dyes Plastics (Polyester resins, Cellulose nitrate, Cellulose acetate, Polymethylmethacrylate) â?¢ Solvents metal complex dyes Office Requisites (Felt-tip marking inks, Ball pen inks) Features: â?¢ Excellent Solubility â?¢ Brilliant shades â?¢ Good compatibility with most resins â?¢ Excellent acid-proof, alkali & heat resistance; â?¢ High light fastness â?¢ Absence of free heavy metals â?¢ Environment-friendly â?¢ Non-toxic â?¢ Long stability if stored properly â?¢ Colorful â?¢ Reasonable price
Co-virion Rapid Antigen Test is an immunochromatographic test designed to qualitatively detect SARS-CoV- 2 antigen in nasopharyngeal geal swab specimens. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections. Co-virion Rapid Antigen Test is an immunochromatographic test designed to detect the nucleocapsid protein of SARS-CoV-2 in nasopharyngeal swabs (NP). The test strip contains colloidal-gold conjugated particles with monoclonal antibodies against the nu- cleo- capsid protein of SARS-CoV-2. The capture antibodies for nucleocapsid protein of SARS-CoV-2 are coated on the nitrocellulose membrane. When the sample is applied to the sample window (S well), the conjugates dried in the reagent pad are dissolved and migrate along with the sample. If SARS-CoV-2 is present in the sample, a complex formed between the anti-SARS-CoV-2 conjugate and the virus will be captured by the specific an- ti-SARS-CoV-2 monoclonal antibodies coated on the test line region (T), which develops a red line in T region. Presence of T line indicates a positive result. There is also an internal control line to check the accuracy of the test performance. The control line is coated with goat anti-Rabbit IgG antibody which binds to the gold labeled antibody. Failure to form C line confirms the incorrect procedural technique.
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human serum/plasma/ control Specimen volume : 75 Microliter stored at ; 4 - 30 DegreeC Cat No ; CFPC-44 T3 Assessing to diagnosis & to monitor thyroid diseases(T3) This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement. INTENDED USE : ichroma T3 is a fluorescence Immunoassay (FIA) for the quantitative determination of triiodothyronine (total T3) in human serum/plasma. It is useful as an aid in management and monitoring of determination of thyroid disorders. For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal. MATERIALS SUPPLIED : REF CFPC-44 Components of ichroma T3 Cartridge Box: - Cartridge 25 - Detector tube 25 - Detector diluent 2 - ID chip 1 - Instruction for Use 1
Product Details: Brand : Boditech Med Incorporated Size : 25 Test Samples : Whole blood Sample volume : 75 Microliter Cat No : CFPC-38 Storage Temperature ; 4 - 30 DegreeC HbA1c Assessing the level of glycated hemoglobin in the blood This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months. INTENDED USE ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details: Brand ; Boditech Med Incorporated Size : 25 Test Samples : Serum/Plasma Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin Storage Temperature : 4 - 30 DegreeC Cat No : CFPC-21 Progesterone Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 30 Microliter Sample : human serum / plasma / control Reaction Time ; 10 mins Cat No : CFPC-32 Ferritin Monitoring deficiency/excess of iron & inflammation Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Too little ferritin can lead to anemia, while too much to liver disease, rheumatoid arthritis, other inflammatory conditions, or hyperthyroidism. The ferritin test measures the level of ferritin in the blood. INTENDED USE : ichromaâ?¢ Ferritin is a fluorescence Immunoassay (FIA) for the quantitative determination of Ferritin in human serum/plasma. It is useful as an aid for quantifying human ferritin. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigen in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by Instrument for ichrom tests to show ferritin concentration in sample. MATERIALS SUPPLIED : REF CFPC-32 Components of ichroma Ferritin Cartridge Box: - Cartridge 25 - Detector 25 - Detector Diluent 1 - ID Chip 1 - Instruction for Use 1
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 75 Microliter Sample : human serum/plasma Reaction Time : 15mins Cat No : 13010 Luteinizing Hormone (LH) Assessing and monitoring function of pituitary gland This test helps evaluate pituitary function by quantifying luteinizing hormone in the blood, to diagnose pituitary gland disease, and to determine congenitally or acquired gonadotropin dysfunction. INTENDED USE : ichroma LH is a fluorescence Immunoassay (FIA) for the quantitative determination of Luteinizing hormone (LH) in human serum/plasma. It is useful as an aid in management and monitoring of determination of evaluating fertility issues, function of reproductive organs (ovaries or testicles), or detection of the ovulation. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show LH concentration in sample. MATERIALS SUPPLIED: REF 13010 Components of ichroma LH Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction For Use 1 Box containing Detection Buffer Tubes - Detection Buffer Tubes 25.
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples: human whole blood/serum/ plasma Specimen volume : 50 microliter stored at 4 - 30 C Cat No : CFPC-91 Total IgE Assessing to diagnose acute allergic diseases This test assesses IgE in blood to support diagnosing of acute allergic diseases. INTENDED USE : ichroma Total IgE is a fluorescence immunoassay (FIA) for the quantitative determination of total IgE in human whole blood/serum/ plasma. It is useful as an aid in diagnosis and management of allergic disease. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show total IgE concentration in the sample. MATERIALS SUPPLIED : REF CFPC-91 Components of ichroma Total IgE Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box - Detection Buffer 25
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 75 Microliter Sample : serum/plasma/control Storage Temperature : 4-30 DegreeC. Cat No : CFPC-27 Prolactin (PRL) Assessing to diagnose hypothalamic impairments & pituitary disorders This test helps select and diagnose mammary gland development, infertility treatment and pituitary diseases by quantifying blood PRL. INTENDED USE : ichroma PRL is a fluorescence Immunoassay (FIA) for the quantitative determination of Prolactin (PRL) in human serum/plasma. It is useful as an aid in management and monitoring of hypothalamic-pituitary disorders. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigenantibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PRL concentration in sample. MATERIALS SUPPLIEED : REF CFPC-27 Components of ichroma PRL Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box: - Detection Buffer tubes 25
