Immunoassays Reagents

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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.

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Diagnosis of endocrine dysfunction and adrenal disease This test measures the cortisol level in the blood. One can use the whole blood for ease of sample pretreatment. The test takes 10 minutes, and the result could provide information about adrenal diseases and endocrine dysfunction.

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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.

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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.

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With the kidney not functioning properly, the cystatin level increases. With this test, the clinician can find GFR (Glomerular Filtration Rate). The Cystatin C test measures the level of cystatin C in the blood with the serum/plasma in 10 minutes.

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This is a screening test that quantifies microalbumin from the first urine in the morning or random concentrated urine to check the extent of kidney damage and predict the progression to kidney failure. Continuous measurement of microalbumin concentration can help patients receive appropriate treatment and confirm treatment effects.

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Follicle-stimulating Hormone (FSH) Diagnosis of early menopause & ovarian degeneration and infertility This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.

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Starter reagent kit required to generate the chemiluminometric light signal necessary for the performance of MAGLUMI assays on the Maglumi fully auto analyzer (Including Maglumi 1000, Maglumi 2000, Maglumi 2000 plus).

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The TSH test is often the test of choice for evaluating thyroid function and/or symptoms of hyperthyroidism or hypothyroidism. It is frequently ordered along with or preceding a T4 test. Other thyroid tests that may be ordered include a T3 test and thyroid antibodies (if autoimmune-related thyroid disease is suspected). TSH testing is used to: Diagnose a thyroid disorder in a person with symptoms; Screen newborns for an underactive thyroid; Monitor thyroid replacement therapy in people with hypothyroidism Diagnose and monitor female infertility problems; Help evaluate the function of the pituitary gland (occasionally); Screen adults for thyroid disorders, although expert opinions vary on who can benefit from screening and at what age to begin; The doctor may order a TSH test when someone has symptoms of hyperthyroidism or hypothyroidism and/or when a person has an enlarged thyroid gland.

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Vitamin B12, also called cobalamin, is a water-soluble vitamin. Cobalamin can be found in animal products such as meat, eggs, milk and other dairy products. During the intake process, cobalamin conjugates with a factor known as the combining binding-protein in the stomach, then absorbed by the ileum. Intrinsic factor is necessary for absorption process, once getting into the circulation; the cobalamin is stored in the liver. When being required, the cobalamin will be released into the plasma by the VB12 binding protein. VB12 is normally involved in the metabolism of every cell of the body, especially affecting the DNA synthesis and regulation but also fatty acid synthesis and energy production. However, many (though not all) of the effects of functions of VB12 can be replaced by sufficient quantities of folic acid (vitamin B9), since VB12 is used to regenerate folate in the body. Most VB12 deficiency symptoms are actually folate deficiency symptoms, since they include all the effects of pernicious anemia and megaloblastosis, which are due to poor synthesis of DNA when the body does not have a proper supply of folic acid for the production of thymine. The lack of VB12 can be caused by a variety of reasons. The most common reason is a lack of intrinsic factor, resulting in that VB12 cannot be absorbed from food. This condition is called anemia, mostly affecting people over the age of 50 years. The gastric resection is another reason of VB12 deficiency, after surgery or malabsorption caused by various bacteria or inflammatory disease affecting the small intestine. VB12 uptake has a positive correlation with the functional length of small intestine. The lack of VB12 is rarely caused by abnormal dietary, unless no animal food is consumed in years.

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1. Intended Use Modules required for the performance of the MAGLUMI assays on the Maglumi fully auto analyzer (Including Maglumi 1000, Maglumi 2000, Maglumi 2000 plus).

2. Material provided 6×64 reaction modules for 2304 tests. 6×64 MAGLUMI modules with 6 cavities each. For additional details such as proper test performance of MAGLUMI® 2000 assays consult instructions for use of the assay to be performed.

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Total T4 and free T4 are two separate tests that can help a doctor evaluate thyroid function. The total T4 test has been used for many years to help diagnose hyperthyroidism and hypothyroidism. It is a useful test but can be affected by the amount of protein available in the blood to bind to the hormone. The free T4 test is a newer test that is not affected by protein levels. Since free T4 is the active form of thyroxine, the free T4 test is thought by many to be a more accurate reflection of thyroid hormone function and, in most cases, its use has replaced that of the total T4 test. Whichever thyroxine measurement is ordered, it is usually ordered along with or following a TSH test. This helps the doctor to determine whether the thyroid hormone feedback system is functioning as it should, and the results of the tests help to distinguish between different causes of hyperthyroidism and hypothyroidism. Sometimes a T3 test will also be ordered to give the doctor additional diagnostic information. A T4 and TSH test may be ordered to help evaluate a person with a goiter and to aid in the diagnosis of female infertility. If a doctor suspects that someone may have an autoimmune-related thyroid condition, then thyroid antibodies may be ordered along with a T4 test. In those with known thyroid dysfunction, T4 and/or TSH tests may be ordered to monitor thyroid function. Newborns are commonly screened for T4 levels as well as TSH concentrations to check for congenital hypothyroidism, which can cause mental retardation if left untreated. A total T4 or free T4 test is primarily ordered in response to an abnormal TSH test result. Sometimes the T4 will be ordered along with a TSH to give the doctor a more complete evaluation of the adequacy of the thyroid hormone feedback system. These tests are usually ordered when a person has symptoms of hyperthyroidism or hypothyroidism. Signs and symptoms of hyperthyroidism may include: Increased heart rate; Anxiety; Weight loss; Difficulty sleeping; Tremors in the hands; Weakness; Diarrhea (sometimes); Light sensitivity, visual disturbances. The eyes may be affected: puffiness around the eyes, dryness, irritation, and, in some cases, bulging of the eyes. Symptoms of hypothyroidism may include: Weight gain, Dry skin, Constipation, Cold intolerance, Puffy skin, Hair loss, Fatigue, Menstrual irregularity in women. Severe untreated hypothyroidism, called myxedema, can lead to heart failure, seizures, and coma. In children, hypothyroidism can stunt growth and delay sexual development. Sometimes they are ordered as screening tests during routine blood testing, but expert opinions vary on who can benefit from screening and at what age to begin. In those with known thyroid disorders, the TSH and sometimes T4 are ordered at intervals to monitor the effectiveness of treatment. In pregnant women with thyroid disorders, the doctor is likely to order thyroid testing early and late in the pregnancy and for a time period following delivery to monitor the mother and baby. Thyroid hormone screening is commonly performed on newborns as part of newborn screening programs

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The adenovirus causes upper respiratory diseases. It is highly contagious, leading to various complications such as pneumonia and conjunctivitis. They display symptoms similar to those from Kawasaki disease and bacterial infections. The exact identification of the cause is of critical clinical importance. Adeno tests identify the adenovirus in a fast and easy-to-use step.

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With Dengue NS1 Ag, one can diagnose Dengue virus infection early and provide means of prognosis monitoring Dengue fever is an acute febrile disease caused by the dengue virus, mainly transmitted by mosquitoes. Reinfection is not uncommon and can grow into severe dengue fever. Dengue NS1 Ag can help with the diagnosis of dengue infection at an early stage, which should help with treatment planning and prognosis monitoring.

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ASO is an antigen against the toxin produced by the streptococci. The presence of these antibodies indicates an exposure to these bacteria. The ASO test can detect GAS (group A streptococcus) infection with a blood sample.

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• New PCR assay for SARS-CoV-2, Flu and RSV identification from a single respiratory sample
• Specimen type: nasopharyngeal swabs, oropharyngeal swabs and nasopharyngeal/nasal wash
• High sensitivity and specificity
• Results around 1.5 hours after extraction
• An endogenous internal standard detection system, to avoid false negative result
• Opening reagent kit available for Universal Real time PCR analyzer

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Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma™ & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock.

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Use an anti-PRL monoclonal antibody to label ABEI, and use another monoclonal antibody to Nano Magnetic Microbeads. Sample, Calibrator or Control with ABEI Label, and magnetic microbeads are mixed thoroughly and incubated at 37℃, forming a sandwich; after sediment in a magnetic field, decant the supernatant, then cycle washing for 1 time. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of PRL present in samples.

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The Finecare™ PCT Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Procalcitonin (PCT) in human whole blood, serum or plasma. This test is used as an aid to diagnosis severe, bacterial infection and sepsis.STORAGE AND STABILITY1. Store the test kit at 4℃~30℃ up to the expiration date printed on package.2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing.3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

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hsCRP Quantitative Rapid TesthsCRP is a sensitive index to distinguish the low level inflammatory state, which can be used as an auxiliary means for risk identification of cardiovascular disease. The serum CRP level is closely related to the occurrence, severity and prognosis of cardio-cerebrovascular diseases such as atherosclerosis (AS) and acute cerebral infarction (ACI). In conjunction with the traditional clinical diagnosis of acute coronary syndrome, it can be used as an early warning indicator for the recurrence of coronary artery disease or acute coronary syndrome.

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INTENDED USEThe kit has been designed for the quantitative determination of free β-chains of human chorionic gonadotropin (free β-HCG) in human serum. The method can be used for samples over the range of 1.1-200 ng/ml. The test has to be performed on the Fully-auto chemiluminescence immunoassay (CLIA) analyzer MAGLUMI (Including Maglumi 600,Maglumi 1000,Maglumi 1000 Plus, Maglumi 2000,Maglumi 2000 Plus,Maglumi 3000 and Maglumi 4000).

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Use an anti-T3 monoclonal antibody to label ABEI, and use a purified T3 antigen to label Nano Magnetic Microbeads. Sample, Calibrator, or Control ,ABEI Label, and Buffer are mixed thoroughly and incubated at 37℃, Then add Nano Magnetic Microbeads and incubated, the Sample and Nano Magnetic Microbeads competitively binding the ABEI Label, forming a immuno-complex ,after sediment in a magnetic field, decant the supernatant, then cycle washing for 1 time. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of T3 present in samples. 

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Use an anti-LH monoclonal antibody to label ABEI, and use another monoclonal antibody to coat magnetic microbeads. Sample, Calibrator or Control, with ABEI Label and magnetic microbeads are mixed thoroughly and incubated at 37℃, forming a sandwich; After sediment in a magnetic field, suck the supernatant and then cycle wash it for 1 time.Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of LH present in samples.

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Use an anti-T4 monoclonal antibody to label ABEI, and use a purified T4 antigen to coat Nano Magnetic Microbeads. Sample, Calibrator, or Control ,Buffer, mixed thoroughly with ABEI Label, and Nano Magnetic Microbeads and incubated at 37℃, then the Sample and Nano Magnetic Microbeads competitively binding the ABEI Label, forming a immuno-complex, after sediment in a magnetic field, decant the supernatant, then cycle washing for 1 time. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of FT4 present in samples. 

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Mouse anti-human IgG is used to label ABEI, and use purified Rubella antigen to coat nano magnetic microbeads. Sample, Calibrator or Control with Buffer（goat Anti-human IgM, goat Anti-human IgA） and nano magnetic microbeads coated with Rubella antigen are mixed thoroughly and incubated at 37℃ and cycle washing for 1 time. Then add ABEI Label, incubation and form a sandwich, then washing for the 2nd time. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of Rubella IgG present in samples

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PRINCIPLE OF THE TEST Competitive immunoluminometric assay: Use a purified 25-OH Vitamin D antigen to label ABEI, and use 25-OH Vitamin D monoclonal antibody to label FITC. Sample, Calibrator or Control with Displacing reagent, FITC Label and magnetic microbeads coated with anti-FITC are mixed thoroughly and incubated at 37℃, forming antibody-antigen complexes; After sediment in a magnetic field, decant the supernatant, then cycle washing for 1 time. Then add ABEI Label, incubation and washing for the 2nd time, sample antigen and ABEI labeled antigen compete to combine with FITC labeled monoclonal antibody, forming antibody-antigen complexes. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of 25-OH Vitamin D present in controls or samples.

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The TRUSTline HCV Ab Rapid Test provides fast, accurate results allowing users to detect infection during initial stages and take early steps to prevent serious complications and transmission.

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STANDARD F Dengue IgM/IgG FIA qualitatively analyzes Dengue virus specific IgM and IgG antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

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TSH ELISA Kit is a solid phase enzyme linked immunosorbent assay for the quantitative determination of the levels of Thyroid Stimulating Hormone (TSH) in human serum.

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This product performs qualitative analysis on NS1 antigen of Dengue virus in serum, plasma and whole blood.

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STANDARD F Chikungunya IgM/IgG FIA qualitatively analyzes Chikungunya virus specific IgM and IgG antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

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STANDARD F TSH FIA is a fluorescent immunoassay for the quantitative measurement of Thyroid Stimulating Hormone level in human serum. This test is to help diagnose thyroid disorder; to monitor treatment of hypothyroidism and hyperthyroidism.

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STANDARD F LH FIA is a fluorescent immunoassay for the quantitative measurement of LH level in human serum, plasma and whole blood. This test is performed to help evaluate fertility issues, function of reproductive organs (ovaries or testicles), or to detect the ovulation.

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STANDARD F hs-CRP FIA performs quantitative measurement of high-sensitivity C-Reactive Protein (hs-CRP) in serum, plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F LH FIA is a fluorescent immunoassay for the quantitative measurement of LH level in human serum, plasma and whole blood. This test is performed to help evaluate fertility issues, function of reproductive organs (ovaries or testicles), or to detect the ovulation.

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STANDARD F β-hCG FIA is a fluorescent immunoassay for the quantitative measurement of β-hCG level in human serum and whole blood. This test is performed to help diagnose pregnancy if a women is to undergo a medical treatment, be placed on certain drugs, or have other testing, such as x-rays, that might harm the developing baby

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STANDARD F TnI FIA performs quantitative measurement of Troponin I (TnI) level in plasma and whole blood specimens using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F NT-proBNP FIA is a quantitative test for the determination of the N-terminal pro brain-type natriuretic peptide (NT-proBNP) level in human serum and whole blood(EDTA).

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STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F U-Albumin FIA is a test for the quantitative measurement of microalbumin in human urine. This test is to aid to the prediction of diabetic nephropathy and cardiovascular diseases (CVD).

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STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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SD F200 tsh test kit:-STANDARD F TSH-II FIA is a quantitative test for the determination of the thyroid stimulating hormone (TSH) level in human serum and whole blood(EDTA).

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Mouse anti-human IgG is used to label ABEI, and use purified Toxo antigen to coat nano magnetic microbeads. Sample, Calibrator or Control with Buffer （goat Anti-human IgM, goat Anti-human IgA） and nano magnetic microbeads coated with Toxo antigen are mixed thoroughly and incubated at 37℃ and cycle washing for 1 time. Then add ABEI Label, incubation and form a sandwich, then washing for the 2nd time. Subsequently, the starter reagents are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of Toxo IgG present in samples.

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SD F200 tsh test kit:-STANDARD F TSH-II FIA is a quantitative test for the determination of the thyroid stimulating hormone (TSH) level in human serum and whole blood(EDTA).

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The Finecare™ AMH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of AMH in human whole blood, serum or plasma. The test is mainly used in the assessment of the ovarian reserve and as an aid in the diagnosis of polycystic ovary syndrome (PCOS).

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Human Chorionic Gonadotropin (β-hCG) Distinguish pregnancy and abnormal pregnancy The β-hCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome.

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One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH).

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Use CMV IgG value as a kind of auxiliary material for other testing data when in diagnosis. Assay results should be utilized in conjunction with other clinical and laboratory data to assist the clinician in making individual patient management decisions. A skillful technique and strict adherence to the instructions are necessary to obtain reliable results. Bacterial contamination of samples or repeated freeze-thaw cycles may affect the test results. Assay results should be utilized in conjunction with other clinical and laboratory data to assist the clinician in making individual patient management decisions. 

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TSH ELISA MERIL is used in semi auto elia reader to determine TSH level in the body

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Assessing to diagnosis & to monitor thyroid diseases(T3)

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Toxoplasmosis is a quite widespread infectious disease caused by an intracellular protozoan parasite, called Toxoplasma gondii. The disease, affecting both man and warm-blooded animals, can be transmitted by ingestion of food infected or contaminated by oocysts; direct contagion from domestic animals; or transplacental infection. Transmission of Toxoplasma through blood transfusions or organ transplantation has also been reported in the literature. In the normal adult population, toxoplasmosis has a generally benign course, being largely asymptomatic; sometimes mildly symptomatic (headache, sore throat, asthenia); or in rare cases accompanied by lymphadenitis. Exceptionally, severer disorders may be present, like myocarditis, hepatitis, pneumonia, meningoencephalitis and retinochoroiditis. The prevalence of positive serological tests increases with age, indicating past exposure. Cell-mediated immunity is generally involved in protecting from parasite infection. As a consequence, a symptomatic course is generally more frequent in patients undergoing immune -suppressive therapy, either to prevent organ rejection or as an anti-tumor therapy. Toxoplasmic encephalitis has proved to be a significant cause of death in patients with acquired immuno -deficiency syndrome.

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Use an anti-FSH monoclonal antibody to label ABEI and use another monoclonal antibody to coat magnetic microbeads. Sample, Calibrator or Control with ABEI Label, and magnetic microbeads are mixed thoroughly and incubated at 37℃, forming a sandwich; After sediment in a magnetic field, suck the supernatant and then cycle wash it for 1 time. Subsequently, Starter 1+2 substrates are added and a flash chemiluminescent reaction is initiated. The light signal is measured by a photomultiplier as RLU within 3 seconds and is proportional to the concentration of FSH present in samples.

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STANDARD F Strep A Ag FIA performs qualitative analysis by detecting Group A streptococcal antigens in samples using fluorescence immunochromatography. This product’s performance is much higher than that of other products that use the existing Gold conjugate; through STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F Adeno Respi FIA test (Analyzer+Test device) is a rapid diagnostic test that can use commercially. It has high accuracy, and provides the test result in 15 minutes with the STANDARD F analyzer.

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STANDARD F Adeno Respi FIA test (Analyzer+Test device) is a rapid diagnostic test that can use commercially. It has high accuracy, and provides the test result in 15 minutes with the STANDARD F analyzer.

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STANDARD F TB-Feron FIA (IFN-gamma) aids to diagnosis of Tuberculosis infection. TB Antigens coated in TB-Feron Tube stimulate T cells in heparinized whole blood from patients with symptoms of Tuberculosis (TB), and T cells secrete interferon-γ (IFN-γ). The concentration of IFN-γ is measured by fluorescent immunoassay (FIA) to identify in vitro responses to those recombinant TB Antigens that are associated with M.tuberculosis infection.

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STANDARD F S. pneumoniae Ag FIA test system (Analyzer + Test Device) finds S.pneumoniae antigen in urine if patients have pneumonia, and in cerebral spinal fluid sample if patients have meningitis.

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STANDARD F Legionella Ag FIA test system (Analyzer + Test device) detects Legionella pneumophila serogroup 1, 3, 5, 6 and 8 antigens via urine sample. Without any further sample processing, STANDARD F Legionella Ag FIA performs highly sensitively, and the test is not affected by Rheumatoid factor.

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STANDARD F TB-Feron FIA (IFN-gamma) aids to diagnosis of Tuberculosis infection. TB Antigens coated in TB-Feron Tube stimulate T cells in heparinized whole blood from patients with symptoms of Tuberculosis (TB), and T cells secrete interferon-γ (IFN-γ). The concentration of IFN-γ is measured by fluorescent immunoassay (FIA) to identify in vitro responses to those recombinant TB Antigens that are associated with M.tuberculosis infection.

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STANDARD F TB-Feron FIA (IFN-gamma) aids to diagnosis of Tuberculosis infection. TB Antigens coated in TB-Feron Tube stimulate T cells in heparinized whole blood from patients with symptoms of Tuberculosis (TB), and T cells secrete interferon-γ (IFN-γ). The concentration of IFN-γ is measured by fluorescent immunoassay (FIA) to identify in vitro responses to those recombinant TB Antigens that are associated with M.tuberculosis infection.

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Scrub typhus is a disease caused by Orientia tsutsugamushi that is spread through chiggers (larval mites). STANDARD F Tsutsugamushi IgM/IgG FIA is a fluorescent immunoassay for the detection of O. tsutsugamushi bacteria specific IgM and IgG antibodies in human whole blood, serum, and plasma samples.

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STANDARD F Zika IgM FIA qualitatively analyzes Zika virus specific IgM antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

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STANDARD F Zika Ag qualitatively analyzes Zika virus antigen in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

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STANDARD F HBsAg FIA is a fl uorescent immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) present in whole blood, serum and plasma.

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STANDARD F HCV Ab qualitatively analyzes antibodies specific to hepatitis C virus in serum, plasma and whole blood using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 5 minutes with its high sensitivity and specificity.

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STANDARD F C. difficile Toxin A/B FIA qualitatively analyzes Clostridium difficile Toxin A/B in human stool specimen using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.

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STANDARD F Anti-HBs FIA is a fluorescent immunoassay for the qualitative detection of antibodies directed against Hepatitis B surface antigen (HBsAg) present in patients’ whole blood, serum, and plasma.

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STANDARD F Rota/Adeno Ag FIA is a fluorescent immunoassay for the qualitative detection of the presence of Rotavirus and/or Adenovirus antigens in fecal specimens. STANDARD F Rota/Adeno Ag FIA should be used with STANDARD F Analyzers manufactured by SD BIOSENSOR.

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STANDARD F H. pylori Ag FIA is a fluorescent immunoassay for the detection of H.pylori antigen in human fecal specimens.

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STANDARD F C. difficile GDH FIA qualitatively analyzes Clostridium difficile Glutamate Dehydrogenase (GDH) antigen in human stool specimen using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.

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STANDARD F Norovirus Ag FIA is a fluorescent immunoassay for the detection of Norovirus antigen in human fecal sample. The test kit is for in vitro use only.

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STANDARD F PSA FIA performs quantitative measurement of prostate-specific antigen (PSA) level in serum, plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.

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STANDARD F iFOB FIA is a fluorescent immunoassay for the quantitative measurement of hemoglobin in fecal sample. This test is offered as a screening test for the early detection of bowel cancer in patients without symptoms.

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STANDARD F TSH-II FIA is a quantitative test for the determination of the thyroid stimulating hormone (TSH) level in human serum and whole blood(EDTA).

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STANDARD F HAV IgM qualitatively analyzes hepatitis A virus IgM antibody in serum, plasma and whole blood using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.

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STANDARD F HIV Ag/Ab FIA is a 4th generation HIV diagnostic kit, which simultaneously analyzes HIV antigen (p24) and HIV-1/2 antibodies in serum, plasma and whole blood using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.

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Covi-FERON FIA (IFN-gamma) is a fluorescence immunoassay for detecting cell-mediated immune responses to SARS-CoV-2 specifi c proteins in heparinized whole blood. Plasma from the stimulated samples in Covi-FERON tubes can be used for detection of IFN-gamma (IFN-γ) using Covi-FERON FIA (IFN-gamma) . Covi-FERON FIA (IFN-gamma) and Covi-FERON Tubes are for Research Use Only and not for diagnostic use.

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Anti Mullerian Hormone (AMH) Gen II Assay During embryonic development in males, secretion of AMH from testicular Sertoli cells is essential for the regression of the Müllerian ducts, and thus the normal development of the male reproductive tract. AMH levels drop following puberty, decreasing to a relatively low post-puberty value. During postnatal life,where serum AMH is significantly lower in females. Mean serum AMH levels increase during late puberty in women and then progressively decline to undetectable levels at menopause.

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Your thyroid gland is situated in the neck just below the Adam’s apple. The thyroid creates proteins and controls how your body uses energy and your body’s sensitivity to other hormones. Your thyroid produces triiodothyronine, a hormone known as T3. T3, along with T4 (which is also produced in the thyroid), regulates your body’s temperature, metabolism, and heart rate.

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We are engaged in offering Raj Elisa Kits to our clients. Our range of all products is widely appreciated by our clients.

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Vitamin B-12 Elisa Kit Biodetect, USA

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We are engaged in offering Psa Elisa - Kit to our clients. Our range of all products is widely appreciated by our clients.

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CA-125 Elisa - Kit Biodetect, USA

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We are engaged in offering Psa Elisa - Kit to our clients. Our range of all products is widely appreciated by our clients.

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CA-125 Elisa - Kit Biodetect, USA

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We are offering Iohexol molecule non – ionic contrast for CT with brand name of Microhex. Available in packaging of 300mg in 50 ml the range is acknowledged for the following Indications:

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Assessing to diagnose acute inflammatory and sepsis The IL-6 level is elevated with infection, sepsis, and septicemia. The IL-6 test helps evaluate patients with suspected localized infection.