Healgen Scientific, LLC. products

An all-in-one urine-based test that can be utilized in practically any drug screening scenario. Our drug test cups can offer panel sizes up to 14 analytes with an additional 6 adulteration.

The CK-MB Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative, lateral flow membrane based immunoassay for the detection of CK-MB in whole blood, serum or plasma. The membrane is pre-coated with capture reagent on the test line region of the test. During testing, the whole blood, serum or plasma specimen reacts with the particle coated with anti-CK-MB antibodies. The mixture migrates upward on the membrane chromatographically by capillary action to react with capture reagent on the membrane and generate a colored line. The presence of this colored line in the test line region indicated a positive result, while its absence indicated a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

The Alpha-Fetoprotein (AFP) Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of AFP in whole blood, serum or plasma to aid in the diagnosis of Hepatocellular Carcinoma or fetal open neural tube defects. Alpha-Fetoprotein (AFP) is normally produced during fetal and neonatal development by the liver, yolk sac and in small concentrations by the gastrointestinal tract. By the second year of life, AFP concentrations decrease rapidly, and thereafter only trace amounts are normally detected in serum. In general, normal adults have serum AFP concentrations of less than 10 ng/mL. Elevated AFP levels occur in several malignant diseases including hepatocellular carcinoma, testicular nonseminomatous origin, and occasionally of other entodermal origin. AFP has also been used to detect early tumors in people at high risk for liver cancer. 

The CEA Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of CEA in whole blood, serum or plasma. It is intended as an aid in the assessment and diagnosis of colorectal cancer and other types of cancer, such as pancreatic, stomach, breast, lung and certain types of thyroid and ovarian cancer. The CEA rapid test device utilizes a combination of colloidal gold conjugate and monoclonal antibodies to selectively detect elevated levels of CEA. CEA is present in high concentrations during fetal development, but ceases after birth. Therefore, it is not usually present in the blood of healthy adults. The normal CEA range for a non-smoking adult is less than 2.5 ng/mL and less than 5.0 ng/mL in a smoker.

The Adenovirus Rapid Test (Feces) is a rapid visual immunoassay for the qualitative presumptive detection of adenovirus in human fecal specimens. This kit is intended to be used as an aid in the diagnosis of adenovirus infection.

The EV71 IgM Rapid Test Cassette is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of IgM-class antibodies to human Enterovirus 71 (EV71) in human whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with EV71.

The fetal fibronectin (fFN) rapid test is a visually interpreted, qualitative immunochromatographic test device for detection of fFN in vaginal secretions during pregnancy, which is a special protein that literally holds your baby in place in the womb. The test is intended for professional use to help diagnose the rupture of fetal membranes (ROM) in pregnant women.

The FSH Menopause Rapid Test is a rapid lateral flow chromatographic immunoassay for the qualitative detection of Follicle-Stimulating Hormone (FSH) at the sensitivity of 25 mIU/mL in urine to evaluate the onset of menopause in women. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH. At the level of claimed sensitivity, the FSH menopause test shows no cross-reactivity interference from the structurally related glycoprotein hormones hCG, hLH and hTSH at high physiological levels.

The hCG One Step Pregnancy Test (Urine) is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine to aid in the early detection of pregnancy.