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Product Name | MenoCheck picoAMH ELISA |
Description | The MenoCheck® picoAMH ELISA is FDA cleared for in vitro diagnostic use as an aid in the determination of menopausal status in women between 42 and 62 years of age. This is the only AMH test with the sensitivity to quantify declining AMH concentrations in women who are entering their menopausal transition. For more information about the test itself, please visit www.MenoCheck.com. To learn more about the utility, please reference the IFU in the documents section and the press release titled, "Ansh Labs Earns De Novo FDA Clearance for the MenoCheck® picoAMH ELISA" Wide dynamic range of 6, 7.6-1091 pg/mL with a sensitivity of 1.3 pg/mL. Requires 100 µL of Serum. Total 4.5 hours incubation at room temperature. Species reactivity includes Human, Non-Human Primate. Includes all reagents needed to run a 96-well plate, shipped at ambient temperatures and stored at 2-8C. For Research Use Only within the United States. Ansh Labs, located just south of Houston Texas, is an FDA registered manufacturer of diagnostic test kits, antibodies, antigens, and proteins. |
Size | 96-well (12x8 removable strips) microtiter plate ELISA |
Concentration | n/a |
Applications | n/a |
Other Names | Kit, EIA, assay, enzyme immunoassay, test, ELISA, biomarker |
Gene, Accession, CAS # | n/a |
Catalog # | AL-124 |
Price | please inquire |
Order / More Info | MenoCheck picoAMH ELISA from ANSH LABS |
Product Specific References | n/a |