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Elabscience
SKU:E-CL-H0169
Human PINP(Procollagen I N-terminal Propeptide ) CLIA Kit
Human PINP(Procollagen I N-terminal Propeptide ) CLIA Kit
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$682.00 USD
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The HUMAN PINP (Procollagen I N-Terminal Propeptide) CLIA Kit is a cutting-edge diagnostic tool designed to accurately measure the levels of Procollagen I N-Terminal Propeptide (PINP) in human serum or plasma samples. PINP is a specific marker for bone formation and is widely used in clinical research and diagnosis of bone-related disorders such as osteoporosis and osteogenesis imperfecta. This CLIA (Chemiluminescent Immunoassay) kit offers a highly sensitive and reliable method for quantifying PINP levels, providing valuable insights into bone metabolism and health.
This advanced CLIA kit utilizes a sandwich immunoassay principle, where two highly specific monoclonal antibodies are employed to capture and detect the PINP analyte. The assay is performed in a 96-well microplate format, allowing for simultaneous analysis of multiple samples. The kit includes all necessary reagents and controls, ensuring accurate and reproducible results. With a wide dynamic range and excellent sensitivity, this kit can detect PINP levels as low as 0.1 ng/mL, enabling precise quantification even in samples with low analyte concentrations.
The HUMAN PINP CLIA Kit is user-friendly and time-efficient, with a total assay time of only 2.5 hours. The procedure involves simple steps, including sample preparation, incubation, washing, and chemiluminescent detection. The kit provides detailed instructions, guiding users through each step to ensure optimal performance. The results are obtained through a luminometer, and the data can be easily analyzed using standard software. With its high accuracy, precision, and reproducibility, this CLIA kit is an indispensable tool for researchers and clinicians involved in bone-related studies and diagnostics.
In summary, the HUMAN PINP CLIA Kit is a state-of-the-art diagnostic tool that offers a reliable and sensitive method for measuring Procollagen I N-Terminal Propeptide levels in human serum or plasma samples. With its advanced sandwich immunoassay principle, wide dynamic range, and user-friendly design, this kit provides valuable insights into bone metabolism and health. Whether used in research or clinical settings, this CLIA kit is an essential resource for studying bone-related disorders and monitoring treatment efficacy.
This advanced CLIA kit utilizes a sandwich immunoassay principle, where two highly specific monoclonal antibodies are employed to capture and detect the PINP analyte. The assay is performed in a 96-well microplate format, allowing for simultaneous analysis of multiple samples. The kit includes all necessary reagents and controls, ensuring accurate and reproducible results. With a wide dynamic range and excellent sensitivity, this kit can detect PINP levels as low as 0.1 ng/mL, enabling precise quantification even in samples with low analyte concentrations.
The HUMAN PINP CLIA Kit is user-friendly and time-efficient, with a total assay time of only 2.5 hours. The procedure involves simple steps, including sample preparation, incubation, washing, and chemiluminescent detection. The kit provides detailed instructions, guiding users through each step to ensure optimal performance. The results are obtained through a luminometer, and the data can be easily analyzed using standard software. With its high accuracy, precision, and reproducibility, this CLIA kit is an indispensable tool for researchers and clinicians involved in bone-related studies and diagnostics.
In summary, the HUMAN PINP CLIA Kit is a state-of-the-art diagnostic tool that offers a reliable and sensitive method for measuring Procollagen I N-Terminal Propeptide levels in human serum or plasma samples. With its advanced sandwich immunoassay principle, wide dynamic range, and user-friendly design, this kit provides valuable insights into bone metabolism and health. Whether used in research or clinical settings, this CLIA kit is an essential resource for studying bone-related disorders and monitoring treatment efficacy.
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