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Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism

    Buy cheap Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism from wholesalers
     
    Buy cheap Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism from wholesalers
    • Buy cheap Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism from wholesalers
    • Buy cheap Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism from wholesalers

    Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism

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    Brand Name : Zecen
    Model Number : CLIA PINP
    Certification : CE, ISO13485
    Price :
    Payment Terms : L/C, D/A, D/P, T/T, Western Union, MoneyGram
    Supply Ability : 5000 Set/Sets per Month
    Delivery Time : 15 workdays
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    Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism

    Procollagen I of Aminoterminal Propeptide(PINP)for Automatic immunoassay analyzer in Bone Metabolism


    Test itemPINP
    Specification100 Test/Box for CIA series
    24 Test/Box for POCT
    Principle
    • sandwich method

    ComponentMagnetic Beads
    Calibrator Low
    Calibrator High
    PINP Anti
    Control 1
    Control 2
    Accessories Required But Not ProvidedSubstrate
    Washing solution
    Sample materialserum
    Sample volumeMore than 200μL
    Storage2-8℃



    Bone type I collagen is the most abundant form of collagen in the body, comprising approximately 90% of bone mass.


    Type I collagen is mainly synthesized in bone tissue. Procollagen is synthesized first. There is an extension peptide at the amino N-terminus and C-terminus of type I procollagen, which are respectively called Type I procollagen N-terminal propeptide (PINP). and type I procollagen C-terminal propeptide (PICP); when type I procollagen is secreted out of the cell by osteoblasts, the N-terminal and C-terminal extended peptides are cleaved by proteases, and in addition to a small amount deposited in the bone matrix, a large amount of It enters the blood circulation and is eventually metabolized and eliminated by the liver. Therefore, under the exclusion of liver disease, the detection of PINP content in blood can accurately reflect the activity of osteoblasts, which in turn reflects the intensity of bone metabolism in the body, and guides the diagnosis and treatment of diseases caused by abnormal bone metabolism.


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