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BCG Albumin

BCG Albumin

SKU: R3330000005

Product for use in the quantitative determination in vitro of the Albumin concentration in human serum or plasma. The results of the test must always be interpreted in conjunction with the clinical picture.

  • Tests per Kit

    200

  • Test Category

    General Proteins

  • Target Analytes

    Albumin

  • Sample Type

    Serum or plasma

  • Kit Components

    Reagent: 3 x 14 mL,
    Ready to use

  • Tech Docs

    Instructions for Use  |  Safety Data Sheet

  • Intended Use

    For professional use only.

  • Clinical Significance

    Albumin is the plasma protein which is present in the largest quantities, constituting about half the total amount of proteins. It is synthesised in the hepatic parenchymal cells. The rate of synthesis is regulated primarily by COP (colloid osmotic pressure) and secondly, by the supply of protein. The normal half-life of albumin in plasma is 15-19 days. Increased albumin levels are present only in cases of acute dehydration. Decreased albumin levels are seen in numerous clinical conditions such as: analbuminemia, hepatopathic inflammation, loss in the urine, oedema and ascites. Rodkey in 1965 (1) and Hernandez in 1967 (2) described methods for the determination of albumin using Bromocresol Green (BCG). In 1972 Doumas (3) proposed a modified BCG method, establishing a reaction pH of 3.8. The method is based on Doumas’s study, with a further modification to improve the linearity and stability of the final reaction colour.

  • Test Principle

    In a suitable buffer solution, serum or plasma albumin binds to Bromocresol Green (BCG). The intensity of the colour which develops is directly proportional to the amount of albumin present in the sample. The presence of a tensioactive agent in the reagent increases the linearity of the reaction.

  • Stability & Storage

    Store at 15-25°C; protect from direct light. When correctly stored, the reagent is stable up to the expiry date reported on the label. A slight variation in the composition of the components may occur between batches, but this has no effect on the test results. After opening, the vial R1 and R2 are stable 30 days if recapped immediately and protected from contamination, evaporation, direct light and stored at correct temperature.

  • Required but Not Supplied

    Multicalibrator (R0300000006)
    Normal control serum (R0400000006)
    Pathological control serum (R0400000106)

Clinical Area
Method
Product Type
Packaging Unit
Compatible System
Regulatory Status

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