Albumin FS

December 10, 2024

Product number: 1 0220

Description

Albumin is an important binding and transport protein for various substances in plasma and the main contributor to the plasma osmotic pressure. Measurement of albumin in serum is used for diagnosis and monitoring of liver diseases, e.g. liver cirrhosis. Furthermore, albumin levels indicate the health and nutritional status of an individual and, therefore, are used for detecting malnutrition and for prognosis in elderly hospitalized patients.

Increased in

Dehydration

Decreased in

Insulinoma
Adrenal cortex insufficiency
Hypopituitarism
Extra – pancreatic neoplasm
Severe liver disease
Alcohol consumption
Drugs, eg. sulfonylureas, salicylates, phenformin, insulin, etc.

Feature

Ready to use reagent.

Proline Albumin FS comes in a liquid format which provides convenience for users as no reconstitution is required which helps reduce the risk of misdiagnosis.

Open system reagent, compatible with a wide range of instruments.

Proline Albumin FS reagent is suitable for various third party analyzers such as Abbott, Advia, Cobas, Hitachi, Olympus, Response, TokyoBoeki and Beckman Coulter. Please contact our technical support at marketing@proline.co.id for further compatibility information on other types of analyzers.

Specification

Photometric test using bromocresol green.
No interference: ascorbic acid 30mg/dL, bilirubin 70mg/dL, hemoglobin 500mg/dL, and lipemia up to triglycerides 800 mg/dL
Measurement linearity up to 6 g/dL
Lower limit of detection 0.1 g/dL

Calibrator

TruCal U

Control

Kit Lines

No. Catalogue	R1	Kit Size
1 0220 99 10 022	6 X 20 mL	Multi Purpose Kit
1 0220 99 10 025	4 X 80 mL	Multi Purpose Kit
1 0220 99 10 027	4 X 62,5 mL	Multi Purpose Kit
1 0220 99 10 029	4 X 200 mL	Multi Purpose Kit
1 0220 99 10 182	4 X 60 mL	TMS50i
1 0220 99 10 192	4 X 60 mL	TMS24i
1 0220 99 10 592	4 X 60 mL	Mindray
1 0220 99 10 915	6 X 60 mL	Hitachi 917
1 0220 99 10 923	4 X 38 mL	Proline® R-910
1 0220 99 10 952	6 X 40 mL	Advia
1 0220 99 10 961	6 X 25 mL	Other Automated Instrument

Reference Range

Adult	3.5 – 5.2 g/dL	507– 756 µmol/L

Each laboratory should check whether the reference range can be calculated for its patient population and determine its own reference range if necessary.

For diagnostic purposes, outcomes should always be assessed against the patient's medical history, clinical examination, and other findings.

References

Johnson AM, Rohlfs EM, Silverman LM. Proteins. In: Burtis CA, Ashwood ER. 3rd editors. Tietz textbook of clinical chemistry. 3 ed. Philadelphia: W. B. Saunders Company; 1999. p.477-540.
Thomas L. Clinical Laboratory Diagnostics. 1 ed. Frankfurt: TH-Books Verlagsgesellschaft; 1998. p. 652-6.
Guder WG, Zawta B et al. The Quality of Diagnostic Samples. 1 ed. Darmstadt: GIT Verlag; 2001; p. 14-5.
Dati F, Schumann G, Thomas L, Aguzzi F, Baudner S, Bienvenu J et al. Consensus of a group of professional societies and diagnostic companies on guidelines for interim reference ranges for 14 proteins in serum based on the standardization against the IFCC/BCR/CAP reference material (CRM 470). Eur J Clin Chem Clin Biochem 1996;34:517-20.
Young DS. Effects of Drugs on Clinical laboratory Tests. 5th ed. Volume 1 and 2. Washington, DC: The American Association for Clinical Chemistry Press 2000.
Bakker AJ, Mücke M. Gammopathy interference in clinical chemistry assays: mechanisms, detection and prevention. ClinChemLabMed 2007;45(9):1240-1243.