Lactate FS

April 29, 2024

Product Number: 1 4001

Description

Lactate is the final product of the anaerobic glycolysis and serves as an indicator of the oxygen status in cellular tissues. Increased lactate levels in the blood occur in anoxia due to shock, congestive heart failure, intoxication, and thiamine deficiency. Therefore, lactate is measured in intensive care medicine. As a metabolic variable for the capability of the muscles lactate determination is used in the evaluation of the training status in athletes.

Features

Ready to use reagent.

Proline Lactate 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 Lactate 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

Enzymatic UV test with lactate dehydrogenase (LDH)
No interference: ascorbic acid 30 mg/dL, bilirubin 60 mg/dL, hemoglobin 1000 mg/dL, lipemia to triglycerides 2000 mg/dL, dopamine 10 mg/L, L-dopamine 20 mg/L, methyldopamine 10 mg/L, and glycolic acid 1200 mg/L.
Measurement ranges from 120 mg/dL with a lower limit of detection of 1 mg/dL

Calibrator

TruCal U

Control

Kit Lines

No. Catalog	R1	R2	Kit Size
1 4001 99 88 021	5 x 20 mL	1 X 25 mL	Multi Purpose Kit
1 4001 99 88 921	4 X 18 mL	4 X 4 mL	Proline® R-910

Reference Range

Lactate serves as indicator for the oxygen status in cellular tissues; high levels occur in anoxia due to shock, congestive heart failure, intoxication and thiamine deficiency.

Plasma:
Venous	4.5 – 19.8 mg/dL	0.5 – 2.2 mmol/L
Arterial	4.5 – 14.4 mg/dL	0.5 – 1.6 mmol/L

CSF:
Adults	10 – 22 mg/dL	1.1 – 2.4 mmol/L
Newborn	10 – 60 mg/dL	1.1 – 6.7 mmol/L
3-10 Days	10 – 40 mg/dL	1.1 – 4.4 mmol/L
> 10 Days	10 – 25 mg/dL	1.1 – 2.8 mmol/L

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