Uric Acid Clinical Chemistry

Price :
Sale priceRs. 600.00

Intended Use: This reagent kit is used for in-vitro quantitative determination of uric acid in human serum, plasma or urine.
Pack size: 2 X 50 ml
Shelf life: 18 months
Storage: 2° to 8° C
Price: Up to 5 kits/ Order Rs. / Unit + 12% GST Extra

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Pack Size

Uric Acid Clinical Chemistry

2 X 50 ml

 

Uric Acid Reagents – For Accurate Quantitative Estimation in Serum or Plasma

 

Vanguard Diagnostics’ Uric Acid Reagents are designed for the quantitative determination of uric acid in human serum or plasma, using a precise enzymatic colorimetric method. This diagnostic-grade formulation enables reliable detection for routine clinical biochemistry, supported by robust reagent stability, minimal interference, and clear procedural steps aligned with international standards.

 


 

Why Choose Vanguard’s Uric Acid Reagents?

 

  • Based on Uricase-POD Methodology: A proven enzymatic reaction where uricase converts uric acid to allantoin and hydrogen peroxide, followed by a Trinder reaction to produce a measurable red chromogen.
  • High Accuracy and Linearity: Linear up to 20 mg/dL, ideal for most clinical ranges. Results remain reliable even at borderline pathophysiological concentrations.
  • Convenient Two-Reagent System: Easy-to-use reagents include phosphate buffer with enzymes, 4-aminoantipyrine, TOOS, peroxidase, and stabilisers.
  • Optimised for Manual and Automated Analysers: Protocols are compatible with semi-auto and fully automated systems used in clinical labs.

 

 


 

 

Test Parameters

 

Parameter

Details

Methodology

Enzymatic colorimetric (Uricase-POD)

Sample Type

Serum or plasma (free from haemolysis)

Wavelength

520 nm (505–550 nm acceptable)

Reaction Time

5 minutes at 37°C or 10 minutes at room temperature

Linearity

Up to 20 mg/dL

Reference Ranges

Men: 3.4 – 7.0 mg/dLWomen: 2.4 – 6.0 mg/dL

Storage Conditions

2–8°C (Do not freeze)

Pack Sizes Available

2 x 50 mL

 


 

Intended Use

 

This uric acid test reagent kit is intended for in vitro diagnostic use by qualified personnel in medical laboratories. It supports the monitoring and diagnosis of conditions such as gout, kidney dysfunction, metabolic syndrome, and chemotherapy-related uric acid imbalances.

 


 

Reagent Composition

 

  • Reagent 1 (R1): Phosphate buffer, uricase, TOOS, 4-AAP, sodium azide (preservative)
  • Reagent 2 (R2): Peroxidase, phosphate buffer, stabilisers

 

Both reagents are ready-to-use and do not require further preparation.

 


 

Procedure Overview

 

  1. Mixing: Add R1 and R2 to sample/test tubes as per volume instructions.
  2. Incubation: Maintain at 37°C for 5 minutes (or room temperature for 10 minutes).
  3. Measurement: Read absorbance at 520 nm against blank within 30 minutes.

 

Full procedural details are available in the Uric Acid IFU PDF.

 


 

Other Related Reagents You Might Find Useful

 

 


These links help complete the test panel for renal and metabolic evaluations using clinical biochemistry reagents.

 


 

FAQs

 

1. What are uric acid reagents used for?

Uric acid reagents are used to measure uric acid levels in blood samples. This helps in diagnosing and monitoring gout, renal function disorders, and conditions related to purine metabolism.


2. How should the reagents be stored?

Store at 2–8°C, away from light. Do not freeze the reagents.


3. What type of analyser can I use for this test?

The kit is compatible with both manual and automated analysers that can measure absorbance at 520 nm.


4. Can I use plasma samples?

Yes, both serum and plasma samples can be used, provided they are free from haemolysis.


5. What is the shelf life of the uric acid reagent kit?

Reagents are stable until the expiration date printed on the label, provided storage conditions are followed.

 

Shipping Policy:

- We can supply pan India to all the post codes.
- We can ship within 3 - 4 business days of receiving the payment in our bank.

 

Replacement Policy:

 Returns will be considered on account of the following conditions only.

Condition

Maximum Reporting time after receipt

Compensation

Time

Material received in broken condition

24 hrs

With evidence

Replacement FOC

Within 7 days

Material received short

24 hrs

With evidence

Replacement FOC

Within 7 days

Performance related quality problem

7 days

With test report

Replacement FOC

Within 7 days

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