GENLISA™ Brucellosis Bengal Rose Plate Agglutination Antigen Kit

SKU: KAD6001 Category:

₹8,000.00

Rapid Chromatography Assay for the qualitative screening of Brucellosis Bengal Rose Plate Agglutination Antigen Kit in Serum, Plasma


Availability: 3 – 4 Weeks | Pack Size: 15 ml / 450 tests

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Description

Assay Features include:
– Ready to use protocol with for ease of use
– Strong, visible Control Lines for easy visual read
– Standardisation and High Reproducibility
– Lot to Lot Consistency
– Accuracy and Precision

Validated against seven points for a Gold Ring Standard Quality Assay – the benchmark sign for Krishgen quality.









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Additional information

Pack Type

15 ml / 450 tests
Species

Ruminants
Sample Type

Serum, Plasma
Assay Range

Qualitative, screening assay
Sensitivity

>98%
Interference

Preparations of the known factors were assayed for interference. No significant interference was observed.
Specificity

This assay recognises both the recombinant and natural protein
Principle Of Assay

Immunochromatography
Detection Method

Visual Read
Conjugate - Enzyme Reaction

Uses Colloidal Gold / Color Beads conjugate for color development
Regulatory Status

For In-Vitro Testing Only
Shipping Temperature

Room Temperature / 2-8 degrees Celsius
Storage Temperature

The kit and its components are to be stored as indicated in the IFU (instructions for use). To ensure quality of your results, if all the wells in the kit are not being used, store the unused wells in the foil pouch containing the desiccant pack, well sealed and store at the indicated temperature.
ELISA Type

Immunochromatography, Double Antibody
ELISA Interpretation

Positive Control Line, Test Control Line color development for visual read and checking
Shelf Life Available

12 months at time of shipping
Alternate Names / Synonyms

Brucellosis Bengal Rose Plate
Research Area

Animal, Pet, Lab Animal testing
Disclaimer

The data indicated herein with specifications are changed from time to time at time of production of the assay. We request you to confirm the specifications including the assay range and procedure as per the most current IFU (instructions for use) accompanying the assay kit.

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