The QUALICHEK Clenbuterol ELISA includes features like:
– Ready to use protocol with break-apart wells for ease of use
– Standardisation and High Reproducibility
– Lot to Lot Consistency
– Accuracy and Precision

Validated against seven points for a ?GOLD RING? Standard Quality ELISA – the benchmark sign for Krishgen Quality. The QUALICHEK ELISA kits are validated in the sample matrices indicsted. The kit uses recombinant antibodies to ensure a high degree of sensitivity and specificity in he assay.

Pack Type	1 x 96 wells, break-apart
Sample Matrix	Meat
Assay Range	Tissue (method 2): 0.1 – 8.1 ppb; Tissue (method 1): 0.4 – 32.4 ppb; Feed: 1 – 81 ppb, Urine
Standards Available	0; 1.012; 2.025; 4.05; 8.1; 16.2; 32.4 ppb
Interference	Preparations of the known factors were assayed for interference. No significant interference was observed.
Principle Of Assay	resulting in a lower signal. So, signal intensity is inversely proportional to the concentration of the target antigen., the less labeled antigen is bound, the sample / standard antigen competes with a labeled antigen for a limited amount of capture monoclonal antibody. The more antigen present in the sample
Detection Method	Absorbance measured at 450nm, Colorimetric
Conjugate-Enzyme Reaction	and dynamic range, balancing speed, sensitivity
Quality Certification	ISO13485 certified facility., Validated as per KRISHGEN's Quality Program. We are and ISO9001
KRISHGEN Mandate	High Performance Assays at Affordable Prices
Regulatory Status	For Research Use Only (RUO).
Shipping Temperature	Shipped at Room Temperature or in gel pack to maintain temperature at 2-8 degrees Celsius
Storage Temperature	if all the wells in the kit are not being used, store the unused wells in the foil pouch containing the desiccant pack, The kit (2-8 Degree Celsius) and its components are to be stored as indicated in the IFU (instructions for use). To ensure quality of your results
Application Area	Analysis?of the analyte/marker in Tissue, Feed, serum, Urine
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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