Bioendo KC Endotoxin Test Kit (Kinetic Chromogenic Assay)

Bioendo KC Endotoxin Test Kit (Kinetic Chromogenic Assay)

1. Product Information

In Bioendo KC Endotoxin Test Kit, Amebocyte Lysate is co-lyophilized with chromogenic substrate. Therefore, bacterial endotoxin could be quantified based on the chromogenic reaction. The assay is strong resistance to interference, and has advantages of kinetic turbidimetric and end-point chromogenic method. Bioendo Endotoxin Test Kit contains Chromogenic Amebocyte Lysate, Reconstitution Buffer, CSE, Water for BET. Endotoxin detection with Kinetic Chromogenic method requires a kinetic incubating microplate reader such as ELx808IULAL-SN.

2. Product Parameter

Assay Range: 0.005 – 50EU/ml; 0.001 – 10EU/ml

3. Product Feature and Application

Bioendo^TM KC Endotoxin Test Kit (Kinetic Chromogenic Assay) features strong resistance to interference, and has advantages of kinetic turbidimetric and end-point chromogenic method. It is especially suitable for endotoxin detection of biological samples like vaccine, antibody, protein, nucleic acid, etc.

Note:

Lyophilized Amebocyte Lysate reagent manufactured by Bioendo is made from amebocyte lysate from the horseshoe crab (Tachypleus tridentatus).

Product Condition:

The sensitivity of Lyophilized Amebocyte Lysate and potency of Control Standard Endotoxin are assayed against USP Reference Standard Endotoxin. The Lyophilized Amebocyte Lysate reagent kits come with product instruction, Certificate of Analysis. 

The kinetic chromogenic endotoxin test kit have to choose the microplate reader with 405nm filters.

The Kinetic chromogenic lal assay utilizes innovative chromogenic technology to provide accurate results up to 0.005EU/ml, making it the ideal choice for those drug test in the laboratories. This assay is designed to detect endotoxin levels in a wide range of samples, including pharmaceutical products, medical devices, and environmental samples.

One of the key features of the KCA assay is its kinetic nature, which allows for real-time monitoring of endotoxin levels. This means that users can track the progress of the assay as it is being performed, providing valuable insights into the kinetics of endotoxin detection. This real-time data can help users make informed decisions about the quality and safety of their products, ultimately leading to improved outcomes and customer satisfaction.

Additionally, the chromogenic lal assay offers unparalleled sensitivity and specificity, ensuring that even low levels of endotoxin can be accurately identified and quantified. This high level of precision is essential for ensuring the safety and efficacy of pharmaceutical products and medical devices, as endotoxin contamination can have serious health implications for patients and consumers.

Furthermore, the KCA assay is simple and user-friendly, requiring minimal hands-on time and training. This makes it an ideal solution for laboratories with high sample volumes or limited resources, as it can streamline the endotoxin testing process and improve overall efficiency. The KCA LAL assay can also be easily integrated into existing laboratory workflows, minimizing disruption and saving valuable time and resources.

In summary, the Kinetic Chromogenic LAL Endotoxin Test Assay (KCA) is a quantitative endotoxin test assay that offers unmatched accuracy, speed, and ease of use. Its unique kinetic chromogenic technology and real-time monitoring capabilities set it apart from traditional endotoxin detection methods, making it the top choice for researchers, healthcare professionals, and pharmaceutical companies. With the KCA assay, users can confidently ensure the safety and quality of their products, leading to improved outcomes and customer satisfaction. Experience the next generation of endotoxin testing with the KCA assay.