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Cell Proliferation Assay Cocktail

Cell Proliferation Assay Cocktail

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Specification

Product name Cell Proliferation Assay Cocktail
Applications notes Cell Proliferation Assay Cocktail can not only accurately detect cell proliferation status directly from DNA level, but also realize high-throughput detection of cell proliferation status through cell metabolism level. It is a universal cell proliferation detection product.

Product Properties

Kit components
•EdU Cell Proliferation Image Kit (Green Fluorescence)-100T
EdU (10 mM)
BSA Wash Solution (5×)
AbFluor 488 azide
10×Reaction buffer
Copper Reagent
Reducing Agent
DAPI (500×)
•Cell Counting Kit-8 (CCK-8)-2000T
CCK-8
•Postive Control-100T
Postive Control
Features & Benefits • Standardized: The patented cytotoxicity positive reference substance can perfectly solve the problem of non-standardization of proliferation/toxicity test results at present.
• Universal: It can detect cell proliferation status most directly and accurately, and it can be also chosen as high-throughput detection detection, which covers most cell proliferation/toxicity detection needs.
Storage instructions Refer to list of materials supplied for storage conditions of individual components.
Shipping Blue ice
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background Cell proliferation is a process of increasing the number of cells by means of cell division, which will produce many important changes, including the synthesis of DNA, the increase of cell metabolism, the expression of proliferation-specific proteins and so on.

Image & description

Fig.1. HEK293 and L929 cells in the positive control group were induced by cytotoxicity inducer for 30 min, while the control group was not given any treatment. Enhanced Cell Counting Kit-8 (CCK-8) was used to detect the cytotoxicity of HEK293 and L929 cells after cytotoxicity induction.

Fig.1. HEK293 and L929 cells in the positive control group were induced by cytotoxicity inducer for 30 min, while the control group was not given any treatment. Enhanced Cell Counting Kit-8 (CCK-8) was used to detect the cytotoxicity of HEK293 and L929 cells after cytotoxicity induction.

Fig.2. Cell Proliferation EdU Image Kit (Green Fluorescence) was used to detect the cytotoxicity of HEK293 cells after cytotoxicity induction.

Fig.2. Cell Proliferation EdU Image Kit (Green Fluorescence) was used to detect the cytotoxicity of HEK293 cells after cytotoxicity induction.

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