FN-Click EdU Cell Proliferation Flow Cytometry Assay Kit (Green, FineTest®488)

Cat# FNCK107-200T

Size : 200T

Brand : FineTest

Contact local distributor :


Phone : +1 850 650 7790

Catalogue No.: 
FNCK107
Size: 
50T/200T
Storage: 
Store at -20°C for 1 year.FineTest®488 Azide I needs to be stored away from light.
Application: 
Cell Proliferation
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Dispatch Time: About 3 working days
Catalog No.

FNCK107

Size

50T/200T

Kit components

Cat.

Reagents

50T

200T

FNCK107A

EdU(10mM)

200μL

800μL

FNCK107B

Click Reaction Buffer I

25mL

50mL*2

FNCK107C

FineTest®488 Azide I

50μL

200μL

FNCK107D

CuSO4

1mL*2

8mL

FNCK107E

Click Additive

220mg

220mg*4

Note: 50 T means that 50 samples can be tested with 6 well plates. EdU (10 mM) needs to be stored in aliquots for the first use(50 μL/ vial is recommended or aliquot into smaller quantities according to experimental needs).

Storage

Store at -20°C for 1 year.FineTest®488 Azide I needs to be stored away from light.

Description

FN-Click EdU Cell Proliferation Flow Cytometry Assay kit (green, FineTest®488) is convenient and sensitive for proliferation detection of cell suspension samples. The results can be analyzed by flow cytometry.

Cell proliferation detection is widely used in the evaluation of cell activity, genotoxicity and efficacy of anti-tumor drugs. Direct detection of DNA synthesis in cells is considered to be the most accurate method to detect cell proliferation.The first widely used method to detect DNA synthesis in cells was the radionuclide incorporation method, but this method was greatly limited due to radioactive contamination and the difficulty of single-cell detection, and it was gradually replaced by the BrdU method based on antibody detection. BrdU method has many steps and requires the use of BrdU antibody, which has many influencing factors and poor stability.

EdU method is based on EdU incorporation and subsequent click reaction, without the use of antibodies, convenient operation, high detection sensitivity, is a new method to upgrade on the basis of BrdU method, will gradually replace BrdU method. EdU(5-ethynyl-2-deoxyuridine) is a thymine deoxyriboside analogue that can be incorporated into newly synthesized DNA in place of thymine deoxyriboside during DNA synthesis. On the other hand, the acetylene group on EdU can covalently react with a fluorescently labeled small molecule azide probe to form a stable triazole ring catalyzed by a monovalent copper ion, which is a very rapid reaction known as the Click reaction.Through the click reaction, the newly synthesized DNA is labeled with a corresponding fluorescent probe, so that the proliferating cells can be detected using appropriate fluorescence detection equipment.

Test results refer to the figure below:

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