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  • Cell Cycle and Apoptosis Analysis Kit

    Product No.:C6031

    Product specification:50T/100T

    Catalogue price(RMB):350/600

    Can replace similar products in the market

    Bulk Request


Product overview:

Contents

Component

50T

100T

A.1× Binding buffer

25 mL

50 mL

B. PI Staining Solution (20×)

1.25 mL

2.5 mL

C. RNase A (50×)

0.5 mL

1 mL


Storage 

Store at 4℃. When stored as directed, product is stable for at least 12 months. Store at -20℃. When stored as directed, product is stable for at least 24 months. PI needs to be protect from light.

Description 

Analysis of nucleic acids is a common application of flow cytometry. Measurement of DNA content allows the study of cell populations in various phases of the cell cycle as well as the analysis of DNA ploidy. In a given population, cells will be distributed among three major phases of cell cycle: G0/G1 phase (one set of paired chromosomes per cell), S phase (DNA synthesis with variable amount of DNA), and G2/M phase(two sets of paired chromosomes per cell, prior to cell division).DNA content can be measured using fluorescent DNA stains that exhibit emission signals proportional to DNA mass. Flow cytometric analysis of these stained populations is then used to produce a frequency histogram that reveals the various phases of the cell cycle. Univariate DNA content analysis is an established assay method and is widely used for studies in oncology, cell biology, and molecular biology.

Propidium iodide (PI) Staining Solution is used for flow cyotmetric analysis of DNA content in fixed cells., PI ,a popular red-fluorescent stain, binds to DNA by intercalating between the bases with little or no sequence preference and with a stoichiometry of one dye per 4–5 base pairs of DNA. PI also binds to RNA, necessitating treatment with RNase to distinguish between RNA and DNA staining.


Instructions:


   UE-C6031

Citations and references:


1.DRP1 upregulation promotes pancreatic cancer growth and metastasis through increased aerobic glycolysis

Jing Liang,Yiping Yang,Lu Bai,Feng Li,Enxiao Li

J Gastroenterol Hepatol.

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