HOE-S 785026

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¥ 21,000.90 21000.9 CNY ¥ 21,000.90

¥ 3,500.90

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规格或纯度 ≥99%
货号(SKU) H651699
品牌 阿拉丁
  • 包装

此组合不存在。

条款和条件
30天退款保证
运输:2-3 个工作日

规格


Cas Number 132869-83-1
规格或纯度 ≥99%
纯度 ≥99%
包装 100mg50mg10mg5mg

产品信息


品牌 阿拉丁
溶解性 DMSO : ≥ 37 mg/mL (87.16 mM)
过滤标签 Fluorescent Dye
储存温度 避光,-80℃储存
运输条件 超低温冰袋运输
生化和生理学机理 HOE-S 785026 是 Hoechst 系列中的一种标记染料。Hoechst 是一种活的核标记染料。Hoechst 可与 DNA 双链的沟槽结合,这种双链往往是富含 A/- T 的 DNA 链。虽然它能与所有核酸结合,但富含 A/- T 的双链 DNA si
英文描述

HOE-S 785026 is a marker dye in Hoechst series. Hoechst is A live nuclear marker dye. Hoechst binds to the grooves in the DNA double strand, which tends to be A/ T-rich DNA strand. Although it binds to all nucleic acids, the A/ T-rich double strand DNA significantly enhances fluorescence intensity Therefore,Hoechst dye can be used for living cell labeling. The fluorescence intensity of Hoechst dye increases with the increase of pH of solution.

In Vitro

General Protocol Preparation of Hoechst working solution 1.1 Preparation of the stock solution Dissolve 10 mg of in 5 mL ddH 2 O Note: It is recommended to store the stock solution at 4°C or -20°C away from light and avoid repetitive freeze-thaw cycles. 1.2 Preparation of Hoechst working solution Dilute the stock solution in serum-free cell culture medium or PBS to obtain final concentration 10 μg/mL Hoechst working solution. Note: Please adjust the concentration of Hoechst working solution according to the actual situation. 1.Cell staining 2.1 Suspension cells(6-well plate) a. Centrifuge at 1000 g at 4°C for 3-5 minutes and then discard the supernatant. Wash twice with PBS, 5 minutes each time.The cell density is 1×10 6 /mL. b. Add 1 mL of working solution, and then incubate at room temperature for 3-10 minutes. c. Centrifuge at 400 g at 4°C for 3-4 minutes and then discard the supernatant. d. Wash twice with PBS, 5 minutes each time. e. Resuspend cells with serum-free cell culture medium or PBS. Observation by fluorescence microscopy or flow cytometry. 2.2 Adherent cells a. Culture adherent cells on sterile coverslips. b. Remove the coverslip from the medium and aspirate excess medium. c. Add 100 μL of working solution, gently shake it to completely cover the cells,and then incubate at room temperature for 3-10 minutes. d. Wash twice with medium, 5 minutes each time.Observation by fluorescence microscopy or flow cytometry. Storage 4°C, 1 year. Protect from light Precautions 1. Please adjust the concentration of Hoechst working solution according to the actual situation. 2. This product is for R&D use only, not for drug, household, or other uses. 3. For your safety and health, please wear a lab coat and disposable gloves to operate. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

技术规格说明书


质检证书(CoA,COO,BSE/TSE)