Hoechst 34580 [23555-00-2]

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Referência NB-64-08931-2mg

Tamanho : 2mg

Marca : Neo Biotech

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Hoechst 34580 (Synonyms: HOE 34580)

Catalog No. T19011 Copy Product Info
Purity: 98.53%
Hoechst 34580 (HOE 34580), a cell-permeable fluorescent dye, is used for staining DNA and nuclei.

Hoechst 34580

Copy Product Info
Synonyms HOE 34580

Hoechst 34580 (HOE 34580), a cell-permeable fluorescent dye, is used for staining DNA and nuclei.

Hoechst 34580
Cas No. 23555-00-2
Select Batch
Purity:98.53%
Appearance:Solid
Color:Yellow
Contact us for more batch information

Product Introduction

Bioactivity
Description
Hoechst 34580 (HOE 34580), a cell-permeable fluorescent dye, is used for staining DNA and nuclei.
In vitro
Hoechst 34580 is a good candidate for treating Alzheimer's disease by inhibiting Aβ formation. 50 μM Aβ42 solutions co-incubated with 100, 25, 12.5, 3.125, 0.78, and 0.1, 0.01 μM Hoechst 34580 at 37 °C for 70 h. Hoechst 34580 can inhibit the aggregation of Aβ42 in a dose-dependent manner. The IC50 is obtained by measuring the concentration of Hoechst 34580 while maintaining the Aβ42 concentration which gave 0.86±0.05 μM for Hoechst 34580.
Cell Research
Instructions:
I. Solution preparation
1. Preparation of stock solution: Prepare 1 mg/mL Hoechst 34580 stock solution with DMSO.
Note: It is recommended to store Hoechst stock solution at -4℃ or -20℃ in the dark after aliquoting.
2. Preparation of working solution: Dilute the stock solution with pure DMEM or PBS before use, and the final concentration is 10 μg/mL Hoechst working solution.
Note: Please adjust the concentration of Hoechst working solution according to actual conditions and prepare it before use.
II. Cell staining (suspended cells)
1. Collect cells by centrifugation and wash twice with PBS for 5 minutes each. The cell density is 1×10^6/mL
2. Add 1 mL Hoechst working solution and incubate at room temperature for 3-10 minutes.
3. Centrifuge at 400 g for 3-4 minutes and discard the supernatant.
4. Add PBS to wash cells twice for 5 minutes each.
5. Resuspend the cells with 1 mL serum-free medium or PBS, and observe using a fluorescence microscope or flow cytometer.
III. Cell staining (adherent cells)
1. Culture the adherent cells on a sterile coverslip.
2. Remove the coverslip from the culture medium and remove the excess culture medium.
3. Add 100 μL of dye working solution, gently shake to completely cover the cells, and incubate for 3-10 minutes.
4. Aspirate the dye working solution, wash with culture medium 2-3 times, 5 minutes each time, and observe using a fluorescence microscope or flow cytometer.
Precautions
1. Please adjust the concentration of Hoechst working solution according to your actual situation.
2. This product is limited to scientific research by professionals and shall not be used for clinical diagnosis or treatment, nor for food or medicine.
3. For your safety and health, please wear a lab coat and disposable gloves when operating.

The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands.
SynonymsHOE 34580
Chemical Properties
Molecular Weight451.57
FormulaC27H29N7
Cas No.23555-00-2
SmilesCN(C)c1ccc(cc1)-c1nc2cc(ccc2[nH]1)-c1nc2cc(ccc2[nH]1)N1CCN(C)CC1
Relative Density.1.280 g/cm3 (Predicted)
Storage & Solubility Information
StorageShipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 47 mg/mL (104.08 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2145 mL11.0725 mL22.1450 mL110.7248 mL
5 mM0.4429 mL2.2145 mL4.4290 mL22.1450 mL
10 mM0.2214 mL1.1072 mL2.2145 mL11.0725 mL
20 mM0.1107 mL0.5536 mL1.1072 mL5.5362 mL
50 mM0.0443 mL0.2214 mL0.4429 mL2.2145 mL
100 mM0.0221 mL0.1107 mL0.2214 mL1.1072 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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Referência
Descrição
Cond.
Price Bef. VAT
LIN-END9000-100
 100ml 
NB-64-30238-1mL
 1mLx10mM(inDMSO)