H2DCFDA NEW
| Price | $37 | $50 |
| Package | 50mg | 100mg |
| Supply Ability: | 10g |
| Update Time: | 2026-05-22 |
Product Details
| Product Name: H2DCFDA | CAS No.: 4091-99-0 |
| Purity: 97.04% | Supply Ability: 10g |
| Release date: 2026/05/22 |
Product Introduction
Bioactivity
| Name | H2DCFDA |
| Description | H2DCFDA (DCFH-DA) belongs to the class of green fluorescent dyes and is a probe for the detection of intracellular reactive oxygen species (ROS) (Ex/Em=488/525 nm) with cell membrane permeability. |
| Cell Research | Instructions: I. Solution preparation 1. Prepare storage solution: Prepare 10 mM H2DCFDA stock solution with DMSO. Note: It is recommended to store H2DCFDA storage solution at -20 ℃ or -80 ℃ in the dark after aliquoting. 2. Preparation of working solution: Dilute the storage solution with preheated serum-free cell culture medium or PBS to prepare 1-10 μM H2DCFDA working solution. Note: Please adjust the concentration of H2DCFDA 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 of dye working solution and incubate at room temperature for 5-30 minutes. 3. Centrifuge at 400 g for 3-4 minutes and discard the supernatant. 4. Add PBS to wash the cells twice, 5 minutes each time. 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 5-30 minutes. 4. Aspirate the dye working solution, wash 2-3 times with culture medium, 5 minutes each time, and observe using a fluorescence microscope or flow cytometer. Note: If flow cytometry is required, the cells need to be digested with trypsin and resuspended before staining. The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands. |
| In vitro | METHODS: Flow cytometry was used to detect ROS levels: 1, H2DCFDA was dissolved into 10 mM DMSO stock solution and further diluted with PBS before use. 2. Adherent cells are incubated with 5 μM H2DCFDA solution for 30 min at 37°C, protected from light, then harvested with 0.05% trypsin-EDTA solution, suspended in fresh medium and immediately analyzed by flow cytometry (488 nm). [1] METHODS: Confocal microscopy was performed to detect ROS levels: 1. H2DCFDA was dissolved into 10 mM DMSO stock solution and further diluted with PBS before use. 2. Coverslips containing cells were placed in 5 μM H2DCFDA staining solution and incubated for 60 min at 37°C, protected from light, then washed and imaged with a confocal laser scanning microscope Leica TCS SL equipped with an argon laser. [1] The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands. |
| In vivo | METHODS: Fluorescence microscopy was used to analyze the oxidative activity of LPS induced peritonitis in mice: 1, H2DCFDA was dissolved in 100 μL ethanol and further diluted with PBS before use. 2. C57BL/6J mice were injected intraperitoneally with LPS (0.1-1 mg/mL) to induce peritonitis. 3.5 h later, H2DCFDA (0.1-0.8 mg/ml) was injected intraperitoneally. 3. 30 min after H2DCFDA injection, the animals were killed by cervical dislocation, and the peritoneal cells were recovered by rinsing with 5 mL of ice-cold HBSS solution at pH 7.4. 4. Peritoneal cells were washed and resuspended in PBS. Macrophages were removed by adhesion method after incubation in a polystyrene dish at 37℃ for 30 min. The supernatant was recovered and approximately 20,000-25,000 leukocytes were added to microscope slides using a cytocentrifuge. The slides were then analyzed using fluorescence microscopy. [2] |
| Storage | Keep away from direct sunlight,Store at low temperature,Keep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | Ethanol : 14.29 mg/mL (29.33 mM), Sonication is recommended. DMSO : 257.5 mg/mL (528.43 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 5 mg/mL (10.26 mM), Solution. |
| Keywords | ReactiveOxygenSpecies | Reactive Oxygen Species | Inhibitor | inhibit | H-2DCFDA | H2DCFDA | 2',7'-Dichlorodihydrofluorescein Diacetate | 2',7'-Dichlorodihydrofluorescein |
| Inhibitors Related | Ethoxyquin | Kaolin | Allopurinol | Cysteamine hydrochloride | Imeglimin hydrochloride | Ethyl linoleate | Magnesium acetate tetrahydrate | Inosine | L-Cystine | Dimethyl itaconate | L-Ascorbic acid sodium salt | Dimethyl phthalate |
| Related Compound Libraries | NF-κB Signaling Compound Library | Bioactive Compound Library | Anti-Ovarian Cancer Compound Library | Anti-Breast Cancer Compound Library | Pyroptosis Compound Library | Mitochondria-Targeted Compound Library | NO PAINS Compound Library | Anti-Aging Compound Library | Immunology/Inflammation Compound Library | Bioactive Compounds Library Max | Anti-Cancer Compound Library | Oxidation-Reduction Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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