Cresol Red sodium
Cresol Red sodium is a colorimetric pH indicator. Cresol Red sodium serves as an optical sensor for monitoring carbonic anhydrase-catalyzed reactions and as a colorimetric dye that responds to hydrogen ions generated during DNA synthesis. Cresol Red sodium can be used in the research of hepatitis A and COVID-19.
For research use only. We do not sell to patients.
- CAS No.: 62625-29-0
- Formula: C21H17NaO5S
- Molecular Weight:404.41
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Storage:
RT, protect from light, stored under nitrogen.
In solvent -80°C, 1 year , -20°C, 6 months
Biological Activity
Description
In Vitro
Cresol Red sodium (3.71 mM; 6 h) enables naked-eye detection of temperature changes through visualizable DNA synthesis, allowing detection of short-term temperature exposure lasting only 2 h in cold-chain logistics while ensuring stability at room temperature[2].
Cresol Red sodium salt serves as a pH indicator in solution for colorimetric RT-LAMP detection of the SARS-CoV-2 N gene[11].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Emission (Em)
689
Chemical Information
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CAS No. 62625-29-0
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Appearance Solid
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Molecular Weight 404.41
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Formula C21H17NaO5S
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Color Brown to dark brown
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SMILES
O=S1(OC(C2=CC=C(O[Na])C(C)=C2)(C3=CC=C(O)C(C)=C3)C4=CC=CC=C41)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
RT, protect from light, stored under nitrogen
In solvent -80°C 1 year -20°C 6 months
Protocols
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EdU Incorporation Assay (Click Chemistry-Based DNA Synthesis Measurement)
The EdU incorporation assay measures DNA synthesis by adding the thymidine analog 5-ethynyl-2′-deoxyuridine to cells or tissues, where it is incorporated into newly synthesized DNA during S phase. Incorporated EdU is detected by copper-catalyzed azide-alkyne cycloaddition, in which a fluorescent azide covalently reacts with the ethynyl group on EdU, allowing S-phase cells to be detected by fluorescence microscopy, flow cytometry, or high-content imaging. EdU detection does not require DNA denaturation or anti-BrdU antibody access, which preserves sample structure and improves compatibility with immunostaining and multiparameter cytometry compared with BrdU-based detection. EdU can be cytotoxic in a cell-type- and exposure-dependent manner, so pulse duration, concentration, and continuous-labeling designs should be validated for each cell type.
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BrdU Incorporation Assay
Bromodeoxyuridine (BrdU) incorporation assay is based on the principle that BrdU, a thymidine analog, is incorporated into newly synthesized DNA during the S phase of the cell cycle, thereby serving as a marker of DNA replication and cellular proliferation. Incorporated BrdU can be detected using anti-BrdU antibodies following DNA denaturation, enabling visualization or quantification of proliferating cells through immunochemical detection methods such as immunofluorescence or immunohistochemistry.
Purity & Documentation
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Data Sheet (282 KB)
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SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)