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BioReagent,Biological Stain,for fluorescence analysis,for microscopy,≥90% Biological Stain,BioReagent,for Fluorescence analysis,for Microscopy for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
FITC and TRITC are among the most simple and commonly used reagents for protein fluorescent labeling. These isothiocyanates will crosslink to amino, sulfhydryl, imidazoyl, tyrosyl or carbonyl groups on a protein. However, only the derivatives of primary and secondary amines generally yield stable products. Reactions are most efficient at pH 8-9, and must be performed in an amine-free buffer such as carbonate/bicarbonate. Avoid Tris buffer, which is a primary amine that will compete with the intended labeling reaction. Antibody and other proteins can be effectively labeled with several fluorophore tags per protein molecule when reacted with a 20- to 25-fold molar excess of isothiocyanate-activated fluorophore. Excess nonreacted and hydrolyzed reagent can be removed by dialysis or gel filtration.
Extinction Coeff: 100,000 M⁻¹ cm⁻¹ (at 544 nm in methanol); Ex/Em Wavelength =541/572 nm
Procedure for Labeling an Antibody with TRITC
This method is adapted from Larsson²
Materials Required
1. TRITC: dissolve in DMSO at 1 mg/ml
2. Conjugation buffer: 100 mM carbonate/bicarbonate buffer, pH 9.0
3. Antibody solution: dialyze antibody into conjugation buffer at 6 mg/ml
Procedure
1. While stirring, slowly add 35 μl of TRITC to 1 ml of the 6 mg/ml antibody solution; mix thoroughly.
2. Incubate for 2 hours at room temperature in the dark.
3. Remove excess and hydrolyzed TRITC by gel filtration.
Additional Information
Fading (photobleaching in tissue sections) can sometimes be reduced by mounting in an alkaline buffered media (pH 9).² There are several reagents that may be used with FITC and/or TRITC derivatives to prevent fading including n-propylgallate at 0.1-0.25 M dissolved in glycerol for FITC or TRITC.³ For FITC derivatives, o- or p-phenylenediamine added to the mounting buffer from 1 μg/ml to 1 mg/ml in glycerin also may be used.²³
References
1. Horisberger, M. 1984. In Immunolabeling for Electron Microscopy. Polak, J., Varndel, I. Ed. Elsevier: Amsterdam, p. 98.
2. Larsson, L. (1988). Immunocytochemistry: Theory and Practice. CRC. Boca Raton, 77-83, 224-225.
3. Goding, J. (1986). Monoclonal Antibodies: Principles and Practice, 2nd ed. Academic, London.
| Isomeric SMILES | CN(C)C1=CC2=C(C=C1)C(=C3C=CC(=[N+](C)C)C=C3O2)C4=C(C=C(C=C4)N=C=S)C(=O)[O-] |
|---|---|
| PubChem CID | 2762684 |
| Molecular Weight | 443.518 |
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| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | May 08, 2026 | T639043 | |
| Certificate of Analysis | May 08, 2026 | T639043 |
| Sensitivity | Light-sensitive |
|---|
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