"SIGMA ALDRICH MICROSCOPY"
Pararosaniline acetate 90% (dye content), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Pararosaniline acetate, Dye content 90% (Basic Parafuchsin; Basic Red 9; Magenta(TM) O).
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Sigmacote® siliconizing reagent
Supplier: SIGMA ALDRICH MICROSCOPY
Siliconizing reagent for glass and other surfaces. Sigmacote® is a solution of a chlorinated organopolysiloxane in heptane that readily forms a covalent, microscopically thin film on glass.
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Safranine O ≥85% (dye content), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Safranin O is a cationic dye, which displays less significant metachromasia. It is used to detect any variations in articular disease. Safranin O binds specifically to polyanions. It detects the amount of proteoglycan present in cartilages. Safranin O is used as a marker for glycosaminoglycan depletion in osteoarthritis. Safranin is used as a counter stain in gram staining.
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trans-4-Hydroxycinnamic acid ≥98% (by HPLC), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
p-Coumaric acid has been used as a component of chemiluminescent substrate for protein detection in western blotting.
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Sudan red G in toluene, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Sudan red G in toluene, Sigma-Aldrich®
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Direct Blue 15, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
May be used as a substitute for trypan blue for some biological and staining applications.
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4-Formylbenzene-1,3-disulphonic acid disodium salt hydrate 97%, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
4-Formylbenzene-1,3-disulfonic acid disodium salt hydrate,97% (Benzaldehyde 2,4-disulfonic acid disodium salt; Sodium 4-formylbenzene-1,3-disulfonate).
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Fluorescein 95% (dye content), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Fluorescein 95% (dye content), Sigma-Aldrich®
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4-Amino-3-hydroxy-1-naphthalenesulphonic acid in ACS Reagent grade water ≥90%, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
4-Amino-3-hydroxy-1-naphthalenesulfonic acid is a derivative of aniline consisting of a trifunctional monomer (bearing three functional groups –NH₂, –OH and –SO₃H). It also contains two fused benzene rings.
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Acid red 52, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Sulforhodamine B has been used as a dye in the MCF-7 (human breast adenocarcinoma cell line) cell proliferation assay.
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Rose Bengal ≥80% (dye content), certified by the Biological Stain Commission, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Rose bengal,certified by the Biological Stain Commission, Dye content ≥80 % (4,5,6,7-Tetrachloro-2',4',5',7'-tetraiodofluorescein disodium salt; Acid Red 94; Bengal Rose B sodium salt; Rose Bengal sodium salt).
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Haematoxylin (Harris), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
General purpose nuclear stain, regressive type. Used with hematoxylin and eosin staining.
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Eosin Y ∼99% (dye content), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Eosin Y is a xanthene dye and is used for the differential staining of connective tissue and cytoplasm. In histopathology, it is applied as a counterstain after hematoxylin and before methylene blue. It is also used as a background stain, thereby giving contrast to the nuclear stains.
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Lucifer yellow CH dilithium salt for fluorescence Stain, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
A highly fluorescent dye, useful in marking nerve cells.
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Stains-all ~95%, Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Stains-All has been used for the staining of gel made for size determination of hyaluronan. It has also been used for the staining of DNA oligonucleotides separated by nondenaturing polyacrylamide gel electrophoresis.
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Tetramethylrhodamine isothiocyanate Isomer R (6-TRITC isomer R), Sigma-Aldrich®
Supplier: SIGMA ALDRICH MICROSCOPY
Tetramethylrhodamine isothiocyanate Isomer R (TRITC) is the R isomer of tetramethylrhodamine isothiocyanate and is also known as 6-tetramethylrhodamine isothiocyanate. It is a strongly fluorescent compound soluble in ethanol, methanol, dimethylformamide, dimethylsulfoxide, and water. TRITC is a moderately-sized aminoxanthene dye carrying carboxylic acid and isothiocyanate substituents on the non-planar pendant phenyl ring. It forms a lipophilic cation in acidic pH and a hydrophilic zwitterion around neutral pH. The isothiocyanate group reacts with nucleophilic substituents (e.g., amino, hydroxyl, thiol) of biomolecules, providing the means of attaching a fluorescent label. TRITC also reacts with water and hydroxide ions and is unstable in aqueous solutions. TRITC is commercially available as a zwitterion or as a chloride.
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