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FMOC isothiocyanate 97%

Lieferant: Thermo Fisher Scientific

Beschreibung: FMOC isothiocyanate 97%

Sicherheitsdatenblätter

4-(Dimethylamino)azobenzene-4'-isothiocyanate 97%, Sigma-Aldrich®

Lieferant: SIGMA ALDRICH MICROSCOPY

Beschreibung: 4-(4-Isothiocyanatophenylazo)-N,N-dimethylaniline,97% (4-(Dimethylamino)azobenzene-4'-isothiocyanate; DABITC)

Rhodamine B isothiocyanate–Dextran

Artikel-Nr: (R8881-100MG)

Lieferant: SIGMA ALDRICH MICROSCOPY

Hersteller Artikel Nummer : R8881-100MG

Beschreibung: Rhodamine B is a thiol-reactive and photostable fluorescent dye. Rhodamine B isothiocyanate is an aminoxanthene that possesses carboxylic acid and isothiocyanate substituents on the pendant phenyl ring.

UOM: 1 * 100 mg

Sale

N/A Each

9-Fluorenylmethylchlorformiat (Fmoc-Chlorid) zur Synthese

Lieferant: Merck

Beschreibung: 9-Fluorenylmethylchlorformiat (Fmoc-Chlorid) zur Synthese

Sicherheitsdatenblätter Zertifikate

9-Fluorenylmethylchlorformiat (Fmoc-Chlorid), Supelco®

Lieferant: Merck

Beschreibung: 9-Fluorenylmethylchlorformiat (Fmoc-Chlorid), Supelco®

Zertifikate

Fluorescein isothiocyanate (mixture of 5 and 6 isomers) ≥90% (durch HPLC), Sigma-Aldrich®

Artikel-Nr: (F3651-100MG)

Lieferant: SIGMA ALDRICH MICROSCOPY

Hersteller Artikel Nummer : F3651-100MG

Beschreibung: Fluorescein isothiocyanate (FITC) is widely used to attach a fluorescent label to proteins via the amine group. The isothiocyanate group reacts with amino terminal and primary amines in proteins. It has been used for the labeling of proteins including antibodies and lectins.

UOM: 1 * 100 mg

Sale

N/A Each

Tetramethylrhodamine isothiocyanate Isomer R (6-TRITC isomer R), Sigma-Aldrich®

Lieferant: SIGMA ALDRICH MICROSCOPY

Beschreibung: 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.