You Searched For: SIA+(N-Succinimidyl+iodoacetate)

Catalog Number: (BC96)

Supplier: G-Biosciences

Description: SATA reacts with primary amines, adding protected sulphhydryl residues. It is soluble in DMSO and the sulphhydryl group can be used in coupling reactions.

UOM: 1 * 100 mg

Supplier: Alfa Aesar

Description: D-Biotin-N-succinimidyl ester ≥98%

Supplier: APOLLO SCIENTIFIC

Description: N-Succinimidyl [(tert-Butoxycarbonyl)aminooxy]acetate 98%

Catalog Number: (40075.)

Supplier: Biotium

Description: The amine reactive succinimidyl ester of MB (methylene blue) can be conjugated to peptides, proteins, drugs, polymeric materials and biomolecules with primary amine groups. The conjugate will have a blue color and be able to complex with nucleic acids. Methylene blue is a well known redox dye which can be reversibly reduced to its colorless leuco form. Upon oxidation, the blue color of the dye is recovered.

UOM: 1 * 5 mg

Supplier: APOLLO SCIENTIFIC

Description: Primary amine and Sulphhydryl reactive, Enzyme antibody conjugation.

Catalog Number: (90117-1MG)

Supplier: Biotium

Description: Cyanine NS succinimidyl esters are non-sulfonated cyanine dyes that can be used to label proteins, oligonucleotides and nucleic acids. Available in 3 colors, Cyanine 488NS, Cyanine 555NS, and Cyanine 647NS are designed to match by charge and molecular weight for 2D DIGE platform.

UOM: 1 * 1 mg

Supplier: APOLLO SCIENTIFIC

Description: alpha-(9-Fluorenylmethyloxycarbonyl)amino-omega-carboxy succinimidyl ester PEG

Catalog Number: (90031.)

Supplier: Biotium

Description: Amine-reactive form of single isomer carboxyrhodamine 110. For certain applications, the dye is preferred over the corresponding 6-carboxyfluorescein because of its exceptional photostability and fluorescence insensitivity to pH change (4-9).

UOM: 1 * 5 mg

Catalog Number: (APOSBICL200-100MG)

Supplier: APOLLO SCIENTIFIC

Description: Primary amine and Sulphhydryl reactive.Enzyme antibody conjugation - Spacer arm.

UOM: 1 * 100 mg

Catalog Number: (APOSBICL202-100MG)

Supplier: APOLLO SCIENTIFIC

Description: Primary amine reactive -Sulphhydryl reactive. Protein conjugation Hapten carrier Protein conjugation

UOM: 1 * 100 mg

Catalog Number: (90001.)

Supplier: Biotium

Description: 5-(and-6)-Carboxyrhodamine 110, SE (5-(and-6)-Carboxyrhodamine 110, succinimidyl ester, mixed isomers), also known as Carboxyrhodamine 110-NHS, is a superior green fluorescent dye that readily reacts with primary or secondary amines. For many applications, the dye is preferred over 5-(and-6)-carboxyfluorescein succinimidyl ester (5(6)-FAM) or FITC because of its exceptional photostability and fluorescence insensitivity to pH (4-9).

UOM: 1 * 5 mg

Catalog Number: (APOSBICL204-100MG)

Supplier: APOLLO SCIENTIFIC

Description: Primary amine and Sulphhydryl reactiveEnzyme antibody conjugation

UOM: 1 * 100 mg

Catalog Number: (40074.)

Supplier: Biotium

Description: The amine reactive succinimidyl ester of green fluorescent AO (acridine orange) can be conjugated to peptides, proteins, drugs, polymeric materials and biomolecules with primary amine groups. The conjugates then are able to complex with nucleic acids, resulting in green fluorescence nucleic acid conjugate adduct, making them potentially useful for studies of nucleic acid binding to various biomolecules, such as DNA-binding proteins.

UOM: 1 * 5 mg

Catalog Number: (90023.)

Supplier: Biotium

Description: 6-FAM, SE (full name: 6-Carboxyfluorescein, succinimidyl ester, single isomer) is the amine-reactive form of 6-carboxyfluorescein single isomer.
6-FAM SE is an amine-reactive green fluorescent dye widely used for labeling oligonucleotides or other biomolecules that contain a primary or secondary aliphatic amine. The coupling reaction is usually carried out at pH 8-9.5.

UOM: 1 * 10 mg

Catalog Number: (90037.)

Supplier: Biotium

Description: 6-ROX, SE (6-Carboxy-X-rhodamine, succinimidyl ester, single isomer) is the amine-reactive form of 6-carboxy-X-rhodamine single isomer.

UOM: 1 * 5 mg

Supplier: MP Biomedicals

Description: p-Nitrophenyl Acetate used with iodoacetic acid for reductive cleavage of methionine-containing peptides. It is also used as a substrate that has been used in assays for esterase and lipase activity. Inorganic complexes have been evaluated for their methanolysis or hydrolysis activity using p-nitrophenyl acetate.