You searched for: Protein Linking and Labeling Systems

Protein linking and labeling systems provide a convenient means for attaching fluorescent labels or biotins to antibodies and larger proteins. These kits are ideal for use with multiple applications, including flow cytometry, fluorescent microscopy, immunohistochemistry, primary detection, ELISAs, immunocytochemistry, and FISH. These systems are available with a variety of dye colors, biotin, fluorescent agents, and all the components needed to perform multiple conjugations and purifications. Protein labeling follows a simple protocol of reaction, separation, and then use.

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Amersham CyDye DIGE fluors

Supplier: Cytiva

CyDye™ DIGE fluors are available as minimal and saturation labeling dyes. The minimal dyes are intended for general 2-D application use where sufficient amounts of sample are available. The saturation dyes from the Scarce Sample Labeling Kit are designed to be used for applications where only small amounts of sample are available, for example in Laser Capture Microdissection.

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Fluorescent dyes, M series, streptavidin conjugate

Supplier: Abnova

Fluorescent dye, M series, products are designed to be maximally excited by one of the major light sources equipped in flow cytometers. In comparison with phycobiliprotein tandems, Fluorescent dye, M series, possesses better photostability, higher conjugation yields, and little pH sensitivity making it an ideal choice in fluorescence imaging applications.

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Peroxidase substrates, TrueBlue™

Supplier: SERACARE LIFE SCIENCES

KPL TrueBlue™ peroxidase substrate is a highly sensitive chromagenic substrate for visualisation of horseradish peroxidase-labeled reporter reagents.

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AlphaLISA® Streptavidin Acceptor Beads, 250 µg

Supplier: PerkinElmer

These beads can be used in conjunction with Alpha Donor beads to create AlphaLISA® no-wash assays for: Protein-protein interaction assays, Protein-DNA interaction assays, Protein-RNA interaction assays, protein-small molecule interaction assays, analyte detection assays, biomarker detection assays, antibody detection assays, enzymatic assays, other immunoassays in a typical AlphaLISA assay, 1 mg of acceptor beads is sufficient to run 1,000 to 2,000 wells using a 50 µl reaction volume.