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Chemical Structure
Chemical Structure
Chemical Structure

AMCA-H [106562-32-7]

Research Use Only
CDX-A0009
Chemodex
CAS Number106562-32-7
Product group Chemicals
Estimated Purity>90%
Molecular Weight233.22
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    AMCA-H [106562-32-7]
  • Delivery Days Customer
    10
  • CAS Number
    106562-32-7
  • Certification
    Research Use Only
  • Estimated Purity
    >90%
  • Hazard Information
    Non-hazardous,Warning
  • Molecular Formula
    C12H11NO4
  • Molecular Weight
    233.22
  • Scientific Description
    AMCA is one of the brightest amine-reactive blue fluorescent dyes useful for immunofluorescence and fluorescent labeling (Ex/Em: 353/455nm). It is quite photostable, and its fluorescence is pH-independent from pH 4 to 10. The properties include a relatively large Stokes shift and resistance to photobleaching. Reactive AMCA derivatives are used as contrasting probes for double and triple labeling in immunofluorescence microscopy, arrays and in situ hybridization. NHS-AMCA and Sulfo-NHS-AMCA are reactive towards primary amine groups on antibodies, proteins, peptides and other biomolecules. AMCA-Hydrazide is used to label glycosylation sites or for conjugation to carboxyl groups using the crosslinker EDC. - Chemical. CAS: 106562-32-7. Formula: C12H11NO4. MW: 233.22. Synthetic. AMCA is one of the brightest amine-reactive blue fluorescent dyes useful for immunofluorescence and fluorescent labeling (Ex/Em: 353/455nm). It is quite photostable, and its fluorescence is pH-independent from pH 4 to 10. The properties include a relatively large Stokes shift and resistance to photobleaching. Reactive AMCA derivatives are used as contrasting probes for double and triple labeling in immunofluorescence microscopy, arrays and in situ hybridization. NHS-AMCA and Sulfo-NHS-AMCA are reactive towards primary amine groups on antibodies, proteins, peptides and other biomolecules. AMCA-Hydrazide is used to label glycosylation sites or for conjugation to carboxyl groups using the crosslinker EDC.
  • SMILES
    CC1=C(CC(O)=O)C(=O)OC2=C1C=CC(N)=C2
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200