AMCA-H

CHF 61.00
In stock
CDX-A0009-M100100 mgCHF 61.00
CDX-A0009-M500500 mgCHF 191.00
CDX-A0009-G0022 gCHF 575.00
More Information
Product Details
Synonyms 7-Amino-4-methyl-3-coumarinylacetic acid
Product Type Chemical
Properties
Formula

C12H11NO4

MW 233.22
CAS 106562-32-7
Source/Host Chemicals Synthetic.
Purity Chemicals ≥90% (HPLC)
Appearance Brown solid.
Solubility Soluble in DMSO or DMF.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key QEQDLKUMPUDNPG-UHFFFAOYSA-N
Smiles CC1=C(CC(O)=O)C(=O)OC2=C1C=CC(N)=C2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF

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 Stoke's 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.

Product References

(1) G-L. Ferri et al.; J. Histochem. Cytochem. 45(2), 155 (1997) | (2) B. Ufhake et al.; J. Neurosc. Meth. 40(1), 39 (1991) | (3) M. W. Wessendorf et al.; J. Histochem. Cytochem. 38(1), 87 (1990)

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