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Eu-W1024 labeled Protein G is for LANCE® assays where the analyte concentration is < 1-10 nmol/L and assay pH > 7. Protein G is a recombinant form cloned from Streptococcus spp. and produced in E. coli. Protein G binds to the Fc region of IgG by a non-immune mechanism which is similar to that of Protein A, but the binding range is broader and the binding affinity greater for Protein G. Protein G binds to all subclasses of human IgG and mouse IgG. In addition it binds to rat, goat, sheep, guinea pig, rabbit, cow, pig and horse antibodies. It does not bind to chicken or cat antibodies, and binds weakly to IgG from dog. Protein G does not bind to human IgA, IgM or serum albumin. Protein G is supplied ready for use in 50 mmol/L Tris HCl buffered saline solution. As a general guideline for DELFIA® immunoassays, a final concentration of 100 ng/mL Protein G may be suitable for generation of the assay signal.
Eu-labeled protein G has also been used successfully in a LANCE™ receptor binding assay. In this assay, an Fc-fusion protein was bound to a biotinylated ligand, with APC-labelled streptavidin at the same concentration as the ligand as the acceptor. The Eu-labelled protein concentration was twice that of the receptor. In this assay, a signal-to-noise ratio of 8.5 was observed, which was similar to that seen when using Eu-labelled protein A in the same assay.
Generic LANCE® reagents are intended for setting up homogeneous time-resolved fluorescence resonance energy transfer (TR-FRET) based assays using Eu-Chelate label as a donor and APC-labeled reagent as an acceptor. Generic reagents facilitate setting up LANCE® assays when there is a limited amount of specific reagents available or the assay reagents are relatively unstable. To enable optimization of both the signal or the noise ratio and signal stability, some of the generic reagents are labeled with two different chelates, W1024 or W8044.
LANCE® (Lanthanide chelate excite) and LANCE® Ultra are our TR-FRET (time-resolved fluorescence resonance energy transfer), homogeneous (no wash) technologies. One molecule of interest is labeled with a donor fluorophore (a LANCE Europium chelate) and the second molecule is labeled with an acceptor fluorophore [ULight™ dye, allophycocyanin (APC), etc.]. Upon excitation at 320 or 340 nm, energy can be transferred from the donor Europium chelate to the acceptor fluorophore if sufficiently close for FRET (~10 nm). This results in the emission of light at 665 nm (for ULight dye and APC).
|Antibody Conjugates||Protein G|
|Detection Method||Time-Resolved Fluorescence (TRF), TR-FRET|
|Experimental Type||In vitro|
|Product Brand Name||LANCE|
|Shipping Condition||Dry Ice|
|Unit Size||10 µg|
The introduction of enzyme-linked immunosorbent assays (ELISAs) in the early 1970’s offered researchers a non-radiometric immunoassay platform without compromising sensitivity. Over the last 50 years scientists have made huge strides in disease research and drug discovery and a demand for greater assay throughput and sensitivity has evolved. In response, more robust immunoassays have been developed to address some of the limitations of the standard, colorimetric ELISA.
Find out about the most common limitations of traditional ELISAs and how different ELISA alternative technologies address these limitations.
Generic LANCE reagents are intended for setting up TR-FRET based assays using Eu-chelate label as a donor and APC-labeled reagent as an acceptor.