Lecteur de plaque d'absorbance avec port cuvette
Le lecteur de microplaque d'absorbance innovant de BMG LABTECH a la flexibilité d'effectuer des tests rapidement et facilement dans les microplaques ou via le port de cuvette intégré. Ce lecteur de microplaque d'absorbance à base de spectrophotomètre capture un spectre UV / visible complet en moins de 1 sec / puits. Sa vitesse, son simple bouton-poussoir et sa capacité à stocker des protocoles d'essais individuels font du SPECTROstar® Nano le leader des lecteurs de microplaque pour les mesures d'absorbance.
Le SPECTROstar Nano est équipé du spectrophotomètre UV / vis ultra rapide de BMG LABTECH, qui permet aux utilisateurs de mesurer l'absorbance en spectre complet (220 - 1000 nm) en moins de 1 seconde par puits. C'est l'instrument idéal pour lire tous les tests d'absorbance dans une microplaque ou une cuvette - avec de nombreux protocoles de tests courants prédéfinis et disponibles en cliquant sur la souris.
- Mesures d'absorbance ultra rapides
- Mesures jusqu'aux plaques 1536 puits
- Port cuvette intégré
- Compatibilité plaque LVis
- Incubation jusqu'à 45 °C
- Multiples options d'agitation
- Scanning du puits avec jusqu'à 900 points de données par puits
"One thing to point out is the wonderful ability to run a complete scan and then go in afterwards and select the peak areas and set wavelengths for analysis. We would not have seen the unique spectral shift in our dye-end point water hardness method using our older single wavelength instrument. The SPECTROstar Nano is making work and life easier, more unique and more interesting for us."
Gary Spedding, Brewing and Distilling Analytical Services, USA
Assay development for essential enzyme activity in the tegument of live SchistosomesMadhu Sundaraneedi1 , Luke Becker2 , Giovanni Abbenante3 , Alex Loukas2 , Grant Collins1 , Mark Pearson2, 1School of Physical, Environmental and Mathematical Sciences, University of New South Wales, Australia , 2Australian Institute for Tropical Health and Medicine, James Cook University, Australia , 3BMG LABTECH Australia, 12/2017
Schistosomiasis is a parasitic disease that affects over 200 million people in tropical, developing nations, causing severe morbidity and over 300,000 deaths annually. Schistosomiasis is treated with a single drug and no vaccine is available.
We selected three Schistosoma surface-associated enzymes that are indispensable to parasitic survival: alkaline phosphatase; phosphodiesterase SmNPP-5 and an acetylcholinesterase. The activity of these molecules on the surface of live and intact larval and adult Schistosoma can be assayed in real-time of cultured parasites, providing a tool to assess the efficacy of drugs or vaccines targeting these enzymes. The colorimetric assay was read on a FLUOstar® Omega microplate reader.
The versatile instrument supports development of assays and drugs. Apart from its absorbance spectrometer, the FLUOstar Omega is equipped with fluorescence and luminescence detection capabilities allowing fast and reliable endpoint and kinetic measurements in all detection modes.
Detection of plant-synthesized nanoparticles and their antibacterial capacitySalem W. and Schild S., University of Graz , Institute of Molecular Biosciences , BioTechMed-Graz , Austria, 03/2017
Metallic nanoparticles became subject of intensive research because of their potential antibiotic properties. Nanoparticles such as silver, gold or zinc oxide particles are easily and cost-effectively synthesized by blending metal salts with plant extracts that reduce the metal. Different extracts, varying in the plant or the part of the plant used for the extract, are currently investigated in regard to their capacity to form nanoparticles and their antimicrobial efficacy. The formation of nanoparticles can be verified by UV-Vis spectroscopy due to surface plasmon resonance of the particles that lead to a characteristic spectrum defined by the underlying metal and particle size. Subsequent analysis of nanoparticles on microbial growth is typically tested by methods based on absorbance changes.
Here, we present how the spectrometer-based BMG LABTECH instruments are used to quickly confirm Ag and ZnO nanoparticle formation and their inhibitory effect on the diarrhea-causing bacteria Vibrio cholerae and enterotoxic Escherichia coli (ETEC).
Absorbance-based methods for protein quantification on BMG LABTECH instrumentsAndrea Krumm, BMG LABTECH, 09/2016
Measuring the protein concentration of liquid samples is a routine analysis in many life science laboratories. Accurate quantification is often a critical step for subsequent analyses such as protein characterization or western blots. Absorbance-based methods are well-established, easy to handle and cheap. They can be performed in microplates, allowing for high sample numbers processed at a time and low reagent volumes.
Spectrometer-based BMG LABTECH readers capture absorbance spectra or absorbance at discrete wavelengths from 220-1000 nm in less than a second per well and therefore can easily read these assays. The most common methods absorbance at 280 nm, Bradford, Bicin-Choninic Acid (BCA) and Lowry assay are presented here.
ProteaseTag active NE immunoassay: a rapid test to quantify neutrophil elastase levels in patientsOliver Carney (1) , Kelly Moffitt (2) , Charlene Robb (2), 1) BMG LABTECH , 2) ProAxsis, 02/2016
The neutrophil elastase is a biomarker of respiratory diseases such as cystic fibrosis (CF) or chronic obstructive pulmonary disease (COPD). A simple, rapid and accurate test for neutrophil elastase levels in patient samples would be a significant medical benefit. Established methods do not specifically verify the presence of the enzyme leading to a high value of false positives. In this application note we show how to use the ProteaseTag™ Active Neutrophil Elastase Immunoassay from the company ProAxsis which is based in Northern Ireland.
The assay uses tags to specifically bind the enzyme of interest. Chromogenic detection is performed with the CLARIOstar® microplate reader which analysis the results and return qualified data automatically.
Protease levels can be determined in sputum sol, bronchoalveolar lavage, wound exudate or serum free cell culture.
Authentication and quality testing of distilled spirits using the SPECTROstar NanoGary Spedding (1) , Carl Peters (2), 1) Brewing and Distilling Analytical Services LLC , 2) BMG LABTECH, 01/2015
Alcoholic beverages that are produced by distillation are called distilled beverages. Some known distilled beverages include vodka, gin, tequila, rum, and whisky. Beer, wine, and cider are excluded from this category as these are fermented but not distilled.
The distilled beverages industry is expanding, indicated by the constant release of new products. On the other hand, counterfeiters as well as cases of adulteration and dilution of distilled spirits and liqueurs are also on the increase. It would be of great advantage to find an easy way to test distilled spirits for authentication.
One possible method is to take UV-Vis absorbance spectra from the liquid samples. Recently, it was shown in literature that these spectra work as brand "fingerprints". There is, for example, a clear difference between a whiskey that has aged in wood compared to an unaged whiskey.
A convenient way to measure UV-Vis absorbance spectra and to perform a quality control check is achieved by using the SPECTROstar® Nano. This microplate and cuvette reader offers rapid and efficient spectral analysis measurements. The associated MARS Data Analysis Software stores all spectral data in a way that the creation of specific spirit fingerprint libraries is possible.