MBD0055
MediaBoost
non-animal sterile microbial growth supplement
Sinónimos:
growth supplement for germination, microbial culture additive, microbial culture enhancer, microbial media supplement, minimal growth media supplement
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About This Item
Código UNSPSC:
41106212
NACRES:
NB.21
Productos recomendados
Nivel de calidad
esterilidad
sterile
Formulario
liquid
técnicas
microbiological culture: suitable
Condiciones de envío
wet ice
temp. de almacenamiento
2-8°C
idoneidad
Bacillus spp.
Escherichia spp.
Lactobacillus spp.
Lactococcus spp.
Pseudomonas spp.
Saccharomyces spp.
bacteria
yeasts
Descripción general
Studying microbial species via cutting edge genomic techniques such as next generation sequencing (NGS) has become increasingly prevalent in recent years; however, genomic methods alone cannot fully replace experimental testing of microbial species. Therefore, the ability to culture microbes in a laboratory setting remains essential for comprehensive study of these communities. Some microbial species can be challenging to culture in standard culture media. Often species of interest or a specific process require specialized media compositions, to provide an optimal environment for maximal proliferation and yield. A few examples includes
- Chemically defined minimal growth media are often used to grow bacteria for proteomics, as a base for stable isotope enrichment in NMR protein structure-function studies, but growth can be limited without the addition of an effective supplement.
- Use of chemically defined minimal growth media in the production of secreted microbial proteins to ensure reproducibility and a higher concentration of the microbial-produced protein of interest.
Aplicación
MediaBoost provides microbial researchers a ready-to-use media supplement to amplify growth in selected gram-positive bacteria, gram-negative bacteria, and yeast species. Application data is available for some of the strains and media combinations that have been tested with MediaBoost, including:
Please note strains and media combinations and should be tested on a case-by-case basis by the researcher for experiment optimization.
- Bacillus subtilis spores in LB medium
- Lactobacillus rhamnosus in LB medium
- Pseudomonas aeruginosa in M9 medium
- Saccharomyces cerevisiae in YPD, BM2, and IMDM media
Please note strains and media combinations and should be tested on a case-by-case basis by the researcher for experiment optimization.
Características y beneficios
- Boosts Growth of Certain Microorganisms
- Reduces Germination Time
- Ready-Made, Sterile Solution
- Protein-Free
Producto relacionado
Referencia del producto
Descripción
Precios
Código de clase de almacenamiento
12 - Non Combustible Liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Anna Gąciarz et al.
Microbial cell factories, 16(1), 108-108 (2017-06-18)
The production of recombinant proteins containing disulfide bonds in Escherichia coli is challenging. In most cases the protein of interest needs to be either targeted to the oxidizing periplasm or expressed in the cytoplasm in the form of inclusion bodies
M Bonnet et al.
New microbes and new infections, 34, 100622-100622 (2020-01-21)
Microbiology has been largely developed thanks to the discovery and optimization of culture media. The first liquid artificial culture medium was created by Louis Pasteur in 1860. Previously, bacterial growth on daily materials such as some foods had been observed.
Maryam Tidjani Alou et al.
Clinical microbiology reviews, 34(1) (2020-10-30)
The last 5 years have seen a turning point in the study of the gut microbiota with a rebirth of culture-dependent approaches to study the gut microbiota. High-throughput methods have been developed to study bacterial diversity with culture conditions aimed
Stephan B Azatian et al.
Journal of biomolecular NMR, 73(1-2), 11-17 (2019-01-08)
We describe a general and simple modification to the standard M9 minimal medium recipe that leads to an approximate twofold increase in the yield of heterologously expressed proteins in Escherichia coli BL21(DE3) bacteria. We monitored the growth of bacteria transformed
Chandar S Thakur et al.
Applied microbiology and biotechnology, 88(3), 771-779 (2010-08-24)
Since RNAs lie at the center of most cellular processes, there is a need for synthesizing large amounts of RNAs made from stable isotope-labeled nucleotides to advance the study of their structure and dynamics by nuclear magnetic resonance (NMR) spectroscopy.
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