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G9268

Glass beads, unwashed

425-600 μm (30-40 U.S. sieve)

Synonym(s):

Glass beads

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About This Item

UNSPSC Code:
41100000
NACRES:
NB.22

particle size

425-600 μm (30-40 U.S. sieve)

Application

Unwashedglass beads have been used:

  • in the quantification of protein in fungal colonybiofilm
  • in the lysis of microglial cells for the extraction andquantification of chlorophylls and cell mortality rate
  • in the extraction ofDNA and RNA from microbial communities

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ruoyun Li et al.
Journal of proteomics, 203, 103377-103377 (2019-05-19)
The molecular mechanism of Saccharomyces cerevisiae tolerant to ethanol stress remains to be further elucidated. In this study, a comprehensive analysis based on RNA-seq and iTRAQ LC-MS/MS was used to investigate the global mechanism of S. cerevisiae strain Sc131 in
Production of long chain omega-3 fatty acids and carotenoids in tropical areas by a new heat-tolerant microalga Tetraselmis sp. DS3
Hsin P T, et al.
Food Chemistry, 682-690 (2016)
Daniel R Leadbeater et al.
Microbiome, 9(1), 48-48 (2021-02-19)
Salt marshes are major natural repositories of sequestered organic carbon with high burial rates of organic matter, produced by highly productive native flora. Accumulated carbon predominantly exists as lignocellulose which is metabolised by communities of functionally diverse microbes. However, the
Zinc oxide nanoparticles hinder fungal biofilm development in an ancient Egyptian tomb
Gambino M, et al.
International Biodeterioration & Biodegradation, 122, 92-99 (2017)
Xavier Garcia-Ortega et al.
Frontiers in bioengineering and biotechnology, 3, 107-107 (2015-08-19)
The most commonly used cell disruption procedures may present lack of reproducibility, which introduces significant errors in the quantification of intracellular components. In this work, an approach consisting in the definition of an overall key performance indicator (KPI) was implemented

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