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Key Documents

G1277

Sigma-Aldrich

Glass beads, acid-washed

212-300 μm (50-70 U.S. sieve)

Synonyme(s) :

Glass beads

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About This Item

Code UNSPSC :
41102422
Nomenclature NACRES :
NB.22

Taille des particules

212-300 μm (50-70 U.S. sieve)

Application

Acid-washed glass beads have been used:
  • for the extraction of nucleic acids from pathogens
  • for the preparation of Yarrowialipolytica cell extracts
  • in chromatin immunoprecipitation assay of rat aorta tissues

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Thomas Dubois et al.
mBio, 11(4) (2020-08-21)
The crust is the outermost spore layer of most Bacillus strains devoid of an exosporium. This outermost layer, composed of both proteins and carbohydrates, plays a major role in the adhesion and spreading of spores into the environment. Recent studies
Christopher N Acconcia et al.
Physics in medicine and biology, 62(18), L31-L40 (2017-08-09)
It is well established that high intensity focused ultrasound can be used to disintegrate clots. This approach has the potential to rapidly and noninvasively resolve clot causing occlusions in cardiovascular diseases such as deep vein thrombosis (DVT). However, lack of
Valeria Di Dato et al.
Scientific reports, 10(1), 5374-5374 (2020-03-28)
Prostaglandins (PGs) are hormone-like mediators in many physiological and pathological processes that are present in all vertebrates, in some terrestrial and aquatic invertebrates, and have also been identified in some macroalgae. They have recently been reported also in marine microalgae
Increased expression of CCAAT/enhancer binding protein-? and -? and monocyte chemoattractant protein-1 genes in aortas from hyperinsulinaemic rats
Sato Y, et al.
Diabetologia, 50, 481?489-481?489 (2007)
Jack Paar et al.
Journal of microbiological methods, 112, 28-35 (2015-03-10)
A method, incorporating recently improved reverse transcriptase-PCR primer/probe assays and including controls for detecting interferences in RNA recovery and analysis, was developed for the direct, culture-independent detection of genetic markers from FRNA coliphage genogroups I, II & IV in water

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