50675
Micro particles based on polystyrene
size: 600 nm
Sinónimos:
Latex beads from PS
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About This Item
Productos recomendados
Quality Level
form
aqueous suspension
concentration
10% (solids)
particle size
600 nm std dev ≤0.03 μm
density
1.05 g/cm3
storage temp.
2-8°C
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Application
Micro particles based on polystyrene, 600 nM may be derivatized to generate media for applications such as antibody conjugation and use in immunoagglutination assay development or the stabilization of Pickering emulsions. Polystyrene microparticles are useful as potential biodegradable vaccine adjuvants and drug delivery devices.
Analysis Note
For every lot exact values of particle size and standard deviation are determined with an accuracy of 0.01 μm using a Coulter Multisizer.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Journal of colloid and interface science, 363(1), 307-313 (2011-08-16)
We have studied polydimethylsiloxane (PDMS)-in-1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF(6)]) Pickering emulsions stabilized by polystyrene microparticles with different surface chemistry. Surprisingly, in contrast to the consensus originating from oil/water Pickering emulsions in which the solid particles equilibrate at the oil-water droplet interfaces and
PDA journal of pharmaceutical science and technology, 62(3), 177-190 (2008-07-30)
The objective of this study is to select a multiple-unit sustained-release formulation and to compare it with both commercial immediate and single unit sustained-release capsules and also to determine whether an in vitro-in vivo correlation exists for single- and multiple-
Sensitive Mie scattering immunoagglutination assay of porcine reproductive and respiratory syndrome virus (PRRSV) from lung tissue samples in a microfluidic chip.
J. Virol. Methods, 178, 31-38 (2011)
Proceedings of the National Academy of Sciences of the United States of America, 106(3), 870-875 (2009-01-14)
Many currently used and candidate vaccine adjuvants are particulate in nature, but their mechanism of action is not well understood. Here, we show that particulate adjuvants, including biodegradable poly(lactide-co-glycolide) (PLG) and polystyrene microparticles, dramatically enhance secretion of interleukin-1beta (IL-1beta) by
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