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form
fibers
particle size
50-150 μm
capacity
~3.8 meq/g
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Application
Cellulose phosphate is used in protein chromatography, ion exchange chromatography and cation exchange media. Cellulose phosphate (CELLPHOS) has been studied as a collector for analytical preconcentration of traces of Cd(II), Cr(III), Cu(II) and Ni(II) from aqueous sample solution and used to purify and characterize acid phosphatase from approximately 3000-year-old human bones from archeological excavations.
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
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Nadine Pelletier et al.
Current protocols in protein science, Chapter 14, Unit 14-Unit 14 (2008-11-20)
Protein lysine acetylation, referring to acetylation of the epsilon-amino group of a lysine residue, has recently emerged as an important post-translational modification for regulating protein functions in various organisms. Like phosphorylation, lysine acetylation is a rapidly reversible and precisely controlled
Histone octamer trans-transfer: a signature mechanism of ATP-dependent chromatin remodelling unravelled in wheat nuclear extract.
Raut, V.V., et al.
Annals of Botany, 108, 1234-1246 (2011)
Nikita Avvakumov et al.
The Journal of general virology, 83(Pt 3), 517-524 (2002-02-14)
Adenovirus type 5 E1A proteins interact with cellular regulators of transcription to reprogram gene expression in the infected or transformed cell. Although E1A also interacts with DNA directly in vitro, it is not clear how this relates to its function
Preparation of microtubule protein and purified tubulin from bovine brain by cycles of assembly and disassembly and phosphocellulose chromatography.
Herbert P Miller et al.
Methods in cell biology, 95, 3-15 (2010-05-15)
Stefan Söllner et al.
Extremophiles : life under extreme conditions, 10(6), 629-634 (2006-08-10)
A restriction endonuclease activity from Sulfolobus islandicus REN2H1 was purified by phosphocellulose and cation exchange chromatography. The enzyme cuts DNA at the recognition site GCwGC as could be shown by restriction analysis of plasmids and short synthetic duplex DNA. The
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