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Merck
CN

C3145

Cellulose phosphate

fibers, 50-150 μm

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About This Item

CAS Number:
UNSPSC Code:
47101511
MDL number:
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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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Atanaska V Mitkova et al.
Biochemistry, 41(16), 5255-5265 (2002-04-17)
Plasmid DNA replication in nuclear extracts of Saccharomyces cerevisiae in vitro has been shown to be S-phase specific, similar to that observed in vivo. We report here a reconstituted in vitro system with partially purified replication proteins, purified replication protein
Yaşar Demir et al.
Preparative biochemistry & biotechnology, 33(4), 311-320 (2003-11-11)
In this research, acid phosphatase was purified and characterized from approximately 3000-year-old human bones from archeological excavations. Using anion exchange chromatography, two isoenzymes, TrACP and TsACP, were isolated from the bone. TrACP and TsACP were eluted separately, with a concentration
Takahiko Taguchi et al.
Cell biochemistry and function, 20(3), 213-221 (2002-07-19)
Putrescine biosynthesis is elevated before DNA replication, and a stimulation of DNA synthesis by 20 mM putrescine has been found using an in vitro DNA synthesizing system. Furthermore, this stimulation of DNA synthesis by putrescine involves a particular factor (factor
Mariana Yaneva et al.
Methods in molecular biology (Clifton, N.J.), 338, 291-303 (2006-08-05)
A subset of the proteome that binds to specific DNA sequences is at the center of genome function, integrity, and dynamics. We present a detailed protocol that allows the isolation of any specific DNA binding protein and its subsequent identification
A N Carter
Current protocols in molecular biology, Chapter 18, Unit 18-Unit 18 (2008-02-12)
In studies of the regulation of specific biochemical events by reversible phosphorylation, assaying the protein kinases themselves can often lead to significant progress in understanding the mechanistic details of a system under study. This unit describes assays for a variety

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