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B6385

Sigma-Aldrich

Benzoylated Naphthoylated DEAE–Cellulose

medium

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About This Item

MDL number:
MFCD00146160
UNSPSC Code:
47101511
NACRES:
NA.56

form

powder

Quality Level

200

particle size

, medium

storage temp.

2-8°C

Application

Benzoylated Naphthoylated DEAE-cellulose is a cellulose medium used in protein chromatography, ion exchange chromatography and anion exchange media. Benzoylated Naphthoylated DEAE is particularly useful for the separation of single and double stranded DNA. Benzoylated Naphthoylated DEAE has been used to design a more efficient approach for the detection of human papillomavirus DNA and to study the cytotoxcity of the drug 5-Fluorouracil (FUra).

Preparation Note

Prepared by the method of Gillam et al., Biochemistry, 6, 3043 (1967).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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J D Schuetz et al.
Cancer chemotherapy and pharmacology, 21(3), 208-210 (1988-01-01)
5-Fluorouracil (FUra) was previously demonstrated to be incorporated into DNA at cytotoxic concentrations in mouse bone marrow cells. Subsequently, we showed that under these conditions FUra exhibited a time-dependent removal from DNA accompanied by a decrease in DNA strand length.
R M Knobler et al.
Clinical and experimental dermatology, 17(6), 392-396 (1992-11-01)
Using the benzoylated naphthoylated DEAE cellulose method (BND-method) we have designed a more efficient approach for the detection of human papillomavirus-DNA (HPV-DNA) via dot-blot and hybridization. Biopsy material from anogenital warts (40 patients), invasive carcinoma uteri (12 patients) and normal
A N Koterov et al.
Biokhimiia (Moscow, Russia), 57(2), 195-200 (1992-02-01)
Single-stranded DNA-binding proteins (SSB-proteins) isolated from Ehrlich ascites tumour (EAT) cells were incubated for 30 min at 5 mM NaCl with salmon sperm DNA or [3H]DNA from EAT at the SSB-protein/DNA ratio (w/w) of 0 to 4.5. After addition of
Ana Teixeira-Silva et al.
Nature communications, 8(1), 1982-1982 (2017-12-08)
Replication requires homologous recombination (HR) to stabilize and restart terminally arrested forks. HR-mediated fork processing requires single stranded DNA (ssDNA) gaps and not necessarily double strand breaks. We used genetic and molecular assays to investigate fork-resection and restart at dysfunctional
Bo-Ruei Chen et al.
The Journal of cell biology, 218(7), 2113-2123 (2019-05-28)
XRCC4-like factor (XLF) is a non-homologous end joining (NHEJ) DNA double strand break repair protein. However, XLF deficiency leads to phenotypes in mice and humans that are not necessarily consistent with an isolated defect in NHEJ. Here we show that
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