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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).
調製ノート
Gillam et al.(Biochemistry, 6, 3043 (1967))の方法で調製されています。
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
B6385-5G:
B6385-10G:
B6385-50G:
B6385-25G:
B6385-VAR:
B6385-100G:
B6385-BULK:
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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