产品名称
5-溴-2′-脱氧尿苷, >97%, crystalline solid, pkg of 1 g
SMILES string
OC[C@H]1O[C@H](C[C@@H]1O)N2C=C(Br)C(=O)NC2=O
InChI
1S/C9H11BrN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1
InChI key
WOVKYSAHUYNSMH-RRKCRQDMSA-N
assay
>97%
form
crystalline solid
mol wt
307.1
packaging
pkg of 1 g
manufacturer/tradename
Roche
mp
191-194 °C (dec.) (lit.)
shipped in
wet ice
storage temp.
2-8°C
Quality Level
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Analysis Note
纯度 :97%(来自 N),色谱均一
Application
5-溴-2′-脱氧尿苷已用于在细胞增殖研究中标记细胞周期S期细胞和原代肝细胞。
可被免疫化学检测到的核苷酸,可代替胸苷掺入 DNA 中。根据姐妹染色单体交换 (SCE) 方法,用于体内 DNA 合成研究 和致突变物质检测。
Biochem/physiol Actions
用作遗传研究中诱变剂的胸苷类似物。在 S 期可选择性结合到细胞 DNA 中。
General description
通常用作 DNA 的 S 期合成的标记物。
Other Notes
仅用于生命科学研究。不可用于诊断。
Preparation Note
工作浓度: 据文献报道用于细胞培养,终浓度为 10μmol/l。
据文献报道,5~50 mg/kg 体重小鼠已用于细胞增殖的检测。
工作溶液的制备
对应于 Roche 细胞增殖 ELISA、BrdU 试剂盒和 Roche 5-溴-2′ 中包含的 BrdU 标记试剂-脱氧尿苷标记和检测试剂盒,将物质溶于 PBS 中,制备 BrdU 工作液至 10 mM 储备液(BrdU 的分子量 = 307.1 D)。对于 体内 使用, BrdU 溶解在 PBS 中;对于 体外 BrdU 的使用,溶于双蒸水中,浓度与 10 mM 相同。
储存条件(工作液):-15 至-25°C
据文献报道,5~50 mg/kg 体重小鼠已用于细胞增殖的检测。
工作溶液的制备
对应于 Roche 细胞增殖 ELISA、BrdU 试剂盒和 Roche 5-溴-2′ 中包含的 BrdU 标记试剂-脱氧尿苷标记和检测试剂盒,将物质溶于 PBS 中,制备 BrdU 工作液至 10 mM 储备液(BrdU 的分子量 = 307.1 D)。对于 体内 使用, BrdU 溶解在 PBS 中;对于 体外 BrdU 的使用,溶于双蒸水中,浓度与 10 mM 相同。
储存条件(工作液):-15 至-25°C
signalword
Danger
hcodes
Hazard Classifications
Muta. 1B - Repr. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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American journal of physiology. Cell physiology, 285(2), C253-C259 (2003-04-04)
The present study was designed to develop methods to study the production and release of monocytes from the bone marrow using the thymidine analog 5'-bromo-2'-deoxyuridine (BrdU). Dividing monocytes in bone marrow were labeled with BrdU (MOBrdU), and their release into
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Proliferating cell nuclear antigen (PCNA) was evaluated as a marker of cell proliferation in formalin-fixed rat liver tissue through a comparative study with the thymidine analogue 5-bromo-2'-deoxyuridine (BrdU). The comparison was conducted through the introduction of a dual immunohistochemical procedure
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