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Merck

10843555001

Roche

潮霉素B

from Streptomyces hygroscopicus

别名:

潮霉素B 来源于吸水链霉菌

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About This Item

经验公式(希尔记法):
C20H37N3O13
CAS号:
分子量:
527.52
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

生物来源

Streptomyces hygroscopicus

无菌性

non-sterile; 0.2 μm filtered

方案

80% (HPLC)

表单

buffered aqueous solution

组成

Hygromycin B, >80% HPLC

包装

pkg of 20 mL (1 g)

制造商/商品名称

Roche

浓度

50 mg/mL

技术

transfection: suitable

SMILES字符串

CN[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@@H]3O[C@]4(O[C@H]([C@H](N)CO)[C@H](O)[C@H](O)[C@H]4O)O[C@H]23)[C@@H]1O

InChI

1S/C20H37N3O13/c1-23-7-2-5(21)9(26)15(10(7)27)33-19-17-16(11(28)8(4-25)32-19)35-20(36-17)18(31)13(30)12(29)14(34-20)6(22)3-24/h5-19,23-31H,2-4,21-22H2,1H3/t5-,6-,7+,8-,9+,10-,11+,12-,13+,14-,15-,16+,17+,18-,19+,20+/m1/s1

InChI key

GRRNUXAQVGOGFE-XKIAHZFYSA-N

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相关类别

一般描述

  • 分子式:C20H37N3O13
  • LD50: 小鼠6 mg/kg(静脉注射);豚鼠13 mg/kg(腹腔注射); 大鼠63 mg/kg (腹腔注射)
  • 分子量:Mr = 527.5
  • 工作浓度:细胞培养中50 - 1,000 μg/ml。用于选择哺乳动物细胞的常用浓度是 200μ g/ml。。但是,最佳浓度必须通过实验确定,因为它可能会因使用的细胞类型而异。

应用

潮霉素 B 是一种氨基糖苷抗生素,可抑制原核生物和真核生物中的蛋白质合成。它被用于选择和维持可以稳定转染大肠杆菌潮霉素抗性基因(hyg 或 hph)的真核细胞的表型。

生化/生理作用

作用机制:本品通过诱导原核生物中m-RNA模板的误读,抑制蛋白质合成,具有抑制翻译的作用。

抗菌谱:潮霉素B对细菌、真菌和高等真核细胞有抑制作用。

质量

纯度:>80%(HPLC)

单位定义

单位试验:Unit/mg
我们没有这些信息。

外形

溶液,50 mg/ml,溶于PBS(磷酸盐缓冲生理盐水 )中,已通过0.2 μm孔径滤膜过滤。

制备说明

工作浓度:在细胞培养中用于选择抗性细胞的推荐浓度是1000μ g/ml。 用于选择哺乳动物细胞的常用浓度是 200μ g/ml。 但是,最佳浓度必须通过实验确定,因为可能会因使用的细胞类型而异。

储存及稳定性

2至8 °C下储存。(溶液)

其他说明

仅用于生命科学研究。不用于诊断操作。
溶液,50 mg/ml,溶于PBS(磷酸盐缓冲生理盐水 )中,已通过0.2 μm孔径滤膜过滤。

警示用语:

Danger

危险分类

Acute Tox. 1 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Eye Dam. 1 - Resp. Sens. 1 - Skin Sens. 1

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 1

闪点(°F)

does not flash

闪点(°C)

does not flash


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yiping Qi et al.
Methods in molecular biology (Clifton, N.J.), 712, 21-30 (2011-03-02)
Plant disease resistance (R) proteins confer strong resistance against pathogens by recognizing particular pathogen effectors. Identification of proteins associated with an R protein will provide insight into the mechanism of R protein function. Many R proteins are associated with the
Wouter Koole et al.
Nucleic acids research, 41(16), e158-e158 (2013-07-19)
Here, we report the investigation of microsatellite instability (MSI) in human cells with a newly developed reporter system based on fluorescence. We composed a vector into which microsatellites of different lengths and nucleotide composition can be introduced between a functional
Charlotte Vandermeulen et al.
PLoS pathogens, 17(9), e1009919-e1009919 (2021-09-21)
Viral infections are known to hijack the transcription and translation of the host cell. However, the extent to which viral proteins coordinate these perturbations remains unclear. Here we used a model system, the human T-cell leukemia virus type 1 (HTLV-1)
Elisa Gobbini et al.
Cell reports, 33(3), 108287-108287 (2020-10-22)
Homologous recombination is initiated by nucleolytic degradation (resection) of DNA double-strand breaks (DSBs). DSB resection is a two-step process in which an initial short-range step is catalyzed by the Mre11-Rad50-Xrs2 (MRX) complex and limited to the vicinity of the DSB
Najma Shaheen et al.
Frontiers in cell and developmental biology, 9, 727972-727972 (2021-10-19)
In metazoans, heritable states of cell type-specific gene expression patterns linked with specialization of various cell types constitute transcriptional cellular memory. Evolutionarily conserved Polycomb group (PcG) and trithorax group (trxG) proteins contribute to the transcriptional cellular memory by maintaining heritable

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