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Merck
CN

K4000

Sigma-Aldrich

卡那霉素 硫酸酯 来源于卡那霉素链霉菌

Animal Component-free

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别名:
卡那霉素 A, 卡那霉素碱 硫酸盐
经验公式(希尔记法):
C18H36N4O11 · H2O4S
CAS号:
分子量:
582.58
EC 号:
MDL编号:
UNSPSC代码:
51101500
PubChem化学物质编号:
NACRES:
NA.76

生物来源

Streptomyces kanamyceticus

质量水平

形式

powder

效能

≥750 μg per mg (dry basis)

储存条件

(Tightly closed. Dry. Keep in a well -ventilated place. Keep locked up or in an area accessible )

颜色

white to off-white

溶解性

H2O: 50 mg/mL, clear, colorless to faintly yellow

抗生素抗菌谱

Gram-negative bacteria
Gram-positive bacteria
mycobacteria
mycoplasma

作用机制

protein synthesis | interferes

SMILES字符串

OS(O)(=O)=O.NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C18H36N4O11.H2O4S/c19-2-6-10(25)12(27)13(28)18(30-6)33-16-5(21)1-4(20)15(14(16)29)32-17-11(26)8(22)9(24)7(3-23)31-17;1-5(2,3)4/h4-18,23-29H,1-3,19-22H2;(H2,1,2,3,4)/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-;/m1./s1

InChI key

OOYGSFOGFJDDHP-KMCOLRRFSA-N

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相关类别

一般描述

Kanamycin Sulfate is a broad spectrum aminoglycoside-antibiotic derived from Streptomyces kanamyceticus.

应用

Kanamycin sulfate is used as an additive in culture media for the isolation of group D streptococci on Kanamycin Esculin Azide Agar and for selection of transformed plant cells containing the neomycin phosphotransferase on a kanamycin-medium. Kanamycin sulfate can also be used as a selection agent for cells transformed with kanamycin B resistance gene. It is recommended for use in cell culture applications at 100 μg/mL. Kanamycin sulfate from Streptomyces kanamyceticus has been used:
  • in the research of bacterial antibiotic resistance
  • in the research on the effect of different antibiotics on bud regeneration

生化/生理作用

作用机制:该产品通过与70S核糖体亚基结合,抑制易位并引起错误编码而起作用。

耐药机制:氨基糖苷类修饰酶(包括乙酰转移酶、磷酸转移酶、核苷酸转移酶)可以改变这种抗生素,阻止其与核糖体相互作用。

抗菌谱:硫酸卡那霉素对革兰氏阴性和革兰氏阳性菌以及支原体有效。

特点和优势

High quality antibiotic suitable for mulitple research applications

制备说明

Kanamycin sulfate is soluble in water at 50 mg/mL, yielding a clear solution. It is practically insoluble in alcohol, acetone, chloroform, ether and ethyl acetate. A 1% solution in water has a pH of 6.5 to 8.5. Sterile solutions can be prepared by a sterile filtration, through a .2μm filter.

Solutions are stable at 37°C for approximately 5 days. Aqueous stock solutions can be stored at 2-8°C for long term storage.

储存及稳定性

Tightly closed. Dry. Keep in a well -ventilated place. Keep locked up or in an area accessible

其他说明

For additional information on our range of Biochemicals, please complete this form.

象形图

Health hazard

警示用语:

Danger

危险声明

危险分类

Repr. 1B

WGK

WGK 2

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

监管及禁止进口产品

分析证书(COA)

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在文件库中查找您最近购买产品的文档。

访问文档库

Didrik H Grevskott et al.
Frontiers in microbiology, 8, 24-24 (2017-02-06)
The mechanisms for the development and spread of antibacterial resistance (ABR) in bacteria residing in environmental compartments, including the marine environment, are far from understood. The objective of this study was to examine the ABR rates in Escherichia coli and
Effect of gelling agents and antibiotics on adventitious bud regeneration from In vitro leaves of pear
Chevreau et al.
In Vitro Cellular & Developmental Biology. Plant, 33, 173?179-173?179 (1997)
J Yuyang Lu et al.
Cell reports, 30(10), 3296-3311 (2020-03-12)
Repetitive elements are abundantly distributed in mammalian genomes. Here, we reveal a striking association between repeat subtypes and gene function. SINE, L1, and low-complexity repeats demarcate distinct functional categories of genes and may dictate the time and level of gene
Benjamin Bardiaux et al.
Structure (London, England : 1993), 27(7), 1082-1093 (2019-05-06)
Bacterial type 4a pili are dynamic surface filaments that promote bacterial adherence, motility, and macromolecular transport. Their genes are highly conserved among enterobacteria and their expression in enterohemorrhagic Escherichia coli (EHEC) promotes adhesion to intestinal epithelia and pro-inflammatory signaling. To
Marta Lukačišinová et al.
Nature communications, 11(1), 3105-3105 (2020-06-21)
Genetic perturbations that affect bacterial resistance to antibiotics have been characterized genome-wide, but how do such perturbations interact with subsequent evolutionary adaptation to the drug? Here, we show that strong epistasis between resistance mutations and systematically identified genes can be

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