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Merck

A1720

Sigma-Aldrich

G 418 二硫酸盐

powder, non-animal origin, suitable for cell culture, BioReagent

别名:

抗生素G418

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About This Item

经验公式(希尔记法):
C20H40N4O10 · 2H2SO4
分子量:
692.71
MDL號碼:
分類程式碼代碼:
12352207
PubChem物質ID:
NACRES:
NA.76

product name

G 418 二硫酸盐, powder, BioReagent, suitable for cell culture

產品線

BioReagent

形狀

powder

光學活性

[α]/D (Specific Rotation: +104.4o (c=0.3% in H2O at 26oC))

效力

≥720 μg per mg (Dried basis)

分子量

692.7

包裝

pkg of 1 g
pkg of 25 g
pkg of 5 g

技術

cell culture | mammalian: suitable

顏色

white to off-white

溶解度

H2O: 100 mg/mL (As a stock solution. Stock solutions should be stored at 2-8°C. Stable at 37°C for 8 days.)

抗生素活性譜

Gram-negative bacteria

作用方式

protein synthesis | interferes

儲存溫度

2-8°C

SMILES 字串

OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](OC[C@@]1(C)O)O[C@H]2[C@H](N)C[C@H](N)[C@@H](O[C@H]3O[C@H]([C@H](C)O)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O

InChI

1S/C20H40N4O10.2H2O4S/c1-6(25)14-11(27)10(26)9(23)18(32-14)33-15-7(21)4-8(22)16(12(15)28)34-19-13(29)17(24-3)20(2,30)5-31-19;2*1-5(2,3)4/h6-19,24-30H,4-5,21-23H2,1-3H3;2*(H2,1,2,3,4)/t6?,7-,8+,9+,10+,11-,12-,13-,14+,15+,16-,17-,18+,19-,20+;;/m0../s1

InChI 密鑰

UHEPSJJJMTWUCP-NKCAIAFTSA-N

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一般說明

G-418是一种由小单孢菌NRRL 5326菌株产生的氨基糖苷类抗生素。它在体内体外均具有光谱的抗菌活性。它还显示出对原生动物、盲肠阿米巴虫和蠕虫的活性。它通常作为遗传霉素选择性抗生素而被人们所熟知。
化学结构:氨基糖苷类

應用

G418二硫酸盐是一种氨基糖苷类抗生素,结构与庆大霉素相似,可用于筛选和维持利用iNOS启动子构建体以及新霉素抗性基因转染的原核和真核细胞†。不同细胞系具有不同的筛选和维持最佳浓度。 细菌和藻类最多需要5 μg/mL而动物细胞则可能需要300-500 μg/mL。

生化/生理作用

G-418对于蛋白合成的抑制是在延伸的早期阶段、起始后、翻译起始阶段以及翻译将要起始的阶段之前。

注意

该产品可2-8°C稳定储存两年。储备溶液可37°C稳定储存8天。

準備報告

G418粉末可以100 mg/mL溶于水。

其他說明

保持容器密闭并置于干燥通风处。置于干燥处。

象形圖

Health hazard

訊號詞

Danger

危險聲明

危險分類

Resp. Sens. 1 - Skin Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Serene R Lai et al.
Methods in molecular biology (Clifton, N.J.), 405, 31-37 (2008-03-29)
RNA interference (RNAi) is one of the most commonly used procedures for gene targeting in today's cutting edge technology and has great potential for use in clinical therapy. Using a plasmid construct that exogenously expresses short-hairpin RNAs (shRNAs) targeting a
G H Wagman et al.
Antimicrobial agents and chemotherapy, 6(2), 144-149 (1974-08-01)
Antibiotic G-418 is a new aminoglycoside produced as the major component by a new species of Micromonospora, M. rhodorangea NRRL 5326. The antibiotic is prepared by submerged fermentation in a soybean-dextrin medium. Antibiotic G-418 is adsorbed on a cationic-exchange resin
D C Eustice et al.
Antimicrobial agents and chemotherapy, 26(1), 53-60 (1984-07-01)
Tetrahymena thermophila is a eucaryotic organism that is highly susceptible to growth inhibition by aminoglycoside antibiotics. Concentrations of paromomycin, gentamicin G418, and hygromycin B at 22, 10, and 17 microM, respectively, inhibited growth by 50%. A combination of in vitro
Hillary C Valley et al.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 18(4), 476-483 (2018-12-20)
Assessment of approved drugs and developmental drug candidates for rare cystic fibrosis (CF)-causing variants of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) requires abundant material from relevant models. Isogenic cell lines harboring CFTR variants in the native genomic context were
Nikolay P Kandul et al.
Nature communications, 11(1), 2106-2106 (2020-05-02)
Here, we describe a drug-inducible genetic system for insect sex-separation that demonstrates proof-of-principle for positive sex selection in D. melanogaster. The system exploits the toxicity of commonly used broad-spectrum antibiotics geneticin and puromycin to kill the non-rescued sex. Sex-specific rescue

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