Neomycin Sulfate
Neomycin Sulfate
Gibco™

Neomycin Sulfate

Gibco™ネオマイシンは、ストレプトマイセスフラジエによって生成されます。ポリミキシンB硫酸塩は、細菌リボソームの30Sサブユニットに結合することで作用し、タンパク質の合成および感受性細菌の死亡を阻害します。Gibco™ネオマイシン硫酸塩は、細胞培養における細菌汚染の防止に使用されます。この抗生物質はグラム陰性細菌に対して高い活性を示します。推奨される使用濃度は50 µg/mlです詳細を見る
製品番号(カタログ番号)数量
21810031100 g
製品番号(カタログ番号) 21810031
価格(JPY)
31,200
Each
お問い合わせください ›
数量:
100 g
Gibco™ネオマイシンは、ストレプトマイセスフラジエによって生成されます。ポリミキシンB硫酸塩は、細菌リボソームの30Sサブユニットに結合することで作用し、タンパク質の合成および感受性細菌の死亡を阻害します。Gibco™ネオマイシン硫酸塩は、細胞培養における細菌汚染の防止に使用されます。この抗生物質はグラム陰性細菌に対して高い活性を示します。推奨される使用濃度は50 µg/mlです。当社は、細胞培養アプリケーション用のさまざまな抗生物質および抗真菌剤を提供しています。

製品使用
研究目的のみに使用できます。動物やヒトの診断や治療には使用できません。
研究用途にのみご使用ください。診断目的には使用できません。
仕様
培養タイプMammalian Cell Culture, Insect Cell Culture
使用対象(アプリケーション)Bacterial Selection
数量100 g
品質保持期間24 Months
出荷条件Room Temperature
形状Powder
製品タイプAntibiotic
無菌性Non-sterile
Unit SizeEach
組成および保存条件
Storage conditions: 15 to 30°C
Shipping conditions: Ambient
Shelf life: 24 months from date of manufacture

よくあるご質問(FAQ)

Can Neomycin be used in mammalian selection?  Can Neomycin be used instead of Kanamycin in bacterial selection?

No, Neomycin is toxic to mammalian cells. It also causes irreversible damage to kidneys and other organs. Geneticin (aka G418 Sulfate) is a less toxic and very effective alternative for selection in mammalian cells.  Neomycin can be used in bacterial selection, but Kanamycin is the preferred drug to use because of Neomycin's toxicity.

How can I decontaminate my cultures?

When an irreplaceable culture becomes contaminated, researchers may attempt to eliminate or control the contamination.

1. Determine if the contamination is bacteria, fungus, mycoplasma, or yeast. Read more here to view characteristics of each contaminant.
2. Isolate the contaminated culture from other cell lines.
3. Clean incubators and laminar flow hoods with a laboratory disinfectant, and check HEPA filters.
4. Antibiotics and antimycotics at high concentrations can be toxic to some cell lines. Therefore, perform a dose-response test to determine the level at which an antibiotic or antimycotic becomes toxic. This is particularly important when using an antimycotic such as Gibco Fungizone reagent or an antibiotic such as tylosin.

The following is a suggested procedure for determining toxicity levels and decontaminating cultures:

1. Dissociate, count, and dilute the cells in antibiotic-free media. Dilute the cells to the concentration used for regular cell passage.
2. Dispense the cell suspension into a multiwell culture plate or several small flasks. Add the antibiotic of choice to each well in a range of concentrations. For example, we suggest the following concentrations for Gibco Fungizone reagent: 0.25, 0.50, 1.0, 2.0, 4.0, and 8.0 µg/mL.
3. Observe the cells daily for signs of toxicity such as sloughing, appearance of vacuoles, decrease in confluency, and rounding.
4. When the toxic antibiotic level has been determined, culture the cells for two to three passages using the antibiotic at a concentration one- to two-fold lower than the toxic concentration.
5. Culture the cells for one passage in antibiotic-free media.
6. Repeat step 4.
7. Culture the cells in antibiotic-free medium for four to six passages to determine if the contamination has been eliminated.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

What antibiotics do you offer to help control or eliminate cell culture contamination?

Please view the following page to browse the cell culture antibiotics we offer (https://www.thermofisher.com/us/en/home/life-science/cell-culture/mammalian-cell-culture/antibiotics.html).

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

引用および参考文献 (3)

引用および参考文献
Abstract
Hepatitis C virus subgenomic replicons in the human embryonic kidney 293 cell line.
Authors:Ali S, Pellerin C, Lamarre D, Kukolj G,
Journal:J Virol
PubMed ID:14671129
'Hepatitis C virus (HCV) infects liver cells and its replication in other cells is incompletely defined. Human hepatoma Huh-7 cells harboring subgenomic HCV replicons were used in somatic cell fusion experiments with human embryonic kidney 293 cells as a means of examining the permissiveness of 293 cells for HCV subgenomic ... More
DHX9 suppresses RNA processing defects originating from the Alu invasion of the human genome.
Authors:Aktas T, Avsar Ilik I, Maticzka D, Bhardwaj V, Pessoa Rodrigues C, Mittler G, Manke T, Backofen R, Akhtar A
Journal:Nature
PubMed ID:28355180
Transposable elements are viewed as 'selfish genetic elements', yet they contribute to gene regulation and genome evolution in diverse ways. More than half of the human genome consists of transposable elements. Alu elements belong to the short interspersed nuclear element (SINE) family of repetitive elements, and with over 1?million insertions ... More
Structures of the Human PGD
Authors:Wang L, Yao D, Deepak RNVK, Liu H, Xiao Q, Fan H, Gong W, Wei Z, Zhang C
Journal:Mol Cell
PubMed ID:30220562
The signaling of prostaglandin D