Gentamicin (10 mg/mL)
Gentamicin (10 mg/mL)
Gibco™

Gentamicin (10 mg/mL)

ゲンタマイシン硫酸塩は、菌類Micromonospora Purpureaから精製された水溶性抗生物質薬物です。ゲンタマイシンは、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、感受性細菌のタンパク質合成を阻害し、死滅させます。Gibco™ゲンタマイシンは、さまざまなグラム陽性細菌および一部のグラム陰性細菌に対して効果的で、細胞培養の細菌汚染防止のために使用されます詳細を見る
製品番号(カタログ番号)数量
1571007210 x 10 mL
1571006410 mL
製品番号(カタログ番号) 15710072
価格(JPY)
49,200
Each
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数量:
10 x 10 mL
ゲンタマイシン硫酸塩は、菌類Micromonospora Purpureaから精製された水溶性抗生物質薬物です。ゲンタマイシンは、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、感受性細菌のタンパク質合成を阻害し、死滅させます。Gibco™ゲンタマイシンは、さまざまなグラム陽性細菌および一部のグラム陰性細菌に対して効果的で、細胞培養の細菌汚染防止のために使用されます。推奨される使用濃度範囲は0.5~50 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。動物またはヒトの診断もしくは治療には使用できません。

2施設cGMP製造
Gibco™ゲンタマイシンは、ニューヨーク州グランドアイランドにあるcGMP準拠施設で製造されています。この施設は医療機器製造業者としてFDAに登録されており、ISO 13485の認証を受けています。また、サプライチェーン継続性のため、当社のスコットランド施設で製造した同等ののGibco™ゲンタマイシン製品を提供しています(15710-049)。この施設は医療機器製造業者としてFDAに登録されており、ISO 13485の認証を受けています。
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
濃度10 mg/mL
培養タイプMammalian Cell Culture
使用対象(アプリケーション)Prevention of Cell Culture Contamination
数量10 x 10 mL
品質保持期間24 Months
出荷条件Room Temperature
形状Liquid
製品タイプAntibiotic
無菌性Sterile-filtered
Unit SizeEach
組成および保存条件
Storage conditions: 15-30°C
Shipping conditions: Ambient
Shelf life: 24 months from date of manufacture

よくあるご質問(FAQ)

If Gentamicin (10 mg/mL) is accidentally stored at 2-8 degrees C, would it affect the stability of the antibiotic?

No, storing Gentamicin solution for several days at 2-8 degrees C will not have any negative impact on its performance or stability. However, as Gentamicin solution has been shown to be stable at room temperature, the recommended storage temperature is ~25 degrees C.

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

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 (4)

引用および参考文献
Abstract
Comparing Effects of Transforming Growth Factor ß1 on Microglia From Rat and Mouse: Transcriptional Profiles and Potassium Channels.
Authors:Lively S, Lam D, Wong R, Schlichter LC
Journal:Front Cell Neurosci
PubMed ID:29780305
'The cytokine, transforming growth factor ß1 (TGFß1), is up-regulated after central nervous system (CNS) injuries or diseases involving microglial activation, and it has been proposed as a therapeutic agent for treating neuroinflammation. Microglia can produce and respond to TGFß1. While rats and mice are commonly used for studying neuroinflammation, very ... More
Re-Defining Stem Cell-Cardiomyocyte Interactions: Focusing on the Paracrine Effector Approach.
Authors:Mahapatra S, Martin D, Gallicano GI
Journal:J Stem Cells Regen Med
PubMed ID:30018469
'Stem cell research for treating or curing ischemic heart disease has, till date, culminated in three basic approaches: the use of induced pluripotent stem cell (iPSC) technology; reprogramming cardiac fibroblasts; and cardiovascular progenitor cell regeneration. As each approach has been shown to have its advantages and disadvantages, exploiting the advantages ... More
Microglia Responses to Pro-inflammatory Stimuli (LPS, IFN?+TNFa) and Reprogramming by Resolving Cytokines (IL-4, IL-10).
Authors:Lively S, Schlichter LC
Journal:Front Cell Neurosci
PubMed ID:30087595
Microglia respond to CNS injuries and diseases with complex reactions, often called "activation." A pro-inflammatory phenotype (also called classical or M1 activation) lies at one extreme of the reactivity spectrum. There were several motivations for this study. First, bacterial endotoxin (lipopolysaccharide, LPS) is the most commonly used pro-inflammatory stimulus for ... More
Polarized Human Retinal Pigment Epithelium Exhibits Distinct Surface Proteome on Apical and Basal Plasma Membranes.
Authors:Khristov V, Wan Q, Sharma R, Lotfi M, Maminishkis A, Bharti K
Journal:Methods Mol Biol
PubMed ID:29264809
Surface proteins localized on the apical and basal plasma membranes are required for a cell to sense its environment and relay changes in ionic, cytokine, chemokine, and hormone levels to the inside of the cell. In a polarized cell, surface proteins are differentially localized on the apical or the basolateral ... More