Gentamicin/Amphotericin Solution
Gentamicin/Amphotericin Solution
Gibco™

Gentamicin/Amphotericin Solution

Gentamicin 및 amphotericin B에 대한 무균 농축(500×) 항생항진균 용액(10 × 1 ml vials⁄pkg). Gentamicin⁄Amphotericin Solution 10-Pak 하나는 500 ml 기본자세히 알아보기
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카탈로그 번호수량
R0151010 x 1 mL
카탈로그 번호 R01510
제품 가격(KRW)
148,000
Online offer
Ends: 31-Dec-2025
155,000
할인액 7,000 (5%)
Each
카트에 추가하기
수량:
10 x 1 mL
제품 가격(KRW)
148,000
Online offer
Ends: 31-Dec-2025
155,000
할인액 7,000 (5%)
Each
카트에 추가하기
Gentamicin 및 amphotericin B에 대한 무균 농축(500×) 항생항진균 용액(10 × 1 ml vials⁄pkg). Gentamicin⁄Amphotericin Solution 10-Pak 하나는 500 ml 기본 배지 10개를 보충하기 충분합니다. 동물 유래성분 무함유.
For Research Use Only. Not for use in diagnostic procedures.
사양
농도500 X, 125 μg/mL Amphotericin B, 5 mg/mL Gentamicin
제품라인Cascade Biologics
권장 스토리지

minus 20 degrees C

배송 조건Dry Ice
멸균 필터링됨Yes
검증된 애플리케이션Prevention of Cell Culture Contamination
물리적 형태Liquid
수량10 x 1 mL
유형Amphotericin B, Gentamicin
Unit SizeEach

자주 묻는 질문(FAQ)

What alternative product do you offer for Gentamicin/Amphotericin Solution (Cat. No. R01510)?

We recommend ordering Gentamicin (10 mg/mL) (Cat. No. 15710064, 15710072) and Amphotericin B (250 µg/mL) (Cat. No. 15290026, 156290018) and mixing them together 1:1 to get a similar product as Gentamicin/Amphotericin Solution (Cat. No. R01510).

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.

인용 및 참조 문헌 (7)

인용 및 참조 문헌
Abstract
Decellularized skeletal muscles display neurotrophic effects in three-dimensional organotypic cultures.
Authors:Raffa P, Scattolini V, Gerli MFM, Perin S, Cui M, De Coppi P, Elvassore N, Caccin P, Luni C, Urciuolo A
Journal:Stem Cells Transl Med
PubMed ID:32578968
'Skeletal muscle decellularization allows the generation of natural scaffolds that retain the extracellular matrix (ECM) mechanical integrity, biological activity, and three-dimensional (3D) architecture of the native tissue. Recent reports showed that in vivo implantation of decellularized muscles supports muscle regeneration in volumetric muscle loss models, including nervous system and neuromuscular ... More
In Vitro Model of the Epidermis: Connecting Protein Function to 3D Structure.
Authors:Arnette C, Koetsier JL, Hoover P, Getsios S, Green KJ
Journal:Methods Enzymol
PubMed ID:26778564
'Much of our understanding of the biological processes that underlie cellular functions in humans, such as cell-cell communication, intracellular signaling, and transcriptional and posttranscriptional control of gene expression, has been acquired from studying cells in a two-dimensional (2D) tissue culture environment. However, it has become increasingly evident that the 2D ... More
Low-level arsenic causes proteotoxic stress and not oxidative stress.
Authors:Dodson M, de la Vega MR, Harder B, Castro-Portuguez R, Rodrigues SD, Wong PK, Chapman E, Zhang DD
Journal:Toxicol Appl Pharmacol
PubMed ID:29408041
'Prolonged exposure to arsenic has been shown to increase the risk of developing a number of diseases, including cancer and type II diabetes. Arsenic is present throughout the environment in its inorganic forms, and the level of exposure varies greatly by geographical location. The current recommended maximum level of arsenic ... More
Erratum: Long-range self-organization of cytoskeletal myosin II filament stacks.
Authors:Hu S, Dasbiswas K, Guo Z, Tee YH, Thiagarajan V, Hersen P, Chew TL, Safran SA, Zaidel-Bar R, Bershadsky AD
Journal:Nat Cell Biol
PubMed ID:28248306
Cholesterol crystals increase vascular permeability by inactivating SHP2 and disrupting adherens junctions.
Authors:Mani AM, Chattopadhyay R, Singh NK, Rao GN
Journal:Free Radic Biol Med
PubMed ID:29782988
To understand the adverse effects of cholesterol crystals on vascular homeostasis, we have studied their effects on endothelial barrier function. Cholesterol crystals increased endothelial barrier permeability in a dose and time dependent manner. In addition, cholesterol crystals induced tyrosine phosphorylation of VE-cadherin and a-catenin, disrupting endothelial AJ and its barrier ... More