Sulfato de neomicina
Sulfato de neomicina
Gibco™

Sulfato de neomicina

La neomicina Gibco™ se produce por Streptomyces fradiae. El sulfuro de Polimixina B actúa mediante la creación de una uniónMás información
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Número de catálogoCantidad
21810031100 g
Número de catálogo 21810031
Precio (MXN)
-
Cantidad:
100 g
La neomicina Gibco™ se produce por Streptomyces fradiae. El sulfuro de Polimixina B actúa mediante la creación de una unión a la subunidad 30S del ribosoma bacteriano, lo que conduce a la inhibición de la síntesis de proteínas y la muerte de bacterias susceptibles. El sulfato de neomicina Gibco™ se utiliza para la prevención de la contaminación bacteriana de cultivos celulares. Este antibiótico es altamente activo contra bacterias gramnegativas. La concentración de trabajo recomendada es de 50 µg/ml. Ofrecemos una gran variedad de antibióticos y antimicóticos para aplicaciones de cultivos celulares.

Uso del producto
Para uso exclusivo en investigación: No se ha diseñado para uso diagnóstico o terapéutico en animales o humanos.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Tipo de cultivoCultivo celular de mamíferos, cultivo celular de insectos
Para utilizar con (aplicación)Selección bacteriana
Cantidad100 g
Duración de almacenamiento24 meses
Condiciones de envíoTemperatura ambiente
FormularioPolvo
Tipo de productoNeomicina
EsterilidadNo estéril
Unit SizeEach
Contenido y almacenamiento
Condiciones de almacenamiento: De 15 a 30 °C
Condiciones de envío: Ambiente
Vida útil: 24 meses a partir de la fecha de fabricación

Preguntas frecuentes

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.

Citations & References (3)

Citations & References
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