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Merck

12007C

Suero fetal bovino

Australia origin, γ-irradiated, sterile-filtered, suitable for cell culture

Sinónimos:

FBS, FCS, Suero, sueros

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UNSPSC Code:
12352207
NACRES:
NA.71
MDL number:
Biological source:
bovine fetus
Origin:
Australia origin
Sterility:
γ-irradiated, sterile-filtered
Shipped in:
dry ice
Servicio técnico
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biological source

bovine fetus

Quality Level

sterility

γ-irradiated, sterile-filtered

product line

FBS Premier

composition

Hemoglobin, ≤25 mg/dL

origin

Australia origin

technique(s)

cell culture | mammalian: suitable

impurities

≤10 EU/mL endotoxin

shipped in

dry ice

storage temp.

−20°C

Application

El FBS procedente de Australia se utiliza en una amplia variedad de aplicaciones de cultivo celular. El FBS proporciona muchos factores no definidos de promoción del crecimiento y de mejora de la supervivencia de las células en cultivo. Australia tiene la mejor clasificación posible en relación con el riesgo geográfico de encefalopatía espongiforme bovina (BSE) según indicación del Comité Científico Directivo sobre el riesgo geográfico de la encefalopatía espongiforme bovina. La clasificación para Australia es nivel GBR I.

Preparation Note

Irradiación gamma mediante el proceso SER-TAIN (25-35kGy).

Analysis Note

  • Analizada la presencia de endotoxinas y hemoglobina
  • Se ha estudiado la presencia de bacterias, virus y micoplasmas
  • Filtrado triple con membrana de 0,1 micra bajo condiciones asépticas

Other Notes

(Referencia anterior del producto F3297)

Legal Information

SER-TAIN is a trademark of Sigma-Aldrich Co. LLC


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Clase de almacenamiento

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Contenido relacionado

SAFC Biosciences - The accomplished serum provider. In today's increasingly regulated world it is essential to have complete confidence in the origin of your serum. Australian-origin Fetal Bovine Serum (FBS) is recognized as the safest serum available in commercially viable volumes.

SAFC Biosciences has established process parameters and controls for maximum inactivation of microbial contaminants while maintaining product integrity through its validation of the gamma irradiation process for serum products. The validation study evaluated package configurations, process temperatures, radiation dose response and radiation distribution within the packages. The study was conducted at both pilot scale (100 mL samples) and production scale (500 mL, 1000 mL, 3 L and 4 L samples).

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