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PMEF-HL

EmbryoMax® Primary Mouse Embryonic Fibroblasts

Mouse

Sinónimos:

Hygro MEF Feeder Cells, Hygro Mouse Feeder Cells, Hygro-MEFs, Hygromycin Restistant PMEFs, MEF Feeder Cells, hygro PMEFs, hygro MEFs, MEFs, Mouse Feeder Cells

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Talla/SKUDisponibilidadPrecio
5 vials
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458,00 €

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UNSPSC Code:
41106509
NACRES:
NA.75
eCl@ss:
32011203
Biological source:
mouse
Manufacturer/tradename:
Specialty Media, EmbryoMax®

458,00 €


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Nombre del producto

EmbryoMax® Primary Mouse Embryonic Fibroblasts, PMEF, Hygro Resistant, Strain C57/BL6, Not Treated, Passage 3

biological source

mouse

Quality Segment

manufacturer/tradename

Specialty Media, EmbryoMax®

technique(s)

cell culture | stem cell: suitable

input

sample type: mouse embryonic stem cell(s)
sample type primary embryotic fibroblasts (PMEFs)
sample type induced pluripotent stem cell(s)

shipped in

liquid nitrogen

storage temp.

-140 to -196°C

General description

Primary Mouse Embryo Fibroblasts, hygromycin resistant, strain C57/BL6, are not Mytomycin C treated and serve as a feeder layer for both mouse and human ES/IPS cells. MEF cells are resistant to hygromycin. The cells are provided at passage 3 and can be further expanded before freezing for later use.

Plating MEF Feeder Cells

Procedure:

1. Prior to thawing PMEF feeder cells, coat plates/flasks with Gelatin solution.
2. Thaw PMEF vial(s) quickly in a 37 °C water bath and transfer to a 15 mL tube (already containing 10 mL of warm PMEF Feeder Cell Medium). Gently invert the tube to distribute, and centrifuge at 300 xg for 4–5 minutes.
3. Remove supernatant and resuspend the cell pellet in warm PMEF Feeder Cell Medium.
4. Remove the Gelatin solution from plates/flasks, and aliquot the PMEF feeder cell suspension at the densities recommended in Table 4.1 of the mouse ES protocol guide
5. Incubate the PMEF Feeder cells at 37 °C with 5% CO2. Use Figures 4A, B and C in the mouse ES protocol guide as a guide for an estimate of correct PMEF density and
appearance. Gelatinized plates may be used for 12–14 days.
The EmbryoMax range of PMEF cells provides researchers with a convenient solution for ES cell culture by eliminating the need for time consuming feeder cell isolation and preparation. Many embryonic stem cell culture protocols necessitate the use of primary mouse embryo fibroblast (PMEF) cells. In these protocols, ES cells are typically cultured on a monolayer of PMEF feeder cells. Feeder cells perform two important roles in stem cell culture: they secrete several important growth factors into the medium, which help maintain pluripotency, and they provide a cellular matrix for ES cells to grow.

Biochem/physiol Actions

Primary Mouse Embryo Fibroblasts

Packaging

5-6x106 ea

Physical form

The cells are provided frozen into individual vials, containing approximately 5-6 x 106 fibroblasts per vial, and are sold as a pack of 5 vials and supplied at passage 3.

Preparation Note

After receipt, vials should be stored at -80°C. If storing for longer than 6 months, store in the vapor phase of liquid nitrogen (make sure the cap is tight) for up to 2 years.

Legal Information

EmbryoMax is a registered trademark of Merck KGaA, Darmstadt, Germany


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Clase de almacenamiento

12 - Non Combustible Liquids

flash_point_f

does not flash

flash_point_c

does not flash


Listados normativos

Los listados normativos se proporcionan para los productos químicos principalmente. Para los productos no químicos sólo se puede proporcionar información limitada. Si no hay ninguna entrada, significa que ninguno de los componentes está en la lista. Es obligación del usuario garantizar el uso seguro y legal del producto.

10043-52-4

CAS No.


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Preguntas

  1. Would it be possible to get a more precise information on the dissection of these fibroblasts -- i.e. were the head, vertebral column, dorsal root ganglia, and visceral organs removed? Or were these fibroblasts obtained from limbs only?

    1 respuesta
    1. The dissection requirement is that the head, liver, and visceral tissues be taken. Unfortunately, other than the source of the dissected tissues, the specific origin is not reported.

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