PAN-Biotech Panserin 293A: Serum-free medium for HEK293 cells in adherent culture, w: L-Glutamine, 500 ml cell culture medium
PAN-Biotech Panserin 293A: Serum-free medium for HEK293 cells in adherent culture, w: L-Glutamine, 100 ml cell culture medium
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Panserin 293A: Serum-free medium for HEK293 cells in adherent culture, w: L-Glutamine

P04-710608M
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$125.00
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$125.00
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Introduction

PAN-Biotech Panserin 293A is a ready-to-use medium for the serum-free cultivation of HEK293 cells (Human Embryonic Kidney) in adherent culture. Serum-containing medium can be replaced directly.

Panserin 293A promotes the attachment of the cells and high cell growth rates, and has been used for the expression of recombinant proteins and the proliferation of AVVs and LVVs. The efficient serum-free cultivation can be supported by higher seeding densities.

    Cell Type: HEK cells
    Culture Type: Adherent Culture
    Liquid / Powder: liquid
    Product Category: Serum-Free Media
    Glutamine With L-Glutamine
    Size: Various
    Sterile: Yes
    Storage Temperature: +2°C - +8°C

    Composition

    Based on DMEM, Panserin 293A contains additional trace elements, proteins, cholesterol, lipids, vitamins and hormones. The total content of proteins and animal-derived components is lower than 0.2% w/v.

    Application

    Panserin 293A is a particularly enriched medium optimized for the growth of HEK293 cells in adherent culture. HEK293 is frequently used for the expression of recombinant proteins and the proliferation of adenoviruses. Panserin 293A promotes a rapid attachment of the cells and high cell growth rates.

      Storage conditions & stability

      Store at +2°C - +8°C.

      Documents

      Product References

      • Burton, Bronwen R et al. “Variant proteins stimulate more IgM+ GC B-cells revealing a mechanism of cross-reactive recognition by antibody memory.” eLife vol. 7 e26832. 1 May. 2018, doi:10.7554/eLife.26832
      • Hanauer, Jan Rh et al. “Enhanced lysis by bispecific oncolytic measles viruses simultaneously using HER2/neu or EpCAM as target receptors.” Molecular therapy oncolytics vol. 3 16003. 24 Feb. 2016, doi:10.1038/mto.2016.3

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