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X-VIVOTM 20 Serum-free Hematopoietic Cell Medium

X-VIVOTM 20 Serum-free Hematopoietic Cell Medium

Catalog #: 04-448Q

X-VIVOTM 20, with L-Glutamine, gentamicin and phenol red, xenofree,1 L

 

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Product Overview

X-VIVOTM 20 Medium is optimized to support the generation of lymphokine activated killer (LAK) cells from monocytedepleted peripheral blood lymphocytes (PBL) at high density. Initial cell densities between 2.0 – 3.0 × 107 cells/ ml can be used to successfully generate LAK cells. X-VIVOTM 20 Medium may also be used as a growth medium for PBL and tumor infiltrating lymphocytes (TIL).

All BioWhittakerTM Cell Culture Media products are for Research Use Only (RUO) and are not approved for human or veterinary use or for use in clinical or in vitro diagnostic procedures. If you require GMP grade media, contact Lonza for more details.

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Applications

– Proliferation of peripheral blood lymphocytes

– Proliferation of tumor infiltrating lymphocytes

– Cryopreservation of human tissue

– Cultivation of human monocytes and macrophages

– Cultivation of stem cells – Cultivation of dendritic cells

Storage and Content

1L bottle
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SDS, CoA, and Instructions

Certificate of Analysis (CoA)

Please enter Lot Number, including all zeros, located on the product label and please take into account that it is case sensitive.

  • References - X-Vivo™

    Overview of relevant references
  • TechSheet - X-VIVO™ Media Systems

    Instructions for how to use the X-VIVO™ Media Series
  • Human CD34+ Cells Technical information and instructions for use

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Educational Material

Brochures, White Papers etc.

  • Developing Patient-specific Cell Therapy Manufacturing Processes

    Poster presentation about patient-specific cellular therapies and their tremendous potential for being able to treat life threatening diseases where there are currently no cures.
  • CAR T cells in Cancer Therapy

    A poster developed by Nature Reviews in conjunction with Lonza to present CAR T cells in cancer therapy. This poster demonstrates the recognition of tumor peptides by T cells, CAR T cell manufacturing, the types of chimeric antigen receptors and a timeline of CAR development over more than 30 years.
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