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Technical library

Our technical library provides in-depth scientific and product-specific information and expert guidance to support your research. For more general topics and quick answers, please refer to the FAQs.

Items 151-160 of 283

  • The Certificates of Analysis can easily be downloaded from our CoA search page. Simply type in the lot number indicated on the cryovial/TC-flask and click the SEARCH button.

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  • You need to have experience working under sterile conditions and under a laminar flow hood. It is of advantage to have experience with other cell types and/or cell lines. If you are a beginner in cell culture and would like to establish a cell culture lab, we will assist you in working with PromoCell Normal Human Cells.

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  • Serum turbidity is usually caused by cryoprecipitation of lipid components during freezing and thawing. The more times the serum is subjected to freeze/thaw cycles, the more turbidity is noticed.

    It can be minimized by freezing the serum in aliquots at -20°C and thawing these aliquots individually at the time of use.

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  • Differentiation of hMSC into mature adipocytes takes approx. 2 weeks. You can keep the adipocytes for up to 3 weeks in the MSC Adipogenic Differentiation Medium. After 3 weeks we recommend to switch to PromoCell's Adipocyte Nutrition Medium (C-27438).

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  • Changing the medium every 2-3 days, the neuronally differentiated MSC can be kept in culture for up to 2 weeks.

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  • Human Mesenchymal Stem Cells have retained the ability to differentiate into a variety of cell types including fat cells, chondrocytes, and osteoblasts. PromoCell supply hMSC from 3 different tissues: bone marrow (hMSC-BM; C-12974), umbilical cord matrix (hMSC-UC; C-12971), and adipose tissue (hMSC-AT; C-12977).

    • MSC-BM show very good differentiation into bone cells but also into chondrocytes and fat cells when the respective Differentiation Media is used.
    • MSC-UC have a high potential to differentiate into chondrocytes but only weak potential for fat or bone cell differentiation.
    • In contrast, MSC-AT differentiate very well into fat and bone cells but only moderately into chondrocytes.

    In other words, to obtain a high percentage of bone cells, MSC-BM or MSC-AT are the cells of choice. There are of course lot-to-lot variations and the differentiation will decrease from passage to passage. If you need MSCs with a particularly high osteoblast differentiation capacity, you can contact our Scientific Support before placing your order so that we can select an appropriate cell lot for you.

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  • The population doubling times for PromoCell hMSC (hMSC-BM, hMSC-AT, hMSC-UC) are typically ≤ 30 hrs when using Mesenchymal Stem Cell Growth Medium 2 (C-28009). If you seed the hMSC at 4.000 cells/cm2, it will take between 4-7 days until they reach subconfluency.

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  • Our MNC lots are checked for the rate of lymphocytes, monocytes and granulocytes w/o staining by FSC/SSC using a flow cytometer. A sample plot is attached. For our purified CD14+ monocytes we additionally perform a CD14+ staining.

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  • It takes 7-8 days to generate fully mature myeloid dendritic cells.

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  • According to our experience, they can be maintained for 3 to a maximum of 7 days. However, the morphology will change and they will look more and more "degenerate".

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