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SignaGen转染试剂 for CHO Cells

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  • ¥1560
  • SignaGen
  • 美国
  • Catalog #: SL100489-CHO
  • 2026年01月07日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保质期

      一年

    • 英文名

      GenJet™ In Vitro DNA Tranfection Reagent for CHO Cells

    • 库存

      现货 大量

    • 供应商

      济南美中清水湾生物科技有限公司

    • 保存条件

      4°C

    Description
    GenJet™ DNA In Vitro Tranfection Reagent for CHO is pre-optimized for transfecting Chinese Hamster Ovary (CHO) cells. Refer to the following optimal transfection conditions for maximal transfection efficiency on CHO cells. GenJet™ reagent, 1.0 ml, is sufficient for 300 to 600 transfections in 24 well plates or 50 to 100 transfections in 6 well plates.
    Summary of Optimal Transfection Conditions:
    Confluence on the day of transfection
    Cell culture conditions
    GenJet™ (µl) : DNA (µg) Ratio
    Diluent for DNA and Transfection Reagent
    Incubation Time to Form GenJet™/DNA Complex
    Presence of Serum/Antibiotics during Transfection
    Change Medium After Transfection
    Maximal Efficiency

    Transfection Results:
    Reporter Gene
    Plasmid
    Efficiency (GFP %)

    ~90%
    DMEM with 4.5 g/L glucose, 10% FBS
    3:1
    Serum-free DMEM with 4.5 g/L glucose
    15 minutes at RT
    Yes
    Yes, 16~24 Hours After Transfection
    48 hours


    EGFP
    pEGFP-N3 (CMV promoter)
    90%
    Storage Condition
    Store at 4 °C. If stored properly, the product is stable for 12 months or longer

    产品细节图片1
    A Picture Showing Transfection Efficiency of GenJet™ Reagent on CHO Cells. CHO cells were grown per ATCC recommended culture medium and transfected with pEGFP-N3 by GenJet™. The efficiency was checked 24 hours post transfection

    Data Sheet 产品细节图片2


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    图标文献和实验
    相关实验
    • Establishment of Stable Transfectant of CHO Lec Cells

        Purpose and Backgrounds CHO lec 3.2.8.1 cells CHO Lec 3.2.8.1 cells have four independent mutations in the N- and O- glycosylation pathways (Stanley, 1989). N-linked carbohydrates produced by CHO Lec 3.2.8.1 cells are all of the high

    • Harvesting GPI-Anchored Proteins From CHO Cells

      Glycosyl-phosphatidylinositol (GPI)-anchored proteins bound to the outer surface of cell membranes (1 ,2 ) can be selectively released in a soluble form by the action of a highly specific bacterial enzyme, phosphatidylinositol-phospholipase

    • Stable Expression of Chimeric Heavy Chain Antibodies in CHO Cells

      Camelid single domain antibodies fused to noncamelid Fc regions, also called chimeric heavy chain antibodies (cHCAb), offer great potential as therapeutic and diagnostic candidates due to their relatively small size (80 kDa) and intact Fc

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