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  • ¥500 - 5000
  • polyplus
  • 美国
  • 101000046
  • 2025年07月10日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 保存条件

      2~8℃

    • 保质期

      1年

    • 英文名

      jetPRIME® transfection reagent

    • 库存

      50

    • 供应商

      北京百奥创新科技有限公司

    • 规格

      1.5 mL

    jetPRIME® 通用型DNA/siRNA转染试剂(101000046)

    Polyplus全国代理——北京百奥创新科技有限公司!

    产品特性:

    ReagentjetPRIME®
    Molecule deliveredDNA, siRNA, DNA & siRNA

     

     

    Applications

    Plasmid transfection
    Genome editing
    Virus production
    siRNA transfection
    Co-delivery of different nucleic acids
    Cell typesAdherent cell lines grown in presence of serum

     

    Number of transfections

    1.5 ml of jetPRIME® transfection reagent is sufficient

    to perform up to 1500 transfections in 24-well plates or 375 transfections in 6-well plates

    StorageStore jetPRIME® at 5 °C ± 3°C
    Provided withjetPRIME® buffer

    产品概况:

    jetPRIME® is a powerful and versatile DNA and siRNA transfection reagent for day-to-day experiments that leads to efficient and reliable scientific results. jetPRIME® ensures high DNA transfection efficiency and excellent gene silencing in a variety of adherent cells. jetPRIME® is also ideal for DNA/siRNA co-transfection or co-delivery of several plasmids. Furthermore, our jetPRIME® reagent is very gentle on cells since it requires low amounts of reagent and nucleic acid during transfection.

    产品描述:

    Superior transfection efficiency

    jetPRIME® is a powerful transfection reagent for day-to-day experiments. It leads to unusually high percentage of transfected adherent cell lines of various origins as well as primary cells.

    Superior transfection efficiencies ranging between 70 and 90% were obtained with jetPRIME® reagent versus the top competitor’s reagent for several commonly used cell lines (Fig.1 & Fig.2).

    产品细节图片1

    Fig. 1: Comparative transfection efficiency of jetPRIME versus its main competitor. Transfection efficiency was assessed by FACS analysis in various cell lines 24 h after transfection in 24-well plates. Conditions were used according to the manufacturer’s recommendation for both Lipofectamine® 2000 and for jetPRIME®.

    产品细节图片2

    Fig. 2: Comparative transfection efficiency of jetPRIME® versus Lipofectamine® 3000. Transfection efficiency was assessed by FACS analysis in various cell lines 24 h after transfection in 96-well plates or 24-well plates. Conditions were used according to the manufacturer’s recommendation for lipofectamine® 3000 and for jetPRIME®.

    Cost-effective: less DNA and less reagent

    jetPRIME® is apowerful in vitro transfection reagent that requires a small amount of reagent and plasmid DNA, making its use very cost-effective (Table 1).

    产品细节图片3

    Table 1: Recommended conditions to use. Amounts of DNA and reagent (jetPRIME® and competitors) per well in 6-well plate for transfection according to manufacturers’ recommendations.

    In addition to reducing costs, using less DNA also minimizes adverse cytotoxic effects triggered by transfection. Hence, jetPRIME® is the reagent of choice for high transfection efficiency with excellent cell viability.

    Better cell viability

    jetPRIME® is extremely gentle on cells during transfection leading to increased cell viability and improved transfection results. Cells transfected with jetPRIME® are healthy, while major cytotoxicity is observed with competitors (Fig.3).

    产品细节图片4

    Fig. 3: Cell viability 24h after transfection. Phase contrast microscopy of HeLa cells 24 h after transfections performed according to the manufacturer’s recommendations for each reagent.

    Easy to use protocol

    jetPRIME® is an easy-to-use transfection reagent (Fig.4):

    • Fast and easy to scale up and down

    • Compatible with serum and antibiotics

      产品细节图片5

    Fig. 4: jetPRIME® protocol. Convenient protocol for DNA, siRNA and co-transfection of DNA and siRNA.

    产品应用:

    Plasmid transfection

    jetPRIME® leads to remarkably high percentages of transfected adherent cell lines of various origin, as well as primary cells (Table 1).

    产品细节图片6

    Table 1: Transfection efficiency of various cell types using jetPRIME®. The percentage of GFP-positive cells was determined by FACS analysis 24 h after transfection.

    Plasmids are small circular DNA molecules that are commonly found in bacteria. Plasmids exist and replicate separately from chromosomal DNA and in bacteria they often carry genes that are beneficial for bacterial survival. Plasmids can be deliberately introduced into desired cells and utilized to overexpress a gene of interest in a specific cell line. This procedure is called DNA transfection and is a commonly used method for studying gene function or protein of interest.

    Genome editing

    The use of the CRISPR/Cas9 system in mammalian cells has recently emerged as a very convenient way to modify the cell genome at a specific locus. It involves transient transfection into mammalian cells of either (a) one or several plasmids coding for Cas9, the specific gRNA and eventually the sequence to be inserted, or (b) a mix of one or two plasmids and an RNA molecule (the gRNA).

    siRNA transfection

    jetPRIME® leads to over 90% knockdown of endogenous gene expression in a variety of cell lines. For example, jetPRIME®-mediated transfection of HeLa cells with 10 nM siRNA duplexes targeting endogenous lamin A/C in HeLa cells drastically reduces lamin A/C gene expression to barely detectable level (Fig. 1).

    产品细节图片7

    Fig. 1: Endogenous lamin A/C silencing using jetPRIME®HeLa cells were transfected with 10 nM of 21-mer lamin A/C siRNA. After 48 h, lamin A/C silencing was assessed by immunofluorescence microscopy using an antibody against lamin A/C .

    Co-transfection of different nucleic acids

    jetPRIME® is well suited for DNA and siRNA/ miRNA co-transfection experiments or co-delivery of several DNA plasmids.

    We performed DNA and siRNA delivery with jetPRIME® and observed highly efficient gene silencing in a variety of cell lines with very low toxicity. Over 90% silencing is achieved in adherent cells, using 10 nM siRNA (Fig. 2).

    产品细节图片8

    Fig. 2: Exogenous luciferase silencing in several cell lines after DNA & siRNA cotransfection using jetPRIME®. Experiments were performed with 400 ng p4CMV-Luc and 10 nM of luciferase siRNA per well in 6-well plates.

    产品优势:

    • High DNA transfection efficiency

    • Low amounts of nucleic acid

    • Superior cell viability

    • ONE reagent for DNA and/or siRNA transfections

    • Cost-effective

    订购信息:

    Reference NumberAmount of reagentAmount of buffer
    101000027jetPRIME® 0.1 mL5 ml
    101000015jetPRIME® 0.75 mL60 ml
    101000046jetPRIME® 1.5 mL2 x 60 ml
    101000001jetPRIME® 5 x 1.5 mL10 x 60 ml
    201000003xjetPRIME® buffer 60 ml

    Polyplus全国代理——北京百奥创新科技有限公司!

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