SKU: G001  / 
    CAS Number: 108321-42-2

    G418 Disulfate

    1,082,380.00Rp - 30,000,750.00Rp
    G418 Disulfate

    G418 Disulfate (syn: Geneticin) is an aminoglycoside antibiotic isolated from Micromonospora rhodorangea and is similar in structure to Gentamicin B1.  G418 is an analog of Neomycin Sulfate and has a similar mechanism to Neomycin.  It has a broad range of in vitro and in vivo antibacterial activity.  It is routinely used for gene selection in cell culture, for selection and maintenance of both prokaryotic and eukaryotic cells transfected with the neomycin resistance gene (neo). 

    G418 Disulfate is soluble in water.

    We also offer:
    • G418 Disulfate, EvoPure® (G030)
    • G418 Disulfate (Low Endotoxin) (G048)
    • G418 Disulfate ReadyMadeTM Solution (G020)
    Mechanism of Action G418 Disulfate and other aminoglycosides prevent protein synthesis at the early stages of elongation, post-initiation, initiation of translation.  Resistance to G418 Disulfate is conferred by the Neomycin resistance gene (neo) from either Tn5 or Tn601 (903) transposons. Cells transfected with resistance plasmids containing the neo gene can express aminoglycoside 3'-phosphotransferase (APT 3' I or APT 3' II) which covalently modifies G418 to 3-phosphoric G418,  which has negligible potency and has low-affinity for prokaryotic and eukaryotic ribosomes.
    Spectrum G418 Disulfate is toxic to susceptible bacteria, fungi, yeast, protozoa, helminths, mammalian cells, and plants.
    Microbiology Applications G418 Disulfate is used as a gene selection agent during transfection of eukaryotic cells.
    Eukaryotic Cell Culture Applications

    G418 Disulfate is routinely used as a selection agent in cell culture after transfection of eukaryotic cells.   Resistant cells express the neo gene which produces aminoglycoside 3'-phosphotransferase (APT 3' I or APT 3' II),  a protein that confers resistance to G418 Disulfate and other aminoglycoside antibiotics.

    Optimal working concentrations:

      • Mammalian cell lines:  200 mg/L – 1000 mg/L
      • Bacteria and algae:  ≤5 mg/L

    The optimal working concentration of G418 Disulfate to select for resistant clones depends on the cell line, reagent quality, reagent lot, media, growth conditions, cell density, cell metabolic rate, cell cycle phase, and plasmid quality.  A kill curve should  be performed to determine the optimal concentration for each experimental system.

    Use the following guide to determine the appropriate concentration:

      • 5 mg/L - 1400 mg/L (mammalian cells)
      • 0.1 mg/L - 50 mg/L (bacteria and algae)

    A working concentration of 200 mg/L is usually sufficient after resistant mammalian clones are selected and can be used for maintenance until stable resistant clones are selected.

    Genetically engineered embryonic stem cells were transfected with a fusion gene containing the alpha-cardiac myosin heavy chain (MHC) promoter driving the aminoglycoside phosphotransferase (neo gene).  Selection protocols used G418 +/-retinoic acid.  Enrichment of cardiomyocytes could be achieved in cultures treated with G418 alone or with retinoic acid (Zandstra et al, 2003).

    Human induced pluripotent stem cells (hiPSCs) can be used to study skeletal muscle differentiation in vitro and the expression of transcription factors, with focus on MYOD1. One of the tools, piggyBac transposon vector, is transduced into hPSCs and cells are selected with G418 or Puromycin and screened for the appropriate MYOD1-hPSC clones showing highly efficient skeletal muscle differentiation.  Multiple MYOD1-hPSC clones should be analyzed.  The selection marker plays an important role in increasing transgene expression efficiency.  Authors found Puromycin selection resulted in high-level transgene expression and efficient skeletal muscle differentiation even in bulk culture of MYOD1-hiPSCs.  This bulk differentiation system may help generate disease models for analyzing pathophysiological mechanisms of muscular disorders (Rashid et al, 2023). 

    The Selectivity Factor is a quantifiable measure of how efficient an antibiotic is during the process of gene selection.  Our R&D team tested the selectivity factor of G418 Disulfate for BHK-21 and HeLa cell lines.  They found that G418 is an ideal selection antibiotic for transfected BHK-21 cells but not optimal for HeLa cells.  The method uses a modified MTT assay, which can be used to numerically determine the antibiotic efficiency (Delrue et al, 2018).  For more information about the Selectivity Factor, click here.

    For more information on relevant cell lines, culture medium, and working concentrations, please visit the Cell-Culture Database.
    Molecular Formula C20H40N4O10 · 2H2SO4
    Biological Assay ED50 Resistant: ≥2500 µg/mL
    ED50 Sensitive: ≤400 µg/mL
    Elemental Analysis

    Carbon: 28.80-36.07%
    Hydrogen: 5.76-7.76%
    Nitrogen: 6.72-8.41%
    Water of Hydration: 0-6

    Ammonia: ≤1.0%
    Documents G418_Disulfate_Kill_Curve_Protocol.pdf|Plasmid_DNA_Transfection_Protocol.pdf|Selection_of_Stable_Transfected_Cell_Lines_Protocol.pdf
    References

    Aragão FJL and Brasileiro ACM (2002)  Positive, negative and marker-free strategies for transgenic plant selection. Braz. J. Plant Physiol. 14(1):1-10

    Davis BD (1987)  Mechanism of bactericidal action of aminoglycosides.  Microbiol. Rev. 51(3):341-350  PMID 3312985

    Delrue I, Pan Q, Baczmanska AK, Callens BW and Verdoodt LLM (2018)   Determination of the selection capacity of antibiotics for gene selection.  Biotechnol. J. 13(8):1700747  PMID 29436782

    Lin-Cereghino, J et al (2008)  Direct selection of Pichia pastoris expression strains using new G418 resistance vectors.  Yeast 25:293-299  PMID 18327886

    Rashid M et al (2023)  Simple and efficient differentiation of human iPSCs into contractible skeletal muscles for muscular disease modeling.  Sci. Rep. 13:8146

    Shin Y (2007)  Selection of NptII transgenic sweet potato plants using G418 and paromomycin.  J. Plant Biol. 50(2):206-212

    Zandstra PW et al (2003)  Scalable production of embryonic stem cell-derived cardiomyocytes.  Tissue Eng. 9(4):767-778  PMID 13678453
    Protocols
    G418 Disulfate Kill Curve Protocol

    Background:
    G418 Disulfate (Syn: Geneticin; G418 Sulfate) is routinely used to select for successfully transfected mammalian cells that express the neo antibiotic resistance gene in addition to the gene of interest. The neo gene encodes amino-glycoside 3’-phosphotransferase; an enzyme which confers resistance to G418 disulfate and neomycin. Before stable transfected cell lines can be selected, the optimal G418 disulfate concentration needs to be determined by performing a kill curve titration. The optimal concentration of G418 Disulfate suitable for selection of resistant mammalian clones is dependent on the cell lines, media, growth conditions, and the quality of G418 Disulfate. Due to minor batch-to-batch variability, it is necessary to perform a kill curve for every new cell type and new batch of G418 Dsulfate.
     
    Preparation and storage of G418 Disulfate solution:
    • Prepare stock solution by dissolving G418 Disulfate in water at a concentration of 50 mg/ml.
    • Sterile filter the solution using 0.45 µm filter.
    • Store solution at 2-8°C after use.
    Kill curve/G418 Titration Protocol:
    1. Seed cells of the parental cell line in a 24-well plate at different densities (50,000 – 100,000 and 200,000 cells/ml) and incubate the cells for 24 hours at 37°C.
    2. Remove medium and then add medium with varying concentrations of antibiotic (0, 50, 100, 200, 400, 600, 800, and 1,000 μg/ml) and incubate at 37°C.
    3. Refresh the selective medium every 3-4 days and observe the percentage of surviving cells over time (e.g. by EMA vs Hoechst staining, flow cytometry or MTT assay).
    4. Determine the lowest concentration of antibiotic that kills a large majority of the cells within 14 days. This concentration should be used for selection of a stable transfected cell line.
    5. If necessary, repeat the experiment to narrow the antibiotic concentration range.


    Plasmid DNA Transfection Protocol

    Background:
    Once the appropriate antibiotic concentration to use for selection of the stable transfected cells has been determined by performing a kill curve, the next step is to generate a stable cell line by transfection of the parental cell line with a plasmid containing the gene of interest and an antibiotic resistance gene.

    Plasmid DNA Transfection Protocol:
    1. Seed the parental cell line in 24-well plate and incubate for 24h at 37°C.
    2. Transfect the parental cell line the next day at 80% confluency with the construct (e.g. using calcium phosphate etc…) and include a sample of untransfected cells as a negative control. Incubate at 37°C in C02.
    3. After transfection (6h to 24h depending on the transfection method used), wash the cells once with 1X PBS and add fresh medium containing the selection antibiotic to the cells. Use the appropriate antibiotic concentration as determined from the kill curve.
    4. Check, refresh, and expand the cells in selection medium every 2-3 days until you have enough cells for limited dilution (confluency in T25 flask or 10 cm dish).

    Quality Control:
    Seed 24-wells with insert and determine the transfection efficiency by immunostaining:
    1. Grow cells on insert in a 24-well plate until well is confluent.
    2. Remove medium and wash cells with 1X PBS.
    3. Fix cells with methanol or paraformaldehyde and wash with 1X PBS.
    4. Add primary antibody in 24-well against protein of interest and incubate at 37°C for 1 hour (depending on antibody).
    5. Wash cells with 1X PBS.
    6. Add secondary antibody in 24-well and incubate at 37°C for 1 hour depending on antibody).
    7. Wash with 1X PBS.
    8. Remove insert from 24-well plate and affix to microscopy slide with nail polish or other suitable adhesive.
    9. Determine the percentage of transfected cells with fluorescence microscope.


    Selection of Stable Transfected Cell Lines

    Background:
    Once the cells have been successfully transfected, the next step is to seed and select the transfected cell line in a single 96-well plate to select pure colonies by limited dilution as outlined below.

    Protocol:
    1. Seed the transfected cells in 96-well plates in 10% conditioned medium
      • 2x96 well plate with 0.1 cell per well
      • 2x96 well plate with 0.5 cell per well
      • 2x96 well plate with 1 cell per well
    2. Incubate the cells for 24h.
    3. Remove medium and add conditioned selection medium containing selection antibiotic at the pre-determined concentration required for your cell line. Incubate 96-well plates at 37°C with C02.
    4. Check the plates every day for colonies. Colony formation depends on proliferation rate of the cell line and can take anywhere from 3 days to 1 week.
    5. Refresh selective medium every 3-4 days until colonies appear.
    6. Select the wells with only one single colony. Make sure colonies are not growing in clumps as they will be less sensitive to the antibiotic.
    7. When a well contains a single colony, transfer the colony to a 24-well in selection medium and so on until you have enough cells for freezing and storage in liquid nitrogen. Use the appropriate antibiotic concentration as determined from the kill curve.

    Quality Control:
    Seed 24-wells with insert for an immunostaining to determine percentage of cells expressing the gene of interest to be able to identify a 100% pure clone. You can also use Western blotting, flow cytometry or another technique depending on the cell line used.

    Seed 24-wells with insert and determine the expression level of the gene of interest by immunostaining:
    1. Grow cells on insert in a 24-well plate until well has confluent growth.
    2. Remove medium and wash cells with 1X PBS.
    3. Fix cell with methanol or paraformaldehyde and wash with 1X PBS.
    4. Add primary antibody in 24-well plate against protein of interest and incubate at 37°C for 1 hour (depending on antibody).
    5. Wash cells with 1X PBS.
    6. Add secondary antibody in 24-well plate and incubate at 37°C for 1 hour (time depends on antibody type).
    7. Wash cells with 1X PBS.
    8. Remove insert from 24-well plate and affix to microscopy slide with nail polish or other appropriate adhesive.
    9. Determine the percentage of transfected cells with fluorescence microscope.
    MIC Enterobacter| 1 － >64|| Escherichia coli (animal health isolate)| 1 － >64|| Klebsiella| 1 － 32||