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Save your lab’s valuable cold storage space with Gibco BenchStable Media, engineered for flexibility and convenience, this media enables storage at room temperature. BenchStable Media is available in the most commonly used basal media formulations: DMEM, DMEM/F-12, MEM, and RPMI 1640. These media have been optimized for routine cell culture, maintaining expected morphology and function of many common cell lines.
Explore the benefits of BenchStable Media:
BenchStable Media have more sustainable packaging and help reduce energy consumption by promoting the efficient use of cold storage when compared to traditional media.
Globally, a switch by scientists to BenchStable Media from current refrigerated media would save 34 GWh of energy each year, equivalent to the yearly greenhouse gas (GHG) emissions from more than 5,000 passenger cars.
BenchStable Media is packaged in a Gibco bottle made from PET with HDPE lid—two of the most highly recycled plastics. The media bottle comes in protective packaging, a paperboard box made from 100% recyclable material, to prevent degradation from light exposure.
While the paperboard box is added packaging, it contributes 0.05 lb of CO2 equivalents compared with the 6.5 lb of CO2 equivalents saved by enabling ambient media storage, resulting in a 6.45 lb of CO2 equivalents benefit with a switch to BenchStable Media.
Figures 1 and 2 show that BenchStable Media support cellular growth rates equivalent to those observed in conventional media. Figures 3, 4, and 5 show that cell functionality, including morphology and health, is maintained in BenchStable Media.
Figure 1. BenchStable Media support equivalent growth rates in long-term cultures. HeLa (MEM; pink), HEK293 (DMEM; blue), Jurkat (RPMI; green), and SH-SY5Y (DMEM/F-12; yellow) cells were grown in standard (closed points) and BenchStable (open points) media supplemented with 10% FBS for 15 passages. Cell counts at each passage were used to calculate population doubling times.
Figure 2. BenchStable Media support equivalent growth rates in short-term cultures. A549 (MEM; pink), MCF7 (DMEM; blue), THP-1 (RPMI; green), and CHO-K1 (DMEM/F-12; yellow) cells were grown in standard (closed points) and BenchStable (open points) media supplemented with 10% FBS for 5 passages. Cell counts at each passage were used to calculate population doubling times.
Figure 3. BenchStable DMEM supports HEK293 cell culture. HEK293 human embryonic kidney cells were cultured for 15 passages in DMEM (left; Cat. No. 10566016) or BenchStable DMEM (right; Cat. No. A4192101) supplemented with 10% FBS. Images were captured at passage 15 using 10x magnification on an EVOS FL Auto Imaging System.
Figure 4. BenchStable DMEM supports HeLa cell culture. HeLa human cervical adenocarcinoma cells were cultured for 15 passages in MEM (left; Cat. No. 41090036) or BenchStable MEM (right; Cat. No. A4192201) supplemented with 10% FBS. Images were captured at passage 15 using 10x magnification on an EVOS FL Auto Imaging System.
Figure 5. Cells cultured in BenchStable Media maintain healthy mitochondria. HeLa cells cultured in DMEM (left) and BenchStable DMEM (right) for eight passages were stained with tetramethylrhodamine methyl ester (TMRM; Cat. No. T668) and Hoechst 33342 Solution (Cat. No. 62249). TMRM is a cell-permeant dye that accumulates in active mitochondria, resulting in a bright signal in healthy cells.
BenchStable Media are reliable for your cell culture applications. Figure 6 shows that transfection efficiency remains high for cells cultured in BenchStable Media. Figure 7 shows that cells cultured in conventional media and cells cultured in BenchStable Media exhibit comparable gene expression levels.
Figure 6. Equivalent transfection efficiency in BenchStable Media cultures. HeLa cells cultured in MEM (left) and BenchStable MEM (right) for over five passages were transfected with a GFP-containing plasmid DNA via Lipofectamine 3000 (Cat. No. L3000015). Transfection efficiency was measured in cells harvested 24 h post-transfection by analysis on the Attune NxT Flow Cytometer, using untransfected cells as negative control.
Figure 7. Effective differentiation in BenchStable Media SH-SY5Y cultures. SH-SY5Y neuroblastoma cells cultured in DMEM/F-12 (left panels) and BenchStable DMEM/F-12 (right panels) were treated with 10 µM retinoic acid and allowed to differentiate for five days. Cells were stained with Alexa Fluor 488 phalloidin (green; Cat. No. A12379) and Hoechst 33342 Solution (blue; Cat. No. 62249) to allow visualization of extended, branched neuron-like processes (top panels). Cholinergic neuron-like phenotypes (bottom panels) were shown by staining parallel cultures for tubulin (red; Cat. Nos. MA1-118x and A11005 for primary and secondary antibody) and choline acetyl transferase (ChAT, green; Cat. Nos. PA1-4738 and A11034 for primary and secondary antibodies).
In creating this next innovation in cell culture media, we took great care to help ensure BenchStable Media will provide the quality and consistency that you rely on. Figure 8 shows the negative impact light has on all standard media and is the reason behind the protective packaging. Figure 9 illustrates that essential vitamin and amino acid levels are consistently maintained in BenchStable Media stored at ambient room temperatures.
Figure 8. Light exposure alters media performance. DMEM/F-12 regularly exposed to standard laboratory light was supplemented with 10% FBS and used to culture HEK293 cells over a period of four weeks. After 25 days of light exposure HEK293 growth rates were significantly reduced. Images were taken approximately 95 hours after plating HEK293 cells at P7.
Figure 9. Media components remain consistent in BenchStable Media. BenchStable RPMI (left) and BenchStable DMEM/F-12 (right) media were maintained at room temperature (20–25°C) for 13 months. Samples taken at 1, 2, 3, 5, 7, 9, and 13 months were assessed for vitamin and amino acid concentrations via HPLC and compared with concentrations in lot-matched media stored at 2–8 °C.
Jane L. Tarry-Adkins, India G. Robinson, Rebecca M. Reynolds, Irving L. M. H. Aye, D. Stephen Charnock-Jones, Benjamin Jenkins, Albert Koulmann, Susan E. Ozanne and Catherine E. Aiken. Front Cell Dev Biol, 17 June 2022. PMID: 35784487.
Chloe E. Spencer, Stephen Rumbelow, Steve Mellor, Catherine J. Duckett, and Malcolm R. Clench. Pharmaceutics 2022, 14(2), 364. PMID: 35214096
Watch these videos to learn how you can break through your lab's limitations in cold-storage space with BenchStable Media.
These highly purified, recombinant enzymes provide fast yet gentle cell dissociation. Ideal for dissociating attachment-dependent cell lines, TrypLE reagents can be directly substituted for trypsin without protocol changes.
Extend the life of your cells with GlutaMAX supplement. GlutaMAX supplement is stable in aqueous solutions and does not spontaneously degrade. This improved cell culture supplement can be used as a direct substitute for L-glutamine in your cell culture media.
Add new room temperature stable BenchStable Media to your Supply Center to save refrigerator space. These innovative media are available in the most commonly used formulations: DMEM, DMEM/F-12, MEM, and RPMI 1640.
Do you need more information about using BenchStable Media in your cell culture experiments? Get your answers by visiting our FAQs for BenchStable Media.
Gibco cell culture products are manufactured in facilities compliant with current good manufacturing practices (GMP) and adhere to a robust quality management system, helping to ensure the consistency, reliability, and high quality you can rely on.
We are committed to delivering products that serve the research needs of our customers, while striving to develop them in a way that minimizes our use of natural resources and our impact on the environment.
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