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DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate 500ml

DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate 500ml

DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate 500ml

$14.00

DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate 500ml

$14.00

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High-Quality Classical Media for Optimal Cell Culture

Partnering with Biowest, we offer a comprehensive selection of trusted media formulations, including Dulbecco’s Modified Eagle Medium (DMEM), Eagle’s Minimum Essential Medium (EMEM), RPMI 1640, and Ham’s F-12. Our products are meticulously manufactured in state-of-the-art ISO certified facilities to ensure consistent quality and reliability.

Key Features:

  • Low Glucose w/ L-Glutamine w/ Sodium Pyruvate
  • Versatile formulations: Choose from a variety of classical media to suit your specific cell culture needs.
  • Proven performance: Compatible with a wide range of cell lines, including those from ATCC, DSMZ, and Riken.
  • Exceptional quality: Manufactured in ISO 9001:2008 and ISO 13485:2012 certified facilities.
  • Extended shelf life: Sterile-filtered media with a 12-month shelf life for convenience.
  • Trusted by leading institutions: Widely used in renowned research centers like NUS and CSI in Singapore.

** please inquiry for powdered formulation

Please enquire with us at [email protected]

We deliver Biowest solutions across South East Asia (Singapore, Thailand, Vietnam, Indonesia, Philippines, Myanmar) and Across China Only.

Documents

MSDS

Technical Data Sheet

Composition

Testimonials

Biowest DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate (L0060-500) Used For Scratch Wound Assay

Wound healing assays (Scratch wound assay) are widely utilized in cancer research and studies of cell-cell interactions to investigate cell migration, particularly in the context of skin wound repair and cancer metastasis. In this method, a confluent monolayer of cells is mechanically scratched to create a “wound,” and the rate of closure is monitored over time.

In the experiment, HaCaT were routinely cultured Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS). All cells were cultured in a 37 degree Celsius, 5% carbon dioxide, humidified incubator. keratinocytes were routinely sub-cultured using 0.25 % trypsin and 1 mM Ethylenediaminetetraacetic acid. A linear scratch wound were created on a confluent layer of seeded cells and were treated in DMEM low glucose in the absence or presence of 10% FBS for 8 hours. Images were captured at regular intervals to analyse the wound closure over time.

A linear scratch wound were created on a confluent layer of seeded cells and were treated in DMEM low glucose in the absence or presence of 10% FBS for 8 hours. Images were captured at regular intervals to analyse the wound closure over time.

 

Materials:

 

 

Biowest DMEM Low Glucose w/ L-Glutamine w/ Sodium Pyruvate (L0060-500) Used For 3D In-vitro Skin

The EU has banned animal testing for cosmetics and their ingredients since 2013. A growing demand for in vitro skin models has been rising steadily to cater for both the safety testing (Skin irritation) and efficacy testing (functional test).

In the experiment, primary keratinocytes were seeded on a cultured insert to form a confluent layer. The confluent layer of cells is lifted to an air-liquid interface for 14 days to stimulates the keratinocytes to differentiate (stratification) and form a multi-layered epidermis that contains stratum corneum layers. The specialized medium primarily used consists of DMEM and Ham’s F12 in a specific ratio. It is chemically defined and serum-free to ensure a high reproducibility in result. Treatments can be topically applied to the skin model for a period of times. Histology such as H&E staining and other skin markers are commonly carried out. Gene expression and protein study are also alternative analysis method.

In the experiment, primary keratinocytes were seeded on a cultured insert to form a confluent layer. The confluent layer of cells is lifted to an air-liquid interface for 14 days to stimulates the keratinocytes to differentiate (stratification) and form a multi-layered epidermis that contains stratum corneum layers.
Fig 2. H&E Histology staining of 3D reconstructed human skin

 

Materials:

Reference Publications

Sandhiutami, N. M., Moordiani, M., Laksmitawati, D. R., Fauziah, N., Maesaroh, M., & Widowati, W.

In vitro assesment of anti-inflammatory activities of coumarin and Indonesian cassia extract in RAW264.7 murine macrophage cell line.

Iranian journal of basic medical sciences20(1), 99–106. (2017). 

DOI: https://doi.org/10.22038/ijbms.2017.8102

Article Snippet:Cells were grown in Dulbecco’s Modified Eagle Medium (DMEM, Biowest L0060) supplemented with contain 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin (Biowest L0022-100), and then incubated at 37 °C and 5% CO2 until the cells were confluent.”

 

 

Victoria-Escandell, A., Ibañez-Cabellos, J. S., De Cutanda, S. B., Berenguer-Pascual, E., Beltrán-García, J., García-López, E., Pallardó, F. V., García-Giménez, J. L., Pallarés-Sabater, A., Zarzosa-López, I., & Monterde, M.

Cellular Responses in Human Dental Pulp Stem Cells Treated with Three Endodontic Materials

Stem Cells International2017, 1–14. (2017).

DOI: https://doi.org/10.1155/2017/8920356

Article Snippet: Briefly explained, 100 mg of each freshly mixed RCS (AH-Plus and MTA-Fillapex) and 100 mg of MTA-Angelus powder were immersed in 1 mL of serum-free low-glucose DMEM (Biowest, ref: L0060-500), supplemented with antibiotics and fungicides.”

 

Unlu, A., Bulbul, M. V., Erkan, B. K., Ozdemir, İ., Keskin, I., & Sutcu, M. 

Examination of the effect of xenogeneic mesenchymal stem cells and conditioned medium on cartilage graft viability: a rabbit model.

Archives of Aesthetic Plastic Surgery29(3), 129–135. (2023).

DOI: https://doi.org/10.14730/aaps.2022.00773

Article Snippet: For the culture of canine-derived ADMSCs, low-glucose Dulbecco serum supplemented with 15% fetal bovine serum (F7524; Sigma Aldrich), 2% L-glutamine (G6392; Sigma Aldrich) and 1% antibiotic-antimycotic solution (A5955; Sigma Aldrich) modified Eagle’s medium (L0060; Biowest) medium was used.”