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Roswell Park Memorial Institute medium is commonly known as RPMI. It is a form of medium used in cell culture and tissue culture. This medium contains phosphate and is formulated for use in a 5% carbon dioxide atmosphere. It is used for the growth of human lymphoid cells.
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Roswell Park Memorial Institute medium is commonly known as RPMI. It is a form of medium used in cell culture and tissue culture. This medium contains phosphate and is formulated for use in a 5% carbon dioxide atmosphere. It is used for the growth of human lymphoid cells.
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Dulbecco’s MEM is the most widely used modification of BME. It contains a 4-fold higher concentration of amino acids and vitamins. Non-essential amino acids and certain essential trace elements were added. The bicarbonate concentration was increased. The standard formula for DMEM is with 1000mg/ml glucose. DMEM was originally developed for the culture of mice embryonic cells. Today, it finds a broad application of serum free culture of normal and transformed mouse and chicken cells.
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DMEM (Dulbeccos Modified Eagle Medium) is a widely used basal medium for supporting the growth of many different mammalian cells. Cells successfully cultured in DMEM include primary fibroblasts neurons glial cells HUVECs and smooth muscle cells. We offer a variety of DMEM modifications for a range of cell culture applications. With High GlucoseWithout L-GlutamineWithout Phenol redWithout HEPESManufactured in an ISO 90012015 certified facility.
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Supports cell growth in research and biomanufacturing cell culture processes. Raw material components screened through strict quality control testing for lot-to-lot consistency. Product efficacy and homogeneity tested. Products are hydrated using purified process water and undergo sterile filtration.
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RPMI 1640 is suitable for a wide range of anchorage independent cells. RPMI 1640 Medium is commonly supplemented with 10% Fetal Bovine Serum (FBS). Although RPMI-1640 has been shown to support the serum-free growth of a number of cells.With 2.0 g/L sodium bicarbonateWith HEPES buffer Manufactured in an ISO 90012015 certified facility.
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McCoys 5A Medium is a general purpose medium that supports the propagation of many types of primary cells established cell lines and explants from biopsy tissues. McCoys 5A Medium uses a sodium bicarbonate buffer system (2.2 g/L) and therefore requires a 510% CO2 environment to maintain physiological pH.With L-glutamine phenol red Manufactured in an ISO 90012015 certified facility.
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An acetylated form of L-glutamine; decreases infarct volume and prevents neuronal apoptosis in the substantia nigra in a rat model of MCAO-induced cerebral ischemia-reperfusion injury; prevents decreases in body weight in protein-energy malnourished pigs at 8.28 g/animal per day
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DMEM high glucose liquid media supports cell growth in research upstream process development and cell culture manufacturing processes DMEM high glucose medium efficacy and homogeneity is tested DMEM media contain increased concentrations of vitamins minerals and amino acids compared to traditional basal media DMEM medium composition also includes ferric nitrate making this cell culture medium an option for certain cell lines requiring iron for cell growth DMEM media preparations are available in high or low glucose formulations as well as with or without L-glutamine magnesium and sodium pyruvate DMEM formulation options may also include phenol red as a pH indicator All available DMEM media products contain a sodium bicarbonate buffer with or without HEPES to maintain optimal culture pH DMEM raw material components are screened through strict quality control testing for lot-to-lot consistency DMEM liquid media products are hydrated using purified water and undergo sterile filtra
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Supports cell growth in research and biomanufacturing cell culture processes. Raw material components screened through strict quality control testing for lot-to-lot consistency. Product efficacy and homogeneity tested. Products are hydrated using purified process water and undergo sterile filtration.
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A conditionally essential amino acid; involved in many biochemical processes; synthesized in vivo by glutamate and ammonia; a substrate for the biosynthesis of glutamate and GABA in neurons; decreases adhesion of sickle RBCs to HUVECs when incubated ex vivo with patient-derived autologous plasma either alone or with LPS; commonly used in cell culture media
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