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cell culture mediumDMEM/F12 Medium

DMEM/F12 Medium

DMEM/F12 culture medium is based on DMEM medium, adding more abundant nutrients in F12 medium, containing a variety of trace elements, which is widely used in the culture of a variety of mammalian cells.

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DMEM/F12 medium is often used as the basis for the development of a serum-free medium, which is suitable for the culture of mammalian cells with low serum content and clonal density culture. The culture medium without glucose can adjust the concentration of glucose at will according to the research needs, convenient and fast.

Ingredients of DMEM/F12 Medium

Cat No.L-GlutamineAlanyl-GlutamineGlucoseHEPESPSPPenicillin-streptomycin Solution
HCY-BCM04001  
HCY-BCM04001A 
HCY-BCM04002   
HCY-BCM04003   
HCY-BCM04003A  
HCY-BCM04004    
HCY-BCM04005   
HCY-BCM04006  
HCY-BCM04007    
HCY-BCM04008     
HCY-BCM04009   
HCY-BCM04010    
HCY-BCM04011    
HCY-BCM04012   
HCY-BCM04013    
HCY-BCM04014   
HCY-BCM04015     
HCY-BCM04016    
HCY-BCM04017     
HCY-BCM04018    
HCY-BCM04019      
HCY-BCM04020     
HCY-BCM04021    
HCY-BCM04022   
HCY-BCM04023     
HCY-BCM04024   

L-glutamine (Glutamine)

L-glutamine (Glutamine) is an essential nutrient element in cell culture, but it is unstable in solution and will degrade spontaneously. The amount of L-glutamine can be arbitrarily adjusted according to the research needs of the medium without L-glutamine, and the addition of fresh L-glutamine or its substitutes at the time of use is more beneficial to the cell growth.

L-alanyl-L-glutamine (Ala-Glu), also known as alanyl-glutamine and alanyl-glutamyl dipeptide, is an advanced cell culture additive that can directly replace L-glutamine in the cell culture medium. l-Glutamine is an essential nutrient in cell culture, but it is unstable in solution and will, however, it is unstable in solution and spontaneously degrades to produce ammonia and pyroglutamic acid, of which ammonia is harmful to cells, whereas L-alanyl-L-glutamine is very stable in aqueous solution and does not degrade spontaneously. The mechanism of cellular utilization is that during cell culture, cells will gradually release a peptidase into the culture medium to hydrolyze L-alanyl-L-glutamyl into L-alanine and L-glutamine, and then cells will take up and utilize these two hydrolysis products. The process of cellular utilization of L-alanyl-L-glutamyl is similar to the flow-addition culture strategy, in that low levels of L-glutamine are continuously added to the culture medium, thereby increasing the utilization of L-glutamine without generating excess ammonia, which is more conducive to cell growth. L-alanyl-L-glutamyl can replace equimolar L-glutamine, is suitable for all cells, requires little adaptation, and can extend the cell culture time. It can also extend the cell culture time and reduce the number of passages, which saves time and money. Cells cultured in medium supplemented with L-glutamine showed a slower reduction in activity than those cultured in a medium supplemented with L-glutamine. The slightly longer delay period is due to the time required for the release of peptidase and digestion of the dipeptide.

HEPES

HEPES is an excellent biological buffer, which has no toxic effect on cells. The medium with HEPES can maintain a constant pH range for a longer period of time, which can effectively prevent the cell growth from being adversely affected by large pH fluctuations of the culture medium. It can be used in CO2-free incubators.

Penicillin-streptomycin Solution

Penicillin-streptomycin solution, also commonly referred to as “dual antibiotics”, is the most commonly used antibiotic in in vitro culture to prevent microbial contamination, in which penicillin interferes with bacterial cell wall synthesis and is particularly effective against Gram-positive bacteria, while streptomycin inhibits bacterial protein synthesis by binding to the 30S subunit of the bacterial ribosome and is particularly effective against Streptomycin binds to the 30S subunit of the bacterial ribosome and inhibits bacterial protein synthesis, which is effective against both Gram-negative and Gram-positive bacteria, but is particularly effective against Gram-negative bacteria. The combination of penicillin and streptomycin can prevent most of the bacterial contamination.

This product contains amino acids, vitamins, inorganic salts and many other components required for multi-culture of cells, but does not contain proteins, lipids or any growth factors, so the product should be used with serum or serum-free additives.

Cautions of IMDM DMEM/F12 Medium

  • This product has been filtered and de-bacterized and should be used with care for aseptic operation to avoid contamination.
  • Do not freeze-thaw the product in order to maintain the best use of the product.
  • This product is intended for scientific research or further study use only, not for diagnosis or treatment.

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