![]() |
Technical Data
Media
|
|
MEM Eagle w/Earle’s, w/o L-Glutamine, amino acids (Powder)
M3859-01
Cell Culture Grade
Storage RT/4°C Shipping RT
|
Components shown as g/liter
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Minimum Essential Medium (MEM was, developed by Harry Eagle. It is one of the most widely used of all synthetic cell culture media. Early attempts to cultivate normal mammalian fibroblasts and certain subtypes of HeLa cells revealed that these types of cells had specific nutritional requirements that could not be met by Eagle's Basal Medium (BME). Studies using these and other cells in culture indicated that additions to BME could be made to aid growth of a wider variety of fastidious cells. MEM incorporates these modifications which includes higher concentrations of amino acids so that the medium more closely approximates the protein composition of mammalian cells. MEM has been used for cultivation of a wide variety of cells grown in monolayers. Optional supplementation of non-essential amino acids to the formulations that incorporate either Hanks' or Eagles' salts has broadened the usefulness of this medium. Directions per Liter: Dissolve 8.70 grams in 900 mL of distilled/deionized (DDI) water, stirring gently until completely solubilized. Do NOT heat. If required, add 2.2g sodium bicarbonate with stirring. Adjust pH of the medium to 0.1-0.3 pH units below the desired pH. Filter-sterilize using a 0.22 micron membrane. Add additional water to bring the solution to final volume. Aliquot into sterile containers. Storage and Stability: Store powdered media at RT. Opened bottles should be capped tightly and kept in a dark, low humidity environment. Prepared media should be kept at 4°C and used within a short period of time. Appearance: Light orange, homogenous, free flowing powderSolubility Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
1. Eagle, H., Tissue Culture Association Manual 3: 517-520 (1976). 2. Eagle, H., Science 122: 501 (1955). |