MEM Alpha Modification in Earle’s Buffer (MEM-α)

  • Advanced MEM Alpha-Modification (A-MEM-α) in Earle’s Buffer

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    Advanced MEM Alpha-Modification (A-MEM-α) in Earle’s Buffer

    Background

    PurMaTM Advanced MEM Alpha-Modification (A-MEM-α) in Earle’s Buffer contains components to provide a 60–90% reduction in FBS supplementation. More importantly, using synthetic components such as recombinant insulin, albumin, and transferrin increases consistency. Consequently, this results in less variation amongst lot-to-lot serum changes. L-alanyl-l-glutamine is the source of glutamine in Advanced MEM-α. Additionally, reducing the requirement for FBS lowers the cost of cell culture experiments.

    Contents

    Advanced MEM-α in EBSS Contains:

    • includes all twenty essential and non-essential amino acids with higher concentrations than regular and MAX formulations.
    • A-MEM-α incorporates elements that significantly reduce the need for a serum for cell culture.

    Crucial Ingredients:

    • PurMaTM Human Transferrin (Holo): prevents improper iron storage and delivery in cell culture systems which is a major contributor to oxidative stress and protein damage.
    • PurMaTM Insulin Recombinant
    • Trace of other elements which mimic the elements in fetal bovine serum.
    Consequently, Advanced MEM Alpha-Modification (A-MEM-α) in Earle’s Buffer is a significant step toward a chemically defined form of this media. Unquestionably, Chemically Defined Advanced MEM-α (CD-A-MEM-α) is the outcome of decades of innovative cutting-edge research and will soon be offered globally to laboratories that are looking for consistency and repeatability in their data.

    Formulation

    Complete formulation is available here: Advanced MEM-alpha in Earle's Buffer 

    References

    1. The growth of L-cells and Vero cells on an autoclavable MEM-peptone medium. L Keay Biotechnology and bioengineering, 19(3), 399-411 (1977-03-01).
    2. Minimum essential medium alpha (MEM) enhances assisted reproductive technology results. I. Mouse embryo study. Wun WS, Wun CC, Grunert GM. J Assist Reprod Genet. 1994 Jul;11(6):303-7. doi: 10.1007/BF02215717. PMID: 7734915.
    3. Alpha-minimum essential medium (MEM) enhances in vitro hatched blastocyst development and cell number per embryo over Ham's F-10. Roudebush WE, Often NL, Butler WJ. J Assist Reprod Genet. 1994 Apr;11(4):203-7. doi: 10.1007/BF02211809. PMID: 7711383.
    [/fusion_text][fusion_table fusion_table_type="2" fusion_table_rows="13" fusion_table_columns="2" margin_top="30px" margin_right="" margin_bottom="" margin_left="" hide_on_mobile="small-visibility,medium-visibility,large-visibility" class="" id="" animation_type="" animation_direction="left" animation_color="" hue="" saturation="" lightness="" alpha="" animation_speed="0.3" animation_delay="0" animation_offset=""]
    Parameter Specification
    Appearance Red, clear liquid
    pH 7.2 ± 0.1
    Osmolality 275-360 mOsm/L
    Endotoxin NMT< 2EU/mL
    Mycoplasma Negative
    Suitability  Suitable for mammalian cell culture
    Additive Sodium pyruvate
    Indicator Phenol red
    Mycoplasma Detection Negative
    Sterility Tested Sterile filtered using 0.22 µm filter
    Form Liquid
    Shipping Condition  Room temperature
    [/fusion_table][/fusion_builder_column][/fusion_builder_row][/fusion_builder_container]1 x 500 ml, 6 x 500 ml, 1 x 1000 ml, 6 x 1000 ml, 1 x 10 L, 1 x 50 L, 10 X 1EZ Individually Packed, 50 X 1EZ Individually Packed Read more
  • MEM Alpha Modification in Earle’s Buffer (MEM-α)

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    MEM Alpha Modification in Earle’s Buffer (MEM-α)

    Background

    MEM Alpha Modification in Earle’s Buffer (MEM-α) is certainly a suitable nutrient for mammalian cell culture as well as selection for transfected DHFR-negative cells. MEM -α Modification is widely used for primary osteoblast cultures as well as isolation of polymorphonuclear leukocytes (PMN) from umbilical cord blood. Eliminating calcium in this media facilitates the growth of cells in suspension cultures.

    MEM -α  contains

    • Non-essential amino acids.
    • Sodium pyruvate.
    • Lipoic acid.
    • Vitamin B12.
    • Biotin and,
    • Ascorbic acid.
    • Also, MEM-α does not contain deoxyribonucleosides and ribonucleosides.
    • Moreover, PurMaTM MEM -α media in Earle's buffer includes Earles’ buffer

    The composition of Earle's buffer, it contains:

    1. Calcium chloride
    2. Magnesium sulfate
    3. Potassium chloride
    4. Sodium bicarbonate
    5. Sodium chloride
    6. Sodium Phosphate, monobasic

    Additionally, MEM Alpha Modification in Earle’s Buffer (MEM-α)

    it contains:
    • Low level of glucose (1.00 g/ liter)
    • More importantly, Sodium bicarbonate (2.2 g/L) (if higher than 5% CO2 is used, a higher % of sodium bicarbonate is needed.
    • 2 mM L-glutamine (292 mg/L)’
    • Also, PurMa Biologics manufactures 118 types of MEM-α

    Application

    This media can also be used with a variety of suspension and adherent cells including keratinocytes, primary rat astrocytes as well as human melanoma cells. Furthermore, Alpha modification of Minimum Essential Medium Eagle has also been used for the isolation of mesenchymal stem cells, adipose-derived stem cells, and osteoblast.

    Why PurMa Biologics? Why we stand behind our cell culture media.

    Our products are the outcome of 30 years of experience in cutting edge science. We routinely manufacture over 1500 media. We have the most comprehensive collection of cell and tissue culture media. Moreover, we utilize %99 pure amino acids. This will significantly increase the consistency among your experiments. Considering the highest quality, our prices certainly are extremely reasonable.

    Formulation

    Complete formulation is in the " Formulation tab" as well as here: MEM-alpha Formulation in Earle's Buffer

    References

    1. The growth of L-cells and Vero cells on an autoclavable MEM-peptone medium. Keay et al.  Biotechnology and bioengineering, 19(3), 399-411 (1977-03-01).
    2. Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction. Maharaj et al. The Journal of steroid biochemistry and molecular biology, 202, 105730-105730 (2020-07-20)
    [/fusion_text][fusion_table fusion_table_type="2" fusion_table_rows="13" fusion_table_columns="2" margin_top="30px" margin_right="" margin_bottom="" margin_left="" hide_on_mobile="small-visibility,medium-visibility,large-visibility" class="" id="" animation_type="" animation_direction="left" animation_color="" hue="" saturation="" lightness="" alpha="" animation_speed="0.3" animation_delay="0" animation_offset=""]
    Parameter Specification
    Appearance Red, clear liquid
    pH 7.2 ± 0.1
    Osmolality 275-360 mOsm/L
    Endotoxin NMT< 2EU/mL
    Mycoplasma Negative
    Suitability  Suitable for mammalian cell culture
    Additive Sodium pyruvate
    Indicator Phenol red
    Mycoplasma Detection Negative
    Sterility Tested Sterile filtered using 0.22 µm filter
    Form Liquid
    Shipping Condition  Room temperature
    [/fusion_table][/fusion_builder_column][/fusion_builder_row][/fusion_builder_container]1 x 500 ml, 6 x 500 ml, 1 x 1000 ml, 6 x 1000 ml, 1 x 10 L, 1 x 50 L, 10 X 1EZ Individually Packed, 50 X 1EZ Individually Packed Read more
  • MEM Alpha-Modification MAX in Earle’s Buffer (MEM-α-MAX)

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    MEM Alpha-Modification MAX (MEM-α-MAX) in Earle’s Buffer

    Background

    MEM Alpha-Modification MAX (MEM-α-MAX) in Earle’s Buffer is a commonly used media for Mammalian cell culture.

    Advantages

    MEM-α performs better than MEM for a number of cell lines, please see the description of regular MEM-α: MEM-a in Earle's Buffer

    The advantages of MEM-α-MAX in EBBS over MEM-α are:

    • Higher PH Capacity
    • Moreover, it contains 4 mM L-Alanyl-L-Glutamine (0.869 g/L) instead of L-Glutamine and therefore:
    • Possess longer shelf life.
    • More importantly, minimizes toxic ammonia build-up.
    • Significantly improves cell viability and growth.
    • Remains stable across a wide range of temperatures.
    • Improves the culture of primary cells.

    Mechanism

    Although L-glutamine is a vital amino acid, it degrades, generating toxic ammonia and pyrrolidine carboxylic acid. One way to minimize L-glutamine degradation in media is to gradually add these amino acids to your cell culture. However, keeping track of time to keep the amount of L-glutamine at the same level is tedious, if not impossible. Alternatively, L-alanyl-L-glutamine can be used because it is much more stable in aqueous solutions. More importantly, it does not easily degrade and gradually releases aminopeptidases. As a result, L-glutamine and L-alanine are then used by the cells for protein production in the TCA cycle. In addition to our Max formulation products, we manufacture PurMaTM GluaSup (Cat# P3S210 559) is a combination of L-alanyl-L-glutamine that prevents the degradation of L-glutamine.

    Contents

    MEM Alpha-Modification MAX (MEM-α-MAX) in Earle’s Buffer contains:

    • 5 mM sodium pyruvate
    • High glucose (4.5g/L)
    • Non-Essential Amino Acids
    • 3.7 g/L Sodium Bicarbonate; PurMa Biologics Manufactures several types of MEM-α-MAX based on the amount of Sodium Bicarbonate and HEPES (PH capacity)
    • Phenol Red
    MEM-α-MAX in EBBS contains no proteins, lipids, or growth factors. Therefore, it requires supplementation, commonly with 10% Fetal bovine Serum (FBS).

    Formulation

    The complete formulation can be found here: MEM-alpha-MAX Formulation in Earl's Buffer

    References

    1. The growth of L-cells and Vero cells on an autoclavable MEM-peptone medium. L Keay Biotechnology and bioengineering, 19(3), 399-411 (1977-03-01).
    2. Minimum essential medium alpha (MEM) enhances assisted reproductive technology results. I. Mouse embryo study. Wun WS, Wun CC, Grunert GM. J Assist Reprod Genet. 1994 Jul;11(6):303-7. doi: 10.1007/BF02215717. PMID: 7734915.
    3. Alpha-minimum essential medium (MEM) enhances in vitro hatched blastocyst development and cell number per embryo over Ham's F-10. Roudebush WE, Often NL, Butler WJ. J Assist Reprod Genet. 1994 Apr;11(4):203-7. doi: 10.1007/BF02211809. PMID: 7711383.
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    Parameter Specification
    Appearance Red, clear liquid
    pH 7.2 ± 0.1
    Osmolality 275-360 mOsm/L
    Endotoxin NMT< 2EU/mL
    Mycoplasma Negative
    Suitability  Suitable for mammalian cell culture
    Additive Sodium pyruvate
    Indicator Phenol red
    Mycoplasma Detection Negative
    Sterility Tested Sterile filtered using 0.22 µm filter
    Form Liquid
    Shipping Condition  Room temperature
    [/fusion_table][/fusion_builder_column][/fusion_builder_row][/fusion_builder_container]1 x 500 ml, 6 x 500 ml, 1 x 1000 ml, 6 x 1000 ml, 1 x 10 L, 1 x 50 L, 10 X 1EZ Individually Packed, 50 X 1EZ Individually Packed Read more

MEM Alpha Modification in Earle’s Buffer (MEM-α)

Background

MEM Alpha Modification in Earle’s Buffer (MEM-α) certainly suits mammalian cell culture as well as selection for transfected DHFR-negative cells. MEM -α Modification applies for primary osteoblast cultures as well as isolation of polymorphonuclear leukocytes (PMN) from umbilical cord blood. Eliminating calcium in this media facilitates the growth of cells in suspension cultures.

MEM -α  contains

  • Non-essential amino acids.
  • Sodium pyruvate.
  • Lipoic acid.
  • Vitamin B12.
  • Biotin and,
  • Ascorbic acid.
  • Also, MEM-α does not contain deoxyribonucleosides and ribonucleosides.
  • Moreover, PurMaTM MEM -α media in Earle’s buffer includes Earles’ buffer

The composition of Earle’s buffer, it contains:

  1. Calcium chloride
  2. Magnesium sulfate
  3. Potassium chloride
  4. Sodium bicarbonate
  5. Sodium chloride
  6. Sodium Phosphate, monobasic

Additionally, MEM Alpha Modification in Earle’s Buffer (MEM-α)

it contains:

  • Low level of glucose (1.00 g/ liter)
  • More importantly, Sodium bicarbonate (2.2 g/L) (if higher than 5% CO2 is used, a higher % of sodium bicarbonate is needed.
  • 2 mM L-glutamine (292 mg/L)’
  • Also, PurMa Biologics manufactures 118 types of MEM-α

Application

This media can also be used with a variety of suspension and adherent cells including keratinocytes, primary rat astrocytes as well as human melanoma cells. Furthermore, Alpha modification of Minimum Essential Medium Eagle has also been used for the isolation of mesenchymal stem cells, adipose-derived stem cells, and osteoblast,

We stand behind our cell culture media.

Our products are the outcome of 30 years of experience in cutting-edge science. PurMa Biologics manufactures over 1500 media. We have the most comprehensive collection of cell and tissue culture media. Moreover, we use %99 pure amino acids. This will significantly increase the consistency of your experiments. Considering the highest quality, our prices certainly are extremely reasonable.

Formulation

Complete formulation is in the ” Formulation tab” as well as here: MEM-alpha Formulation in Earle’s Buffer

References

  1. The growth of L-cells and Vero cells on an autoclavable MEM-peptone medium. Keay et al.  Biotechnology and bioengineering, 19(3), 399-411 (1977-03-01).
  2. Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction. Maharaj et al. The Journal of steroid biochemistry and molecular biology, 202, 105730-105730 (2020-07-20)

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