Advanced Basal Medium Eagle (A-BME) in Hanks’ Buffer

  • Advanced Basal Medium Eagle (A-BME) in Hanks’ Buffer

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    Advanced Basal Medium Eagle (A-BME) in Hanks’ Buffer

    Background

    PurMaTM Advanced Basal Medium Eagle (A-BME) in Hanks’ 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. This results in less variation amongst lot-to-lot serum changes. L-alanyl-l-glutamine is the source of glutamine in Advanced BME. Additionally, reducing the requirement for FBS lowers the cost of cell culture experiments.

    Contents

    Advanced BME in HBSS Contains:

    • It includes all twenty essential and non-essential amino acids with higher concentrations than regular and MAX formulations.
    • A-BME incorporates elements to 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 Basal Medium Eagle (A-BME) in Hanks’ Buffer is a significant step toward a chemically defined form of this media. Unquestionably, Chemically Defined Advanced BME (CD-A-BME) is the outcome of decades of cutting-edge research.  Furthermore, it will soon be offered globally to laboratories that are looking for consistency and repeatability in their data.

    Formulation

    The complete formulation can be found here: Advanced BME in Hanks' Buffer (HBSS) Formulation

    References

    1. Improved chemically defined basal medium (CMRL-1969) for primary monkey kidney and human diploid cells. Healy GM, Teleki S, von Seefried A, Walton MJ, Macmorine HG. Appl Microbiol. 1971 Jan;21(1):1-5. doi: 10.1128/am.21.1.1-5.1971. PMID:
    2. Nutritional requirements for the production of herpes simplex virus. I. Influence of glucose and glutamine of herpes simplex virus production by HeLa cells. LEWIS VJ Jr, SCOTT LV. J Bacteriol. 1962 Mar;83(3):475-82. doi: 10.1128/jb.83.3.475-482.1962. PMID: 14464909
    [/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
  • Advanced Minimum Essential Media (A-MEM) in HBSS

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    Advanced Minimum Essential Media (A-MEM) in Hanks’ Buffer

    Background

    PurMaTM Advanced Minimum Essential Media (A-MEM) in Hanks’ 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 A-MEM. Additionally, reducing the requirement for FBS lowers the cost of cell culture experiments.

    Contents

    Advanced MEM in HBSS Contains:

    • includes all twenty essential and non-essential amino acids with higher concentrations than regular and MAX formulations.
    • A-MEM 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 Minimum Essential Media (A-MEM) in Hanks’ Buffer is a significant step toward a chemically defined form of this media. Unquestionably, Chemically Defined Advanced MEM (CD-A-MEM) 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 (HBSS) Formulation in Hanks' Buffer 

    References

    1. Myelin formation in rat dorsal root ganglion cultured in a serum-free medium. Ninomiya T, Takahashi K. J Anat. 1987 Jun;152:209-13. PMID: 3654371
    2. Long-term organ culture of hamster cheek pouch mucosa. Mock D, Main JH. J Oral Pathol. 1976 Jul;5(4):237-40. doi: 10.1111/j.1600-0714.1976.tb01770.x. PMID: 820846
    [/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
  • Hanks’ Balanced Salt Solution (HBSS)

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    Hanks’ Balanced Salt Solution (HBSS)

    Background

    Hanks’ Balanced Salt Solution (HBSS) contains inorganic salts and glucose. HBSS for a short time provides an ideal environment to preserve the structural and physiological integrity of cells in vitro. HBSS maintains a balance between intra and extracellular osmolarity, delivers water and inorganic ions necessary for cell metabolism, and provides energy for cellular metabolism with glucose.

    Grades of Hanks’ Balanced Salt Solution (HBSS)

    Regular Grade Buffer

    PurMa Biologics manufactures Regular grade of buffer by using:  PurMa™ Cell Culture Suited Water (Cat# P3W110101) we finally sterilize the buffers by autoclaving the solution and packing  in our Class 100 Aseptic Facility.

    Cell Culture Suited Grade Buffer

    PurMa Biologics manufactures this grade of buffer by using :PurMa™ Cell Culture Suited Water (Cat# P3W110101) In our Class 100 Aseptic Facility we Buffer will finally sterilize the buffer by 0.2 µm filter and pack under N2

    RNase and DNase Free Grade Buffer

    PurMa Biologics manufactures this grade of buffer by using :PurMa™ Cell Culture Suited Water (Cat# P3W120103) In our Class 100 Aseptic Facility we Buffer will finally sterilize the buffer by 0.2 µm filter and pack under N2

    Cell Culture Suited / Endotoxin Depleted Grade Buffer

    PurMa Biologics manufactures this grade of buffer by using: PurMa™ Ultra-Pure Cell Culture Suited Water (Cat# P3W110102) In our Class 100 Aseptic Facility we Buffer will finally sterilize the buffer by 0.1 µm filter and pack under N2

    The Endotoxin Removing Procedure from Buffer

    PurMa biologics has the most sophisticated endotoxin removal. For that we pass the buffer  through the PurMaTM Endotoxin Elimination Column (Cat# P6H1216251). Furthermore, in our proprietary column we covalently conjugate Sepharose 6B   to an endotoxin-specific absorbent. we finally  eliminate the residual endotoxin by passing the unbound fraction three times through 0.1µm filters.

    General Features

    • It is cost effective.
    • Cell Culture Suited
    • Provides  maintenance  and  integrity for  cells or tissues during irrigation, transportation, or dilution.
    • To wash and re-suspend cells during the dissociation or counting process (Ca+2, Mg+2 free)
    • PurMa Biologics offers HBSS in three pH formats, pH 7.2, 7.4, and pH 7.6.

    Specific Features

    • Glucose maintains the intra and extracellular osmotic pressure as well as provides the principal source of energy for cellular metabolism.
    • HBSS Provides water and important inorganic ions necessary for cellular metabolism.
    • This buffer Provides a buffer solution to maintain a medium in physiological pH (7.2-7.6)
    • It is made in Mg2+ and Ca 2+-free water.
    • Free of RNAse /DNase
    • Free of Proteases. It is rigorously tested for contaminating nonspecific endonuclease, exonuclease, and RNase activity.
    • It is rigorously tested for contamination of endotoxin and mycoplasma.
    • Is manufactured in three pH: 7.2 ± 0.01, pH: 7.4 ± 0.01, and 7.6 ± 0.01 at 25°C.
    • Sterile filtered by 0.22µm membrane (in case of endotoxin-depleted buffer by 0.1µm)
    • As it is packed under N2, the pH won’t change over time before opening the bottle.

    Application

    This buffer especially has an excellent role in protocols requiring the use of consistent conditions such as crosslinking, biotinylation, and fluorescent labeling reactions which require an amine-free buffer.

    Formulation

    For complete formulation, click here:HBSS Formulation

    References

    1. Relation of oxygen and temperature in the preservation of tissues by refrigeration. Hanks, j. h., Wallace, r. e., 1949, Proc Soc Exp Biol Med. 1949 Jun;71(2):196-200. doi: 10.3181/00379727-71-17131.
    2. Isolation and purification of Giardia trophozoites from rat intestine. Feely DE, Erlandsen SL. J Parasitol. 1981 Feb;67(1):59-64. PMID: 7229820 .
    3. Selective recovery of living microfilariae from Onchocerca volvulus nodules. Determination of optimal conditions for their culture in vitro for excretory/secretory products. Ngu JL, Neba GA, Leke N, Titanji V, Asonganyi T, Ndumbe P. Acta Trop. 1981 Sep;38(3):261-6. PMID: 611803
    [/fusion_text][fusion_table fusion_table_type="1" 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  6.7 ± 0.01; 7.0 ± 0.01; 7.4 ± 0.01; 7.8 ± 0.01
    Osmolality  275-360 mOsm/L
    Endotoxin  NMT< 2EU/mL
    Mycoplasma Negative
    Suitability  Suitable for mammalian cell culture
    Additive  N/A
    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 1 Gallon, 6 X 1 Gallon Read more

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