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1.16884

Fractogel® EMD DMAE (M)

weak anion exchanger, suspension in 20% ethanol and 150 mM NaCl (40-90 µm)

Synonym(s):

Fractogel® EMD DMAE (M)

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10 mL

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$103.00
100 mL

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$778.00
500 mL

Estimated to ship onMay 06, 2026

$2,730.00
5 L

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UNSPSC Code:
41115711

$103.00


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Quality Level

ligand

diethylaminoethyl

product line

Fractogel®

form

resin

parameter

170 cm/hr flow rate, 8 bar max. pressure

matrix active group

methacrylate

mean particle size

40-90 μm

capacity

100 mg binding capacity (BSA/mg of resin)

transition temp

flash point 35 °C (calculated)

density

1.430 g/cm3

bulk density

1000 kg/m3

application(s)

gene therapy
recombinant protein
vaccine development

separation technique

weak anion exchange

storage temp.

2-30°C

General description

Weak anion exchange Fractogel® resin featuring the tentacle technology, for purification of acidic and neutral proteins and peptides from multiple sources, pDNA purification, DNA, RNA, and endotoxin removal, large viruses purification, vaccine purification, blood fractionation, and more

Features and Benefits

Fractogel® EMD DMAE (M) enables:
  • Excellent binding to large viruses and plasmid DNA
  • Homogenous binding with high selectivity and purity
  • Lower elution volumes for the highest purity levels
  • Compatibility with 2.5 % (v/v) aqueous benzyl alcohol containing 150 mM NaCl storage solution


Due to the titration behavior, the ion exchange capacity can be used from pH 2 to pH 9.5. The separation of proteins is based on reversible electrostatic interactions between the negatively charged regions of the proteins′ surface and the support. Proteins are retained efficiently on Fractogel® EMD DEAE when the pH of the buffer is about 1 unit above their isoelectric points (pl).

The strength of the binding depends on the following:
  • the buffer system
  • pH value of the buffer which determines the surface charge of the protein
  • the degree of the ionization of the functional groups of the exchanger
  • the concentration of the counter ions
  • the charge density on the support (protein binding capacity)

Packaging

  • 1.16884.0100: Fractogel® EMD DMAE (M) Resin 100ml
  • 1.16884.0010: Fractogel® EMD DMAE (M) Resin 10ml
  • 1.16884.0500: Fractogel® EMD DMAE (M) Resin 500ml
  • 1.16884.5000: Fractogel® EMD DMAE (M) Resin 5L

Plastic bottle

Analysis Note

Appearance: Milky, turbid suspension,free from impurities (foreign particles)
Microscopic evaluation: Uniform spherical particles,no agglomerates, no fines
Extractable matter (water): ≤ 0.03 %
Cerium: ≤ 1 µg/g
Pressure drop(column: ID=1.6 cm, L=10 cm at 5 ml/min): ≤ 1.0 bar
Particle size (d10): 37 - 45 µm
Particle size (d50): 48 - 60 µm
Particle size (d90): 63 - 77 µm
Colony forming units (TAMC + TYMC): ≤ 100 CFU/ml
Endotoxins: ≤ 1.00 EU/ml
Protein binding capacity (bovine serum albumin): 80 - 120 mg/ml
Functional test (b:a): ≤ 0.25
Functional test: Separation of conalbumin and human serum albumin

Legal Information

FRACTOGEL is a registered trademark of Merck KGaA, Darmstadt, Germany

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This Item
1.168831.168821.16886
separation technique

weak anion exchange

separation technique

weak anion exchange

separation technique

cation exchange, strong cation exchange

separation technique

cation exchange, weak cation exchange

ligand

diethylaminoethyl

ligand

diethylaminoethyl

ligand

(Sulfoisobutyl)

ligand

carboxymethyl

form

resin

form

resin

form

resin

form

resin

capacity

100 mg binding capacity (BSA/mg of resin)

capacity

100 mg binding capacity (BSA/mg of resin)

capacity

130 mg binding capacity (lysozyme/ml of resin)

capacity

100 mg binding capacity (lysozyme/ml of resin)

matrix active group

methacrylate

matrix active group

methacrylate

matrix active group

methacrylate

matrix active group

methacrylate

product line

Fractogel®

product line

Fractogel®

product line

Fractogel®

product line

Fractogel®


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pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

95.0 °F

flash_point_c

35 °C



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Articles

Learn more one the attenuated viral vaccines manufacturing process: cell culture, clarification, nuclease treatment, chromatography, and sterile filtration.

See case study examples of how to optimize chromatographic purification of plasmid DNA for Biopharmaceutical Applications.

Influenza vaccines are commonly made using egg-based and cell-based manufacturing strategies. Find step-by-step information on the manufacturing process for each method.

View All Articles

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La fabricación de vacunas víricas a medida aborda los retos específicos del virus mediante la colaboración.

This technical article breaks down the adenovirus vaccine manufacturing process and provides a case study on developing an accelerated and cost-effective single-use adenoviral vector vaccine.





Global Trade Item Number

SKUGTIN
116884010004022536741956
116884999904022536718125
116884500004022536168746
116884001004022536595252
116884050004022536168739

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