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Merck
CN

76153

PEGA resin

extent of labeling: ~0.4 mmol/g loading

Synonym(s):

Poly[acryloyl-bis(aminopropyl)polyethylene glycol]

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About This Item

UNSPSC Code:
23151817
NACRES:
NA.22
MDL number:
MFCD00165212

Key Documents

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Product Name

PEGA resin, extent of labeling: ~0.4 mmol/g loading

product line

PEGA

form

crystals

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

extent of labeling

~0.4 mmol/g loading

impurities

90% methanol

particle size

150-300 μm

functional group

amine

Quality Level

100

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Application

Polyacrylamide resin possessing long polyethylene glycol spacers giving extremely high swell resin may be used for:
  • immobilizing enzymes in aqueous solution
  • affinity purification of small-molecule binding proteins
  • synthesis of peptide libraries with fluorescently labeled proteins

General description

PEGA resins are a hydrophilic acrylamide-PEG co-polymer providing a really extensive and more uniform swelling in a wide range of solvents (from water, methanol, ethanol to tetrahydrofuran, acetonitrile and toluene). The extreme swelling volume of this support in the standard peptide synthesis solvents DCM and DMF together with their good stability make them ideally suited for the batch as well as for continuous-flow syntheses.

Packaging

Sold on basis of weight of dry resin.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM8662
BCBP4861V
1381725V
1381725
1313432

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Identification of small molecule binding molecules by affinity purification using a specific ligand immobilized on PEGA resin.
Kuramochi K, et al.
Bioconjugate Chemistry, 19(12), 2417-2426 (2008)
Synthesis, characterization and biocompatibility of PEGA resins.
Auzanneau FI, et al.
Journal of Peptide Science, 1(1), 31-44 (1995)
A PEGA resin for use in the solid-phase chemical?enzymatic synthesis of glycopeptides.
Meldal M, et al.
Journal of the Chemical Society. Chemical Communications, 16, 1849-1850 (1994)
Large scale modification of biomolecules using immobilized sortase A from Staphylococcus aureus
Steinhagen M, et al.
Bioorganic & Medicinal Chemistry, 21(12), 3504-3510 (2013)
Chemical ligation of unprotected peptides directly from a solid support.
Camarero JA, et al.
The Journal of Peptide Research, 51(4), 303-316 (1998)
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Related Content

Acrylamide-PEG Co-polymer (“PEGA”) Resin

The high swelling volume of PEGA resins makes the functionalities located within the polymer bead accessible to large biomolecules.

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