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PureProteome Protein G Magnetic Bead System

The PureProteome Protein G Magnetic Bead System is a powerful system that helps researchers purify proteins by maximizing recovery and eliminating variability

Synonym(s):

Protein G Magnetic Beads, PureProteome Magnetic Beads

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Pack SizeSKUAvailabilityPrice
2 x 1 mL
Please contact Customer Service for Availability
₪1,658.00
10 mL
Please contact Customer Service for Availability
₪7,733.00

About This Item

UNSPSC Code:
41105507
NACRES:
NA.56
eCl@ss:
32160405

₪1,658.00


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packaging

pkg of 2 × 1 mL

manufacturer/tradename

PureProteome

technique(s)

depletion: suitable (serum), immunoprecipitation (IP): suitable, protein purification: suitable

particle size

10 μm

capacity

2.5-3.5 μg/μL, suspension binding capacity (rabbit IgG)

shipped in

wet ice

General description

The PureProteome Protein G Magnetic Beads contain Protein G, a binding protein for antibodies, which is coated on the surface of the beads. These beads are designed to isolate immunoglobulins (IgG) from complex mixtures through antibody-affinity purification. These beads are used in conjunction with a magnetic stand to immobilize the beads. Following this step, the sample is washed to remove any impurities, and then the immobilized IgG can be eluted for further analysis or experimentation.

Application

PureProteome Protein G Magnetic Bead System is suitable for:
  • serum depletion
  • immunoprecipitation
  • protein purification    

PureProteome Protein G Magnetic Bead System is suitable:

  • for isolation of the immunoglobulin G (IgG) fraction from a small volume of plasma
  • for co-immunoprecipitation (Co-IP)

Features and Benefits

  • PureProteome Magnetic Beads are very well suited for fully automated purification process using the KingFisher Duo particle processor, it is not dependent on the cell lysate clarification step
  • The entire process is reproducible, and the results are comparable to that of a standard protocol using the PureProteome Magnetic Stand
  • PureProteome Magnetic Beads is compatible with any automated system for low, medium, or high-throughput sample preparation.

Legal Information

PureProteome is a trademark of Merck KGaA, Darmstadt, Germany

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This Item
LSKMAGALSKMAGHLSKMAGL10
manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

manufacturer/tradename

PureProteome

particle size

10 μm

particle size

10 μm

particle size

10 μm

particle size

10 μm

packaging

pkg of 2 × 1 mL

packaging

pkg of 2 × 1 mL

packaging

pkg of 10 mL

packaging

pkg of 10 mL

capacity

2.5-3.5 μg/μL, suspension binding capacity (rabbit IgG)

capacity

1.5-2.5 μg/μL, suspension binding capacity (rabbit IgG)

capacity

1-5.5 mg/mL, bead suspension binding capacity (protein)

capacity

-

technique(s)

depletion: suitable (serum), protein purification: suitable, immunoprecipitation (IP): suitable

technique(s)

depletion: suitable (serum), immunoprecipitation (IP): suitable, protein purification: suitable

technique(s)

protein purification: suitable (histidine tagged recombinant protein)

technique(s)

depletion: suitable (serum), protein purification: suitable

shipped in

wet ice

shipped in

wet ice

shipped in

ambient

shipped in

wet ice


Storage Class

12 - Non Combustible Liquids

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Sens. 1

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Related Content

Traditionally, protein purification from E. coli consists of four distinct phases: harvest, bacterial cell lysis, lysate clarification and protein purification. Bacterial lysis typically requires several time-consuming, hands-on steps, such as freeze/thaw cycles and sonication. These harsh lysis techniques may negatively impact protein quality and contribute to sample-to-sample variability. To maintain protein activity and integrity, detergent-based lysis buffers are routinely used to avoid mechanical protein extraction methods. Regardless of the lysis method used, centrifugation is traditionally required to pellet unwanted cell debris and permit recovery of the clarified lysate. The final step, purification, is frequently performed using affinity media specific for expressed epitope tags. Agarose-based media have typically been used, either as a slurry in microcentrifuge tubes or packed into gravity-driven or spin columns. While easier to manipulate, columns are greatly affected by lysate consistency and carryover of cell debris, which can lead to clogging of the column frits.

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Global Trade Item Number

SKUGTIN
LSKMAGG1004053252323188
LSKMAGG0204053252373053

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