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Merck
CN

LSKMAGS15

PureProteome Magnetic Stand, 15 mL

The PureProteome Magnetic Stand, 15 mL is designed for use with PureProteome Magnetic Beads in affinity purifications (e. g., His-tag purifications or immunoprecipitations).

Synonym(s):

Magnetic Stand for 15 mL Tubes, Magnetic Stand for PureProteome Magnetic Beads

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About This Item

UNSPSC Code:
41116133
NACRES:
NA.56
eCl@ss:
32011202
Manufacturer/tradename:
PureProteome
Feature:
binder
Material:
self-standing
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material

self-standing

feature

binder

manufacturer/tradename

PureProteome

technique(s)

RNA purification: suitable (with magnetic beads), protein purification: suitable

shipped in

ambient

General description

PureProteome Magnetic Stand significantly enhance the capture efficiency of PureProteome beads, which possess a high binding capacity.

Application

PureProteome Magnetic Stand, 15 mL I suitable for:
  • purification with magnetic beads
  • protein purification
  • in the purification of the heat shock protein 90 (Hsp90)/ Cdc37 (cell division cycle 37)/ Cyclin-dependent kinase 4 (Cdk4) complex to incubate and wash the beads with 10 bed volumes of lysis buffer

Other Notes

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.




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

Read an automated protocol for protein purification using PureProteome™ nickel magnetic beads on the AAW™ automated assay workstation and see results comparing manual vs automated runs.

Purification of recombinant proteins expressed in E.coli requires many time-consuming steps. To liberate the protein of interest, traditional bacterial lysis relies on the addition of lysozyme and a combination of sonication and repeated freeze/thaw cycles to break the bacterial cell wall. Disruption of the cell is accompanied by an increase in the viscosity of the suspension, due to the release of DNA. An endonuclease is added to digest the DNA, thus reducing the viscosity of the lysate. Finally, to render the lysate compatible with traditional purification methods, insoluble cell debris must be removed by centrifugation.

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Global Trade Item Number

SKUGTIN
LSKMAGS1504053252411717