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P3476

Millipore

Protein A–Agarose Fast Flow

50%, aqueous suspension

Synonym(s):

Protein A resin

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About This Item

MDL number:
UNSPSC Code:
41106500
NACRES:
NA.56
Pricing and availability is not currently available.

biological source

protein A from Staphylococcus aureus

description

protein A leaching <= 5 ng/mL

form

aqueous suspension

concentration

50%

matrix

6% Fast-flow beaded agarose

capacity

37-43 mg/mL binding capacity (IgG)

storage temp.

2-8°C

Application

Protein A-agarose is used for affinity chromatography, antibody purification, characterization, and protein A, G, and L resins. Protein A-agarose has been used to study the effects of protein A immunoadsorption in patients with chronic dilated cardiomyopathy as well as to study multiple sclerosis and gastric cancer.
Protein A–Agarose Fast Flow has been used:

  • in the immunoprecipitation of protein complex TRRAP/p400 from viral transfected human normal kidney and baby rat kidney cells[1]
  • in the purification of polyclonal IgG from antisera[2]
  • in the immunoprecipitation assay of human embryonic kidney cells transfected by HA-Ano9 plasmids[3]

Features and Benefits

  • High capacity
  • Low leakage
  • Stable affinity medium for the purification of monoclonal and polyclonal antibodies
  • Ideal for rapid capture of immunoglobulins from cell culture

Physical form

Suspension containing 0.01% thimerosal

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Nolan J Hoffman et al.
Molecular metabolism, 41, 101048-101048 (2020-07-02)
Glycogen is a major energy reserve in liver and skeletal muscle. The master metabolic regulator AMP-activated protein kinase (AMPK) associates with glycogen via its regulatory β subunit carbohydrate-binding module (CBM). However, the physiological role of AMPK-glycogen binding in energy homeostasis
Spiro Marangoudakis et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 32(30), 10365-10369 (2012-07-28)
Ca(V)2.2 (N-type) calcium channels control the entry of calcium into neurons to regulate essential functions but most notably presynaptic transmitter release. Ca(V)2.2 channel expression levels are precisely controlled, but we know little of the cellular mechanisms involved. The ubiquitin proteasome
Lu Chen et al.
STAR protocols, 2(2), 100477-100477 (2021-05-18)
The majority of the mammalian genome is transcribed into non-coding RNAs, many of which co-evolve with RNA-binding proteins (RBPs) to function as biochemically defined and tractable ribonucleoproteins (RNPs). Here, we applied icSHAPE- a robust and versatile RNA structural probing pipeline-
Henrik Buschmann et al.
Journal of cell science, 128(11), 2033-2046 (2015-04-25)
The preprophase band of microtubules performs the crucial function of marking the plane of cell division. Although the preprophase band depolymerises at the onset of mitosis, the division plane is 'memorized' by a cortical division zone to which the phragmoplast
Boris Gorbatyuk et al.
Molecular microbiology, 55(4), 1233-1245 (2005-02-03)
DnaA protein binds bacterial replication origins and it initiates chromosome replication. The Caulobacter crescentus DnaA also initiates chromosome replication and the C. crescentus response regulator CtrA represses chromosome replication. CtrA proteolysis by ClpXP helps restrict chromosome replication to the dividing

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Workflows for monoclonal antibody adalimumab characterization ensure drug safety and efficacy through critical quality attribute analysis.

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Workflows for monoclonal antibody adalimumab characterization ensure drug safety and efficacy through critical quality attribute analysis.

Protocols

SEC-MS protocol for rapid glycoprofiling of monoclonal antibodies with antibody purification and mass spectrometer calibration.

SEC-MS protocol for rapid glycoprofiling of monoclonal antibodies with antibody purification and mass spectrometer calibration.

SEC-MS protocol for rapid glycoprofiling of monoclonal antibodies with antibody purification and mass spectrometer calibration.

SEC-MS protocol for rapid glycoprofiling of monoclonal antibodies with antibody purification and mass spectrometer calibration.

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