|Related Categories||Affinity Chromatography, Affinity Resins, Antibodies, Antibody Purification and Characterization, Core Bioreagents,|
|form||aqueous ethanol suspension|
|extent of labeling||~6 mg per mL|
|matrix||Sepharose 4B Fast Flow|
|matrix activation||cyanogen bromide|
|matrix spacer||1 atom|
|capacity||≥30 mg/mL binding capacity (human IgG)|
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1, 5 mL in glass bottle
Suspension in 20% ethanol
Protein A-Sepharose is used for affinity chromatography, antibody purification and characterization, immunoaffinity matrices, protein chromatography, protein A, G and L resins, and recombinant protein expression and analysis. Protein A-Sepharose® has been used to develop strategies for investigating protein interactions, to improve the detection of celiac disease, and to study diabetes in children.
Sepharose is a registered trademark of GE Healthcare
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Keywords: Buffers, Cell biology, Epigenetics, Immunohistochemistry, Immunoprecipitation, Molecular biology, Neuroscience, Western blot
Rat seminiferous epithelium contains a unique junction (Ectoplasmic specialization) with signaling properties both of cell/cell and cell/matrix junctions. Dedhar, S., et al. Biol. Reprod. 64, 396-407, (2001)
The Autocatalytic Release of a Putative RNA Virus Transcription Factor from Its Polyprotein Precursor Involves Two Paralogous Papain-like Proteases That Cleave the Same Peptide Bond. Ziebuhr, J., et al. J. Biol. Chem. 276, 33220-33232, (2001)
Analysis Of Mutually Exclusive Alternatively Spliced Serpin-1 Isoforms And Identification Of Serpin-1 Proteinase Complexes In Manduca Sexta Hemolymph. Ragan, E.J., et al. J. Thorac. Cardiovasc. Surg. 285, 29642-50, (2010)
Identification of proteins interacting with lactate dehydrogenase in claw muscle of the porcelain crab Petrolisthes cinctipes. Cayenne, A.P., et al. Comp. Biochem. Physiol. 6, 393-398, (2011)
T-cell synapse formation depends on antigen recognition but not CD3 interaction: studies with TCR:ζ, a candidate transgene for TCR gene therapy. Roszik, J., et al. Eur. J. Immunol. 41, 1288-1297, (2011)
Improved efficacy by using the pTnT-rhtTG plasmid for the detection of celiac disease specific tissue transglutaminase autoantibodies in radioligand binding assays Kjellerås, J., et al. Scand. J. Clin. Lab. Invest. 71, 701-704, (2011)
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