ReadiPrep™ Protein A-Agarose Resin
Ordering information
Price | |
Catalog Number | |
Unit Size | |
Quantity |
Additional ordering information
Telephone | 1-800-990-8053 |
Fax | 1-800-609-2943 |
sales@aatbio.com | |
International | See distributors |
Bulk request | Inquire |
Custom size | Inquire |
Shipping | Standard overnight for United States, inquire for international |
Storage, safety and handling
H-phrase | H303, H313, H333 |
Hazard symbol | XN |
Intended use | Research Use Only (RUO) |
R-phrase | R20, R21, R22 |
Storage | Refrigerated (2-8 °C) |
UNSPSC | 12352200 |
Related products
Overview | SDSProtocol |
ReadiPrep™ Protein-A Agarose Resin was prepared by covalently immobilizing protein A onto high-quality crosslinked beaded agarose. These agarose beads possess physical and chemical characteristics that make them suitable for use in various batch or column-type affinity purification procedures. Our ReadiPrep™ Protein-A Agarose Resin has four high-affinity binding sites that interact with the Fc region of IgG-class antibodies from selected mammalian species. Protein A agarose has pH stability from 3 to 13.
Images
Figure 1. Protein A agarose beads have physical and chemical properties that enable them to be used in a variety of batch- or column-type affinity purification procedure. Protein A contains four high-affinity binding sites interacting with the Fc region of IgG-class antibodies from selected mammalian species.
References
View all 5 references: Citation Explorer
Purification of antibodies against N-homocysteinylated proteins by affinity chromatography on Nomega-homocysteinyl-aminohexyl-Agarose
Authors: Perla, J.; Undas, A.; Twardowski, T.; Jakubowski, H.
Journal: J Chromatogr B Analyt Technol Biomed Life Sci (2004): 257-61
Authors: Perla, J.; Undas, A.; Twardowski, T.; Jakubowski, H.
Journal: J Chromatogr B Analyt Technol Biomed Life Sci (2004): 257-61
Purification and partial characterization of cathepsin D from porcine (Sus scrofa) liver using affinity chromatography
Authors: C, undefined and uri, F.; Ward, R. J.; de Azevedo Junior, W. F.; Gomes, R. A.; Arni, R. K.
Journal: Biochem Mol Biol Int (1998): 797-803
Authors: C, undefined and uri, F.; Ward, R. J.; de Azevedo Junior, W. F.; Gomes, R. A.; Arni, R. K.
Journal: Biochem Mol Biol Int (1998): 797-803
Rapid purification of a 110-kilodalton hemolysin of Actinobacillus pleuropneumoniae by monoclonal antibody-affinity chromatography
Authors: Ma, J.; Inzana, T. J.
Journal: Am J Vet Res (1992): 59-62
Authors: Ma, J.; Inzana, T. J.
Journal: Am J Vet Res (1992): 59-62
Purification of rabbit mammary prolactin receptor by acidic elution from a prolactin affinity column
Authors: Necessary, P. C.; Humphrey, P. A.; Mahajan, P. B.; Ebner, K. E.
Journal: J Biol Chem (1984): 6942-6
Authors: Necessary, P. C.; Humphrey, P. A.; Mahajan, P. B.; Ebner, K. E.
Journal: J Biol Chem (1984): 6942-6
Purification of sciatin using affinity chromatography on concanavalin A-Agarose
Authors: Markelonis, G. J.; Oh, T. H.
Journal: J Neurochem (1981): 95-9
Authors: Markelonis, G. J.; Oh, T. H.
Journal: J Neurochem (1981): 95-9
Application notes
FAQ
How can I lyse my cells without lysing the nuclear membrane?
What is the difference between FluoroQuest Anti-fading Kit I and FluoroQuest Anti-fading Kit II?
What does an assay buffer do?
How to lyse cells?
Why is my GSH concentration greater than my Total GSH concentration? Why is my calculated GSH/TGSH ratio greater than 1?
What is the difference between FluoroQuest Anti-fading Kit I and FluoroQuest Anti-fading Kit II?
What does an assay buffer do?
How to lyse cells?
Why is my GSH concentration greater than my Total GSH concentration? Why is my calculated GSH/TGSH ratio greater than 1?