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AB193254

Protein A Agarose

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(10 Publications)

Protein A Agarose (ab193254) is part of the reagents, controls & accessories range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.

Key facts

Applications

IP, Purification

applications

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "IP": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "Purification": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p>Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants.</p>" } } }

Product details

High binding capacity (>20 mg IgG/mL). Minimal leaching of ligand. Suitable for column or batch purification of IgG, immunoprecipitation & ChIP (ab193254).

Contents:

Supplied as a 50% slurry in 20% Ethanol.

Features:

High binding capacity = Binding of IgG ≥ 20 mg human or rabbit IgG/mL Protein A Agarose.
Minimal leaching of the ligand
Flow Rate Tested* = 2.89 mL/min.
*Test condition: = Calculations based on the time required to pass 18 mL of water through 2 mL settled beads (column diameter 1.5 cm).
Usage = Reusable for up to 10 times without significant loss of binding capacity.

Store beads at 4°C.

The beads may be damaged above 40°C.

DO NOT FREEZE.

Wash beads 3 times with 3x bead volume of desired buffer before use.

Applications:
- Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants.
- Isolation of antibody/antigen complexes in immunoprecipitation experiments, since only the Fc region is involved in antibody binding and the Fab region is available for binding antigen.

This product is manufactured by BioVision, an Abcam company and was previously called 6526 Protein A-Agarose. 6526-100 is the same size as the 100 ml size of ab193254.

Protein A Agarose beads are prepared by covalently coupling recombinant Protein A to 6% cross-linked Agarose beads, the most popular resin for protein affinity purification methods. Protein A is a genetically engineered protein containing five IgG-binding regions of native Protein A. The cell wall binding region, albumin binding region and other non-specific regions have been eliminated from the recombinant Protein A to ensure maximum specific IgG binding. The coupling technique is optimized to give a higher binding capacity for IgG and minimum leaching of recombinant Protein A compared to standard Protein A agarose beads. The IgG binding capacity of Protein A Agarose is ≥ 20 mg human or rabbit IgG per mL of wet beads. Protein A Agarose beads display high chemical and physical stability as well as high flow rate, hydrophilicity and high gel strength. This product can be used for IgG purification and immunoprecipitation.

Properties and storage information

Shipped at conditions
Blue Ice
Appropriate long-term storage conditions
+4°C

Product protocols

Target data

Publications (10)

Recent publications for all applications. Explore the full list and refine your search

International journal of molecular medicine 50: PubMed35775376

2022

Lamin B2 contributes to the proliferation of bladder cancer cells via activating the expression of cell division cycle‑associated protein 3.

Applications

Unspecified application

Species

Unspecified reactive species

Junpeng Ji,Huibing Li,Jing Chen,Wenjun Wang

Journal of neurochemistry 162:156-165 PubMed35526109

2022

Raf kinase inhibitory protein reduces bradykinin receptor desensitization.

Applications

Unspecified application

Species

Unspecified reactive species

Samuel B Chivers,Allison Doyle Brackley,Nathaniel A Jeske

Chinese medical journal 134:2340-2352 PubMed34561318

2021

Two naturally derived small molecules disrupt the sineoculis homeobox homolog 1-eyes absent homolog 1 (SIX1-EYA1) interaction to inhibit colorectal cancer cell growth.

Applications

Unspecified application

Species

Unspecified reactive species

Jing Wu,Bin Huang,Hong-Bo He,Wen-Zhu Lu,Wei-Guo Wang,Hong Liu

Science (New York, N.Y.) 373: PubMed34437091

2021

Enterically derived high-density lipoprotein restrains liver injury through the portal vein.

Applications

Unspecified application

Species

Unspecified reactive species

Yong-Hyun Han,Emily J Onufer,Li-Hao Huang,Robert W Sprung,W Sean Davidson,Rafael S Czepielewski,Mary Wohltmann,Mary G Sorci-Thomas,Brad W Warner,Gwendalyn J Randolph

Breast cancer research : BCR 22:125 PubMed33187540

2020

CRIPTO antagonist ALK4-Fc inhibits breast cancer cell plasticity and adaptation to stress.

Applications

Unspecified application

Species

Unspecified reactive species

Ozlen Balcioglu,Richard E Heinz,David W Freeman,Brooke L Gates,Berhane M Hagos,Evan Booker,Elnaz Mirzaei Mehrabad,Hyrum T Diesen,Kishan Bhakta,Supraja Ranganathan,Masami Kachi,Mathias Leblanc,Peter C Gray,Benjamin T Spike

American journal of translational research 12:5064-5079 PubMed33042406

2020

Intramuscular accumulation of pentadecanoic acid activates AKT1 to phosphorylate NCOR1 and triggers FOXM1-mediated apoptosis in the pathogenesis of sarcopenia.

Applications

Unspecified application

Species

Unspecified reactive species

Fa-Xiu Chen,Ning Du,Jian Hu,Fang Ning,Xun Mei,Qiang Li,Le Peng

International journal of biological sciences 16:1059-1070 PubMed32140073

2020

Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4 E3 ligases to inhibit colorectal cancer cell growth.

Applications

Unspecified application

Species

Unspecified reactive species

Chunmei Yang,Jing Wu,Hongbo He,Hong Liu

Antioxidants (Basel, Switzerland) 8: PubMed31480513

2019

SIRT1-Dependent Upregulation of Antiglycative Defense in HUVECs Is Essential for Resveratrol Protection against High Glucose Stress.

Applications

Unspecified application

Species

Unspecified reactive species

Silvano Jr Santini,Valeria Cordone,Mahmut Mijit,Virginio Bignotti,Pierpaolo Aimola,Vincenza Dolo,Stefano Falone,Fernanda Amicarelli

The Journal of biological chemistry 294:10969-10986 PubMed31152063

2019

Musashi interaction with poly(A)-binding protein is required for activation of target mRNA translation.

Applications

Unspecified application

Species

Unspecified reactive species

Chad E Cragle,Melanie C MacNicol,Stephanie D Byrum,Linda L Hardy,Samuel G Mackintosh,William A Richardson,Nicola K Gray,Gwen V Childs,Alan J Tackett,Angus M MacNicol

The Journal of biological chemistry 292:10651-10663 PubMed28490631

2017

A split-luciferase complementation, real-time reporting assay enables monitoring of the disease-associated transmembrane protein TREM2 in live cells.

Applications

Unspecified application

Species

Unspecified reactive species

Megan M Varnum,Kevin A Clayton,Asuka Yoshii-Kitahara,Grant Yonemoto,Lacin Koro,Seiko Ikezu,Tsuneya Ikezu
View all publications

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