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AB193258

Protein G Agarose (High Affinity)

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(5 Publications)

Protein G Agarose (High Affinity) (ab193258) contains recombinant Protein G coupled to highly cross-linked 4% agarose beads. Suitable for antibody purification and immunoprecipitation (IP) assays.

- Binding Capacity: >30 mg Goat lgG/mL medium
- Used for monoclonal and polyclonal antibody purification
- Available in different test sizes to fit your experimental needs

Key facts

Applications

IP, Purification

applications

Form

Liquid

form

Storage buffer

Constituents: 20% Ethanol

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "IP": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p>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.</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

Very high binding capacity (>30 mg IgG/mL). Minimal leaching of ligand. Suitable for column or batch purification of IgG, immunoprecipitation & ChIP (ab193258).

Contents:

Supplied as 50% slurry in 20% Ethanol.

Features:
High binding capacity: Binding of IgG ≥ 30 mg human or rabbit IgG/mL Protein G 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).
Maximum Flow Rate**: 1800 cm/hr; minimum leaching of recombinant Protein G.
**NOTE: the highest flow that beads withstand for 1 minute, without collapsing and the pressure reaching 1 MPa.

Usage:Reusable for up to 10 times without significant loss of binding capacity.

These beads are for use in column purification. If used in batch purification, we recommend not exceeding 150 x g when centrifuging.

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 6513 Hi-Bind™ Protein G-Agarose. 6513-5 is the same size as the 5 ml size of ab193258.

Protein G Agarose (High Affinity) beads are specially prepared for high IgG binding by covalently coupling recombinant Protein G to 6% cross-linked agarose beads, the most popular resin for protein affinity purification methods. Protein G is a genetically engineered protein containing three IgG-binding regions of native Protein G. The cell wall binding region, albumin binding region and other non-specific regions have been eliminated from the recombinant Protein G 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 G than standard Protein G agarose beads. The IgG binding capacity of Protein G Agarose (High Affinity) is ≥ 30 mg of human or rabbit IgG per mL of wet beads. The Protein G Agarose (High Affinity) beads display high chemical and physical stability, as well as high flow rate, hydrophilicity and high gel strength.

Properties and storage information

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

Product protocols

Target data

Publications (5)

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

The Journal of cell biology 222: PubMed36355348

2022

REC drives recombination to repair double-strand breaks in animal mtDNA.

Applications

Unspecified application

Species

Unspecified reactive species

Anna Klucnika,Peiqiang Mu,Jan Jezek,Matthew McCormack,Ying Di,Charles R Bradshaw,Hansong Ma

Nature communications 13:6548 PubMed36319643

2022

FOXQ1 recruits the MLL complex to activate transcription of EMT and promote breast cancer metastasis.

Applications

Unspecified application

Species

Unspecified reactive species

Allison V Mitchell,Ling Wu,C James Block,Mu Zhang,Justin Hackett,Douglas B Craig,Wei Chen,Yongzhong Zhao,Bin Zhang,Yongjun Dang,Xiaohong Zhang,Shengping Zhang,Chuangui Wang,Heather Gibson,Lori A Pile,Benjamin Kidder,Larry Matherly,Zhe Yang,Yali Dou,Guojun Wu

Oncology letters 24:253 PubMed35765282

2022

miR-4735-3p inhibits cell migration and invasion of gastric cancer by downregulating NEDD9.

Applications

Unspecified application

Species

Unspecified reactive species

Yanchun Ma

Cell transplantation 29:963689720929983 PubMed32686982

2020

LncRNA DLX6-AS1 Contributes to Epithelial-Mesenchymal Transition and Cisplatin Resistance in Triple-negative Breast Cancer via Modulating Mir-199b-5p/Paxillin Axis.

Applications

Unspecified application

Species

Unspecified reactive species

Chuang Du,Yan Wang,Yingying Zhang,Jianhua Zhang,Linfeng Zhang,Jingruo Li

Cell biochemistry and function 37:545-552 PubMed31429100

2019

Sodium nitroprusside induces H-Ras depalmitoylation and alters the cellular response to hypoxia in differentiated and undifferentiated PC12 cells.

Applications

Unspecified application

Species

Unspecified reactive species

Galina Goloshvili,Tamar Barbakadze,David Mikeladze
View all publications

Product promise

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