Phage Display-Selected Sequences of the Heavy-Chain CDR3 Loop of the Anti-Digoxin Antibody 26-10 Define a High Affinity Binding Site for Position 16-Substituted Analogs of Digoxin

Journal of Biological Chemistry - United States
doi 10.1074/jbc.m008108200
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Society for Biochemistry & Molecular Biology (ASBMB)

Related search

Affinity Labelling of the Binding Site of Rabbit Antibody. Evidence for the Involvement of the Hypervariable Regions of the Heavy Chain

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
1974English

Correction: Treatment of Digoxin Overdose With Antigen-Binding Fragments of Digoxin-Specific Antibodies

BMJ
1982English

The Electrophysiologic Effects of Low and High Digoxin Concentrations on Isolated Mammalian Cardiac Tissue: Reversal by Digoxin-Specific Antibody

Journal of Clinical Investigation
Medicine
1972English

Development of Radioimmunoassay for Measurement of Serum Digoxin in Digitalized Patients Using Novel Anti-Digoxin Antiserum

Biological and Pharmaceutical Bulletin
MedicinePharmacologyPharmaceutical Science
2002English

Effects of Digoxin-Specific Antibodies on Accumulation and Binding of Digoxin by Human Erythrocytes

Journal of Clinical Investigation
Medicine
1973English

The Bioavailability of Digoxin

The Lancet
Medicine
1972English

A ``Loop Entropy Reduction'' Phage-Display Selection for Folded Amino Acid Sequences

Protein Science
BiochemistryMedicineMolecular Biology
2001English

Selection of Single Chain Antibody Fragments Binding to the Extracellular Domain of 4-1bb Receptor by Phage Display Technology

Tumor Biology
MedicineCancer Research
2017English

A Large Human Domain Antibody Library Combining Heavy and Light Chain CDR3 Diversity

Molecular Immunology
ImmunologyMolecular Biology
2010English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy