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Journal ArticleDOI

Selection of large diversities of antiidiotypic antibody fragments by phage display.

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TLDR
In this article, the authors describe a fast and reliable technique for generating large diversities of anti-iotypic single chain antibody fragments from non-immunized phagemid libraries using phage display.
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This article is published in Journal of Molecular Biology.The article was published on 2002-02-01. It has received 140 citations till now. The article focuses on the topics: Phage display & Phagemid.

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Citations
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Journal ArticleDOI

Active targeting schemes for nanoparticle systems in cancer therapeutics.

TL;DR: The targeting schemes explored for many of the reported nanoparticle systems suggest the great potential of targeted delivery to revolutionize cancer treatment.
Journal ArticleDOI

Nanoparticle Probes for the Detection of Cancer Biomarkers, Cells, and Tissues by Fluorescence

TL;DR: Overcoming Limitations in Nanoparticle Drug Delivery: Triggered, Intravascular Release to Improve Drug Penetration into Tumors and Design Considerations for Tumour-Targeted Nanoparticles.
Journal ArticleDOI

Applications of single-chain variable fragment antibodies in therapeutics and diagnostics.

TL;DR: This review will show the tremendous versatility and importance of scFv fragments as they provide the basic antigen binding unit for a multitude of engineered Abs for use as human therapeutics and diagnostics.
References
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Journal ArticleDOI

Filamentous fusion phage: novel expression vectors that display cloned antigens on the virion surface

TL;DR: Foreign DNA fragments can be inserted into filamentous phage gene III to create a fusion protein with the foreign sequence in the middle that is incorporated into the virion, which retains infectivity and displays the foreign amino acids in immunologically accessible form.
Journal ArticleDOI

Phage antibodies: filamentous phage displaying antibody variable domains

TL;DR: It is shown that complete antibody V domains can be displayed on the surface of fd bacteriophage, that the phage bind specifically to antigen and that rare phage can be isolated after affinity chromatography.
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By-passing immunization: Human antibodies from V-gene libraries displayed on phage

TL;DR: The results suggest that a single large phage display library can be used to isolate human antibodies against any antigen, by-passing both hybridoma technology and immunization.
Journal ArticleDOI

Making Antibodies by Phage Display Technology

TL;DR: Human antibody fragments with many different binding specificities have been isolated from the same phage repertoire, including haptens, carbohydrates, secreted and cell surface proteins, viral coat proteins, and intracellular antigens from the lumen of the endoplasmic reticulum and the nucleus.
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