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Antibody Fragment Production (CAT#: STEM-MB-0134-WXH)

Introduction

Antibodies are powerful tools for the detection and purification of proteins and molecules. Although whole antibodies (typically IgG or IgM) are suitable for most immunoassay applications, the performance of certain steps is enhanced by the use of antibody fragments such as Fab.
There are three main types of antibody fragments: antigen-binding fragment (Fab), single-chain variable fragment (scFv), and single-domain antibody (sdAb). All of these antibody fragments are smaller in size than whole antibodies. This allows them to bind to the cryptic epitope of the whole antibody. Smaller antibody sizes help reduce scatter, resulting in higher resolution images.
In terms of therapeutic applications, small molecular weight also means efficient penetration and rapid clearance. In addition, small-molecule antibodies can be expressed in large quantities in prokaryotic systems, ultimately producing proteins in sufficient quantities for diagnostics, therapeutics, and structural studies.




Applications

• Access to tissues inaccessible to intact antibodies for therapeutic effects and immunohistochemical staining.
• Significantly reduce the non-specific binding of Fc.
• The binding of antibody to proteinA and proteinG can be reduced in precipitation and western blotting.
• Better tissue permeability, better staining effect in immunohistochemical experiments.
• Avoid the steric hindrance effect of full-length antibodies, and have higher sensitivity in solid-phase antigen detection.
• In the study of antigen-antibody binding, the interference of Fc-related factors can be avoided.
• Simplified systems for studying the structural basis of immune recognition by X-ray crystallography or NMR.
• Compared with full-length antibodies, it has lower immunogenicity in vivo experiments.
• Can be coupled or combined with enzymes, toxins, drugs and radionuclides, etc.

Procedure

Method 1: Enzymatic hydrolysis - usually using papain or pepsin to degrade human immunoglobulin G
Method 2: Gene Recombination - Using Gene Recombination Technology

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