Secondary ADCs: For pre-screening and determination of antibody (Human IgG Fc) cytotoxicity as Amanitin bioconjugates.
Conjugate: Amanitin (Non-cleavable)
Suitable for cell-based cytotoxic assay.
Specific to the Fc region of human IgGs.
Clonality: Polyclonal
Isotype: Fab Fragment
Summary
Specifications
Antibody Isotype
Fab Fragment
Species Reactivity
Human
Conjugate
Amanitin (Non-cleavable)
Applications
Application Notes
Used in cell-based cytotoxic assay. Anti-Human IgG Fc polyclonal antibody [NC-Amanitin] (Fab Fragment) is a secondary antibody-drug conjugates for pre-screening antibodies with a human IgG Fc moiety or recombinant human IgG Fc fusion proteins to determine their cytotoxicity as Amanitin bioconjugates. When applied in combination with tumor specific monoclonal antibodies or recombinant Fc fusion proteins, it can help determine the cytotoxic potential for these antibodies or proteins against target cell lines. The mono-valence nature of Fab secondary antibody-drug conjugates may have some advantage in certain applications than the full length IgG secondary ADC.
General Notes
SecADC™ Anti-Human IgG Fc polyclonal antibody [NC-Amanitin] (Fab Fragment) can be used in cell-based cytotoxicity assays to pre-screening monoclonal antibodies as ADC candidates against tumor cells. This product is a Fab fragment of an anti-human IgG Fc specific antibody conjugated to α-amanitin with a non-cleavable linker. The antibody portion is a polyclonal antibody which is specific to the Fc region of human IgGs. Alfa-amanitin is a cytotoxic small molecule which inhibits RNA polymerases II and III by interfering with RNA and DNA translocation. The non-cleavable linker connecting amanitin to the antibody is stable in extracellular fluid, but can be cleaved by unspecified mechanisms upon entering cells.
Target
Alternative Names
Ig gamma 1 chain C region; Immunoglobin heavy constant gamma 1; Immunoglobulin G; IgG; IgG heavy chain; Immunoglobulin G heavy chain; IGHG1; IGHG2; IGHG3; IGHG4;
Product Background
Pathway
IL4-mediated signaling events;
Citations
Publication ()
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