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anti-HIgG(Fc)-N-DM1 ADC (CAT#: ADC-AA-008)

This ADC product is comprised of an anti-human IgG Fc specific polyclonal antibody conjugated via a noncleavable linker to DM1. The antibody portion is a secondary antibody and the drug portion, DM1, is a cytotoxic small molecule which binds to tubulins, interrupts microtubule dynamics, and induces cell death. This product displays no obvious toxicity without a primary antibody and can be a quite efficient and economical alternative to pre-screening human monoclonal antibodies as ADC candidates.

  • ADC Target
  • ADC Antibody
  • ADC Linker
  • ADC payload drug
  • Name
  • IgG Fc
  • Overview
  • The fragment crystallizable region (Fc region) is composed of the constant region of the two heavy chains that form the IgG molecule. The Fc region of IgG bears a highly conserved N-glycosylation site. Glycosylation of the Fc fragment is essential for Fc receptor-mediated activity. Fc binds to various cell receptors and complement proteins thus mediating different physiological effects of antibodies, such as opsonization, antibody dependent cellular cytotoxicity (ADCC), degranulation of mast cells, basophils, eosinophils and other processes.
  • Overview
  • anti-human IgG Fc specific polyclonal IgG antibody
  • Species Reactivity
  • Human
  • Name
  • Noncleavable linkers
  • Description
  • Noncleavable linkers, is considered noncleavable-meaning linker cleavage, and payload release does not depend on the differential properties between the plasma and some cytoplasmic compartments. Instead, the release of the cytotoxic drug is postulated to occur after internalization of the ADC via antigen-mediated endocytosis and delivery to lysosomal compartment, where the antibody is degraded to the level of amino acids through intracellular proteolytic degradation.
  • Name
  • DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
  • Description
  • Derived from Maytansinoid,a group of cytotoxins structurally similar to rifamycin, geldanamycin, and ansatrienin. The eponymous natural cytotoxic agent maytansine is a 19-member lactam (ansa
    macrolide) structure originally isolated from the Ethiopian shrub Maytenus ovatus. Maytansinoids can bind to tubulin at or near the vinblastine-binding site, which interfere the formation of microtubules and depolymerize already formed microtubules, inducing mitotic arrest in the intoxicated cells.

For Research Use Only. NOT FOR CLINICAL USE.

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Customer Reviews FAQ
def-person
Excellent
The Anti-HIgG(Fc)-N-DM1 ADC from Creative Biolabs has exceeded our expectations. Excellent for targeting microtubule dynamics, resulting in effective cell death with no unwanted toxicity.
def-person
Excellent
Remarkably effective
This ADC's precision in delivering DM1 ensures targeted disruption of tubulins, making it a vital tool in our cytotoxic studies.
def-person
Excellent
Anti-HIgG(Fc)-N-DM1 ADC provides dependable results in our lab. The noncleavable linker ensures stable delivery of DM1, enhancing the efficacy of our monoclonal antibody screenings.
def-person
Excellent
I highly recommend Anti-HIgG(Fc)-N-DM1 ADC for advanced cancer research. Its targeted action on tubulins and subsequent induction of cell death are incredibly effective and safe.
def-person
Excellent
Anti-HIgG(Fc)-N-DM1 ADC has proven to be an indispensable asset in our lab, providing consistent and reliable results in targeted cytotoxicity without primary antibody use.

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ADC-AA-037 anti-RIgG(HL)Fab-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
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ADC-AA-018 anti-HIgG(Fab)-N-DM1 ADC Noncleavable linkers DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-AA-050 Protein G-MCC-DM1 ADC MCC (Maleimidomethyl cyclohexane-1-carboxylate) DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-W-487 Anti-CD70-MCC-DM1 ADC MCC (Maleimidomethyl cyclohexane-1-carboxylate) DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
CAT# Product Name Linker Payload
ADC-AA-049 Protein G-MMAF ADC MMAF (Monomethyl auristatin F)
ADC-AA-050 Protein G-MCC-DM1 ADC MCC (Maleimidomethyl cyclohexane-1-carboxylate) DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-AA-031 anti-MIgG(Fc)Fab-N-DM1 ADC Noncleavable linkers DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-AA-056 Anti-MIgG (clone 187.1)-VC-MMAE ADC VC (valine-citrulline) MMAE (Monomethyl auristatin E)
ADC-AA-029 anti-MIgG(Fc)Fab-C-MMAE ADC Cleavable linkers MMAE (Monomethyl auristatin E)

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