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anti-HIgG(Fc)Fab-N-DM1 ADC (CAT#: ADC-AA-015)

This ADC product is comprised of a Fab fragment of an anti-human IgG Fc specific polyclonal antibody conjugated via a noncleavable linker to DM1. The antibody portion is a Fab fragment of 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
  • Fab fragment of anti-human IgG Fc specific polyclonal 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
Creative Biolabs' anti-HIgG(Fc)Fab-N-DM1 ADC has dramatically improved our screening process. The noncleavable linker and DM1's tubulin-binding efficacy make it a reliable tool for targeting cell structures without unwanted toxicity.
def-person
Excellent
Using the anti-HIgG(Fc)Fab-N-DM1 ADC, we've seen precise targeting and effective induction of cell death in our studies. Its stability and consistent performance are impressive.
def-person
Excellent
The noncleavable linker in this ADC ensures that DM1 remains bound and effective, which is crucial for our studies involving microtubule dynamics. It's been an essential part of our research toolkit.
def-person
Excellent
I highly recommend the anti-HIgG(Fc)Fab-N-DM1 ADC for its efficacy and safety. It provides a cost-effective method for pre-screening ADC candidates, significantly cutting down our lab's expenses.
def-person
Excellent
This ADC product from Creative Biolabs has been a game changer in our ADC development, providing targeted cytotoxicity with minimal off-target effects. It's particularly useful for labs focused on enhancing precision in drug delivery.
def-person
Excellent
The anti-HIgG(Fc)Fab-N-DM1 ADC is a standout in our lab for its robust performance in inducing targeted cell death without systemic toxicity. It has streamlined our workflow and improved our screening outcomes.

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ADC-AA-029 anti-MIgG(Fc)Fab-C-MMAE ADC Cleavable linkers MMAE (Monomethyl auristatin E)
ADC-AA-031 anti-MIgG(Fc)Fab-N-DM1 ADC Noncleavable linkers DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-AA-027 anti-MIgG(Fc)Fab-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
ADC-AA-048 Protein G-VC-MMAE ADC VC (valine-citrulline) MMAE (Monomethyl auristatin E)
ADC-AA-028 anti-MIgG(Fc)Fab-C-MMAF ADC Cleavable linkers MMAF (Monomethyl auristatin F)
CAT# Product Name Linker Payload
ADC-AA-063 Anti-HIgG(Fab)-N-MMAF ADC Noncleavable linkers MMAF
ADC-AA-037 anti-RIgG(HL)Fab-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
ADC-AA-046 anti-Rat IgG(HL)Fab-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
ADC-AA-027 anti-MIgG(Fc)Fab-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
ADC-AA-039 anti-Rat IgG(Fc)-N-MMAF ADC Noncleavable linkers MMAF (Monomethyl auristatin F)
CAT# Product Name Linker Payload
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ADC-W-495 Anti-EGFR (J2898A)-SMCC-DM1 ADC SMCC (N-succinimidyl 4-(Nmaleimidomethyl)cyclohexane-1-carboxylate) DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-AA-054 Protein A-MCC-DM1 ADC MCC (Maleimidomethyl cyclohexane-1-carboxylate) DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine)
ADC-W-541 Anti-CD44 (clone BIWA 4)-DM1 ADC 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)

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