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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.
Related Products
- anti-Rat IgG(Fc)Fab-N-MMAF ADC (CAT#: ADC-AA-041)
- anti-RIgG(HL)-C-MMAF ADC (CAT#: ADC-AA-035)
- anti-MIgG(Fc)Fab-C-DMDM ADC (CAT#: ADC-AA-030)
- anti-Rat IgG(Fc)-N-MMAF ADC (CAT#: ADC-AA-039)
- anti-RIgG(HL)-N-MMAF ADC (CAT#: ADC-AA-034)
- anti-MIgG(Fc)-C-DMDM ADC (CAT#: ADC-AA-024)
- anti-HIgG(Fc)Fab-N-AAMT ADC (CAT#: ADC-AA-016)
- anti-Rat IgG(HL)Fab-N-MMAF ADC (CAT#: ADC-AA-046)
- anti-HIgG(Fc)-C-PNU ADC (CAT#: ADC-AA-007)
- anti-HIgG(Fc)-C-MMAF ADC (CAT#: ADC-AA-002)
Published Data
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Customer Reviews and FAQs
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Customer Reviews
FAQ
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.
Excellent
Remarkably effective This ADC's precision in delivering DM1 ensures targeted disruption of tubulins, making it a vital tool in our cytotoxic studies.
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.
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.
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.
Quick Links
Other Products
Same Linker
Same Payload
Same Target
CAT# | Product Name | Linker | Payload |
ADC-AA-045 | anti-Rat IgG(HL)-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-009 | anti-HIgG(Fc)Fab-N-MMAF ADC | Noncleavable linkers | MMAF (Monomethyl auristatin F) |
ADC-AA-037 | anti-RIgG(HL)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 |
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-W-572 | Anti-ERBB2 (Trastuzumab-Fab)-SPP-DM1 ADC | SPP (N-succinimidyl-4-(2-pyridyldithio)pentanoate) | DM1 (N2’-Deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine) |
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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