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ERBB2 & CD3

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Anti-ERBB2 & CD3 Products

    • Target: HER2
    • Drug: Gly5-modified DM1 (Gly5-modified N2'-Deacetyl-N2'-(3-mercapto-1-oxopropyl)maytansine)
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    • Target: HER2
    • Linker: VC-PAB (valine-citrulline-p-aminobenzoyloxycarbonyl)
    • Drug: MMAE (Monomethyl auristatin E)
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    • Target: Her2
    • Linker: valine-citruline-p-amino-benzoyl-carbonate (VCP)-cyclooctyne
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: BMPEO (bis-maleimido-trioxyethylene glycol)
    • Drug: DM1 (N2'-Deacetyl-N2'-(3-mercapto-1-oxopropyl)maytansine)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: NGMs(next generation maleimides)
    • Drug: MMAE (monomethyl auristatin E)
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    • Target: HER2
    • Linker: SMCC (N-succinimidyl-4-(N-maleimidomethyl)-cyclohexane-1-carboxylate)
    • Drug: DM1(N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)-maytansine)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DBCO (Dibenzocyclooctyl)
    • Drug: MMAF (Monomethyl auristatin F)
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    • Target: HER2
    • Linker: mc(maleimidocaproyl)
    • Drug: MMAF(monomethyl auristatin F)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DUBA (DUocarmycinhydroxyBenzamide-Azaindole
      linker) ("mc"-VC-PABC-CM)
    • Drug: Duocarmycins
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: VC (valine-citrulline)
    • Drug: MMAE(monomethyl auristatin E)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: DBM(dibromomaleimide)
    • Drug: MMAF(monomethyl auristatin F)
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    • Target: HER2
    • Linker: MP(T-VC)
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino) phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: MC-VC-PABC (maleimidocaproyl-valine-citrulline-p-aminobenzoyloxycarbonyl)
    • Drug: (S,E)-N-(4-(aminomethyl)benzylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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  • Anti-HER2-DOX ADC (ADC-131LZY)
    • Target: HER2
    • Linker: thiomaleamicacids-p-aminobenzyloxycarbonyl
    • Drug: doxorubicin
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    • Target: HER2
    • Linker: mcc (Maleimidomethyl cyclohexane-1-carboxylate)
    • Drug: DM1 (N2'-Deacetyl-N2'-(3-mercapto-1-oxopropyl)maytansine)
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    • Target: HER2
    • Linker: MT-VC
    • Drug: (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)-N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide
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    • Target: HER2
    • Linker: SPP (N-succinimidyl-4-(2-pyridyldithio)pentanoate)
    • Drug: DM1(N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)-maytansine)
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    • Target: HER2
    • Linker: [14C]-SMCC
    • Drug: DM1(N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)-maytansine)
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    • Target: Her2
    • Linker: MCC (Maleimidomethyl cyclohexane-1-carboxylate)
    • Drug: DM1(N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)-maytansine)
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    • Target: Her2
    • Linker: mc-VC-PABC (maleimidocaproyl valine-citrulline-p-aminobenzyl carbamoyl)
    • Drug: MMAE (monomethyl auristatin E)
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    • Target: HER2
    • Linker: SPDP ( N-succinimidyl 3-(2-pyridyldithio)propionate)
    • Drug: DM1 (N2'-Deacetyl-N2'-(3-mercapto-1-oxopropyl)maytansine)
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    • Target: HER2
    • Linker: SPP (N-succinimidyl-4-(2-pyridyldithio)pentanoate)
    • Drug: DM1 (N2'-Deacetyl-N2'-(3-mercapto-1-oxopropyl)maytansine)
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    • Target: HER2
    • Linker: The linker contains two ethylene glycol moieties modified with a terminal alkoxy-amine group to improve solubility and minimize export of the more hydrophilic derivatized analogs by drug pumps
    • Drug: auristatin
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    • Target: Her2
    • Linker: VC(valine-citrulline)
    • Drug: [14C]MMAE(14C-labeled monomethyl auristatin E)
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For Research Use Only. Not For Clinical Use.


Background

This gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways, such as those involving mitogen-activated protein kinase and phosphatidylinositol-3 kinase. Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported, with the most common allele, Ile654/Ile655, shown here. Amplification and/or overexpression of this gene has been reported in numerous cancers, including breast and ovarian tumors.
ERBB2 & CD3
The protein encoded by this gene is part of the T-cell receptor/CD3 complex (TCR/CD3 complex) and is involved in T-cell development and signal transduction. The encoded membrane protein represents the delta subunit of the CD3 complex, and along with four other CD3 subunits, binds either TCR alpha/beta or TCR gamma/delta to form the TCR/CD3 complex on the surface of T-cells. Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK). Two transcript variants encoding different isoforms have been found for this gene. Other variants may also exist, but the full-length natures of their transcripts has yet to be defined.
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