Breast cancer subtyping (Luminal, HER2+, triple-negative, etc.) shapes endocrine, anti-HER2, and chemo/IO strategies. Recurrent nodes include ER/PR, ERBB2, Ki-67, BRCA1/2, PIK3CA/PTEN, and CDK4/6. We provide subtype biomarker antibodies and probes (CDK4/6, PARP, PI3Kα, mTOR) for resistance clones, signaling feedback, and combination studies.
Focus areas: CDK4/6–endocrine resistance, HER2-low & ADCs, TNBC immune milieu, BRCA/HRD & PARP
Commonly used for mechanistic studies; follow your lab SOP, compound datasheets, and ethics approvals.
| Compound | Targets / pathways | Experimental notes |
|---|---|---|
| Palbociclib | CDK4/6 | HR+/HER2- endocrine combos; mind Rb loss conferring primary resistance. |
| Ribociclib | CDK4/6 | Cycle arrest readouts with endocrine/targeted partners; pair p-RB / Cyclin E1. |
| Olaparib | PARP1/2 | Synthetic lethality in gBRCA/HRD; watch stacked DDR toxicities. |
| Alpelisib | PI3Kα (PIK3CA-mutant) | PIK3CA-mutant subsets with endocrine partners; monitor hyperglycemia/rash. |
| Tamoxifen | ER (SERM; context-dependent agonism) | Classic endocrine tool; tissue/dose determines agonist vs antagonist phenotypes. |
| Fulvestrant | ER (degrader) | ER downregulation/resistance models; translate depot PK in animals carefully. |
| Everolimus | mTORC1 | Post-endocrine PI3K/AKT/mTOR axis probe; mind immunosuppression/metabolic AE. |