Pancreatic ductal adenocarcinoma (PDAC) is characterized by near-universal KRAS mutations (~95%), extensive desmoplastic stroma, and profound immunosuppressive tumor microenvironment. Current treatment relies on FOLFIRINOX and nab-paclitaxel regimens, while emerging approaches include KRAS G12D-targeted therapies, stromal remodeling, and vaccine-based immunotherapy. Early detection remains a critical unmet need.
Research Use Only (RUO)Not intended for diagnostic or therapeutic procedures.
Fig. 1 Key pathogenic pathways and research targets in pancreatic cancer. KRAS oncogenic signaling, desmoplastic stroma (FAP+ CAFs), mesothelin immunotherapy targets, and CA19-9 biomarker. abinScience product targets highlighted in orange.
abinScience provides validated antibodies, recombinant proteins, and ELISA kits for key pancreatic cancer research targets. All products are manufactured by our parent company AtaGenix Laboratories under ISO quality systems. Browse products below or contact us for custom antibody development.
KRAS (G12D/G12V/G12R) — KRAS mutations are present in approximately 95% of PDAC, with G12D being the most frequent. Anti-KRAS antibodies and mutation-specific reagents support oncogenic signaling research, KRAS-targeted therapeutic development, and downstream MAPK/PI3K pathway activation studies.
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CA19-9 (Sialyl Lewis A) — CA19-9 is the standard serum biomarker for PDAC diagnosis, treatment monitoring, and recurrence surveillance. Anti-CA19-9 antibodies and calibrator proteins enable ELISA assay development, IHC validation, and research into improved early detection biomarker panels.
→ Browse CA19-9 antibodies & proteins
Mesothelin (MSLN) — Mesothelin is overexpressed in PDAC and serves as a target for emerging immunotherapies including CAR-T cells and ADCs. Anti-mesothelin antibodies support IHC expression profiling, serum SMRP measurement, and therapeutic antibody competition studies.
→ Browse Mesothelin antibodies & proteins
FAP (Fibroblast Activation Protein) — FAP is highly expressed on cancer-associated fibroblasts (CAFs) in the desmoplastic PDAC stroma. Anti-FAP antibodies enable tumor microenvironment characterization, CAF isolation by flow cytometry, and research into FAP-targeted radioligand therapy and bispecific antibody approaches.
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1. Rahib L, et al. Projecting cancer incidence and deaths to 2030. Cancer Res. 2014;74(11):2913-2921. DOI
2. Conroy T, et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011;364(19):1817-1825. DOI
3. Waddell N, et al. Whole genomes redefine the mutational landscape of pancreatic cancer. Nature. 2015;518(7540):495-501. DOI
4. Von Hoff DD, et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369(18):1691-1703. DOI
5. Ho WJ, et al. The tumour microenvironment in pancreatic cancer. Nat Rev Gastroenterol Hepatol. 2020;17(8):487-505. DOI
Human
ELISA, FCM, WB
Human
IgG1, kappa
SAA2012
Human
ELISA, FCM
Human
IgG1, kappa
SAA2216
Human
FCM
Human
IgG1, kappa
MN14
Human
FCM
Human
IgG1, kappa
RG7813
Human
FCM
Human
IgG1, kappa
4D5V8
Human
ELISA, FCM, IHC, WB
Human
IgG1
5E5#
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
Fab Fused with a fragment of Pseudomonas exotoxin A.
LMB-100
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
IgG
BMS 986148
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
scFv-Human IgG1, kappa
MEDI4276
Human
ELISA, Bioactivity: FACS, Functional assay, Research in vivo
Human
IgG1-kappa