ADAM28 Drug Discovery Landscape & Assay Solutions

Market Intelligence, Clinical Progress, and High-Purity Reagents for Metalloproteinase-Targeted Therapy Development.

TarMart Solution Ecosystem & Related Targets

Comprehensive reagent toolkit for ADAM28 drug discovery. Select your modality below:

Component / Network Product Description Product Link
Antigen ADAM28 ECD-Fc Fusion Protein
Metalloproteinase & Disintegrin domains. HEK293 Expressed (Native Glycosylation). High Purity (>95% by SDS-PAGE). Endotoxin <1EU/µg. Sequence Verified.
View ADAM28 Products
Gene Delivery ADAM28 Promise-ORF / Lentivirus
Full-length ORF for stable cell line construction. Suitable for shedding assays and internalization studies.
View ADAM28 Products
Benchmark Ab Anti-ADAM28 (Research Reference)
Recombinant rabbit monoclonal positive control. Sequence Verified. Suitable for ELISA/Flow Cytometry.
View ADAM28 Products
Validator ADAM28 siRNA Set
Three pre-validated sequences for knockdown verification. Endotoxin-free.
View ADAM28 Products
Counter-Screen A ADAM17 (TACE)
Critical off-target metalloprotease for selectivity profiling. ECD-Fc Protein available.
View ADAM17 Products
Counter-Screen B ADAM10
Alpha-secretase activity control; also syndecan/Notch sheddase. Structurally homologous. ECD-Fc Protein available.
View ADAM10 Products
Related Target A CD44
Key downstream substrate in tumor metastasis signaling.
View CD44 Products
Related Target B IGFBP3
Cleavage target mediating cancer cell survival and proliferation.
View IGFBP3 Products
Related Target C ITGB1 (Integrin beta 1)
Physical interactor via ADAM28 disintegrin domain; pathway cross-talk.
View ITGB1 Products
Critical Assay Challenge The TarMart Advantage (Technical Spec)
Selectivity vs. ADAM17/TACE & ADAM10 (Safety Toxicity) Human ADAM17 & ADAM10 Ortholog Proteins available with >95% purity. Strictly verified by Mass Spectrometry for counter-screening panels.
Metalloproteinase Activity Conformation HEK293 Expression system ensures correct disulfide bond formation and cysteine-rich domain folding. Theoretical MW confirmed by reducing/non-reducing SDS-PAGE.
Cross-species Cyno/Mouse Evaluation Human/Mouse/Cyno ADAM28 ECD-Fc proteins available. Sequence alignment >85% identity verified prior to production.
Cell-surface Internalization & Shedding Kinetics Full-length ADAM28 lentivirus for stable transfection; preserves native membrane topology for flow cytometry and internalization assays.
Disintegrin Domain Off-target Integrin Binding High-purity domain truncation variants (Metalloprotease-only / Disintegrin-only) for epitope mapping and mechanism deconvolution.
False Positives in Binding Assays Validated siRNA included for specificity checks. Catalytic mutant (E→A) protein available for non-enzymatic binding studies.

Live ADAM28 R&D Tracker

Market data changes daily. Access the latest global pipeline status directly:

Global Clinical Landscape & Future Outlook

The race for ADAM28 therapeutics is intensifying. Overexpressed in breast, non-small cell lung (NSCLC), bladder, and prostate carcinomas, ADAM28 serves as a pivotal node in tumor metastasis and proliferation. Major players are shifting focus from broad-spectrum metalloprotease inhibitors to highly selective biologics, with first-generation ADC and antibody-based approaches entering preclinical validation. ADAM28 also represents an emerging frontier in inflammatory cell trafficking and tumor microenvironment remodeling. The next wave of R&D is targeting substrate-specific inhibition (e.g., IGFBP-3 shedding blockade) and selectivity engineering against closely related ADAM family members and disintegrin-domain-mediated off-target interactions, while avoiding ADAM17-mediated toxicity.

Competitive Modality & Indication Snapshot

Connect market trends to assay needs.

Modality Representative Players Key Indications Critical Assay Need (Why TarMart?)
ADC Emerging Biotech, Oncology Focused Labs, Academic Spin-offs Solid Tumors (NSCLC, Breast, Prostate) Internalization Assay (Need high-purity ECD-Fc with native conformation; lentivirus stable cell line)
Monoclonal Antibody Early Discovery Programs, Translational Oncology Labs Inflammation, Metastatic Carcinomas Selectivity Profiling (Need ADAM17/ADAM10 homolog proteins to avoid off-target; native glycosylation)
Small Molecule / Peptide Inhibitor Structure-Based Drug Design Groups, Specialty Pharma Refractory Solid Tumors Catalytic Activity Assay (Need properly folded zinc-binding domain; mutant vs WT proteins)
Bispecific Immuno-oncology Platforms Tumor Microenvironment Heterodimer binding validation (Need cross-reactive cyno/mouse ortholog proteins)