SIRPG/CD172g Drug Discovery Landscape & Assay Solutions

Market Intelligence, Clinical Progress, and High-Purity Reagents for Next-Generation CD47 Axis Immunotherapy Development.

TarMart Solution Ecosystem & Related Targets

Comprehensive reagent toolkit for SIRPG/CD172g drug discovery. Select your modality below:

Component / Network Product Description Product Link
Antigen SIRPG ECD-Fc Fusion Protein
High purity (>95%), Endotoxin <1EU/ug. HEK293 Expressed (Native Glycosylation). Sequence Verified.
View SIRPG Products
Gene Delivery SIRPG Promise-ORF / Lentivirus
Full-length ORF for stable T-cell or NK-cell line construction.
View SIRPG Products
Benchmark Ab Anti-SIRPG (Sequence of Research Grade Clone)
Recombinant positive control for binding specificity.
View SIRPG Products
Validator SIRPG siRNA Set
For knockdown verification and specificity confirmation.
View SIRPG Products
SIRPA/CD172a SIRPA ECD-Fc Protein
Family homolog for selectivity screening (critical off-target check).
View SIRPA Products
CD47 CD47 Recombinant Protein
Ligand for binding competition and affinity characterization assays.
View CD47 Products
Critical Assay Challenge The TarMart Advantage (Technical Spec)
SIRP Family Selectivity (SIRPG vs SIRPA) Homolog Panel Proteins strictly verified by Mass Spec; Human SIRPG and SIRPA ECD-Fc available with distinct tag strategies for simultaneous detection
Cross-species Cyno/Mouse Eval Human/Mouse/Cyno ortholog proteins available with >95% purity; Sequence alignment verified for epitope conservation
CD47 Binding Affinity Quantification High-purity CD47 (H-tag/Avi-tag) for SPR/BLI; Theoretical MW confirmed by SDS-PAGE
Cell Surface Expression Validation Lentivirus Premade Particles (titer >1E8 TU/mL) for stable integration in Jurkat/Primary T-cell models
Lack of Controls Clinical Benchmark Antibodies (Biosimilars) and scrambled siRNA included

Live SIRPG R&D Tracker

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

Global Clinical Landscape & Future Outlook

The race for CD47/SIRP axis therapeutics is intensifying. First-generation pan-SIRP inhibitors can inadvertently block SIRPG on T cells, compromising anti-tumor immunity. The next wave of R&D is targeting SIRPG-selective blockade to enhance T-cell and NK-cell cytotoxicity without the systemic macrophage disruption associated with SIRPA targeting. SIRPG emerges as a compelling T-cell restricted alternative, offering distinct biology from the myeloid-focused SIRPA. As first-generation CD47 and SIRPA antibodies face toxicity and hematological challenges, the industry is pivoting toward alternative checkpoint nodes.

Competitive Modality & Indication Snapshot

Modality Representative Players Key Indications Critical Assay Need (Why TarMart?)
Anti-SIRPG mAb Early-stage biotech / Academic consortia Solid Tumors, Hematologic Malignancies Selectivity vs SIRPA (Need SIRPG/SIRPA ortholog panel)
SIRPG x CD3 Bispecific Preclinical developers T-cell Lymphoma, Solid Tumors Heterodimer Validation (Need full-length SIRPG Lentivirus)
SIRPG-targeted ADC Emerging IO platforms CD47-refractory Tumors Internalization Assay (Need high-purity ECD-Fc)
Combination (IO) Research consortia Refractory Solid Tumors Co-culture assay reagents (Need SIRPG + CD47 proteins)

Molecular Differentiation & Assay Strategy

Targeting SIRPG requires extreme selectivity and precise epitope mapping. Key strategies include:

  • Affinity & Epitope: Target unique IgV domain epitopes of SIRPG to avoid cross-reactivity with SIRPA.
  • Selectivity: Use homolog protein panels (SIRPA, SIRPB1) for rigorous counter-screening.
  • Cross-species: Validate binding to human, cynomolgus monkey, and mouse SIRPG for toxicology support.
  • Cell-based Assays: Lentiviral constructs for stable cell lines enable flow cytometry and functional co-culture studies.

TarMart provides the full toolkit: HEK293-expressed SIRPG ECD-Fc (native glycosylation, >95% purity), lentiviral particles, benchmark antibodies, siRNA, and SIRPA/CD47 proteins for seamless assay integration.