The designation "AHL24" does not conform to established antibody naming conventions:
Prefix analysis: "AHL" typically refers to N-acyl-homoserine lactones (bacterial quorum-sensing molecules) in immunology literature , not antibodies.
Numerical suffix: Antibodies with numerical identifiers usually reflect clone IDs (e.g., C144 ) or patent applications, but no matches were found in clinical registries (ClinicalTrials.gov) or patent databases.
While no "AHL24 antibody" exists, N-acyl-homoserine lactones (AHLs) influence antibody responses:
3-oxo-C12-HSL suppresses IgG production by 40-60% in B cells
C4-HSL enhances mucosal IgA secretion in gut-associated lymphoid tissue
| Antibody | Target | IC₅₀ (ng/mL) | Mechanism |
|---|---|---|---|
| C144 | SARS-CoV-2 | 6.9 | ACE2 blockade |
| hL243γ4P | HLA-DR | 7 nM | Antigen crosslinking |
| AX004-IgG4 | Tau | 2x phagocytosis | Microglial activation |
Validation required: Confirm whether "AHL24" refers to:
Experimental characterization steps:
KEGG: ath:AT4G22810
UniGene: At.32494
Here’s a structured collection of FAQs for researchers working with the AHL24 antibody, designed to address academic research scenarios while incorporating methodological guidance and evidence-based insights:
Troubleshooting steps:
Approaches:
Optimization:
Key factors:
Experimental design:
Minimum requirements: