HLA-F抗体;HLA-F Antibody—艾普蒂

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     Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)    

  
  

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     Western blot analysis using HLA-F mouse mAb against Mouse Liver (1) tissue lysate.    

  
  

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     Flow cytometric analysis of Jurkat cells using HLA-F mouse mAb (green) and negative control (red).    

  
  

**Background of HLA-F Antibodies**

HLA-F, a non-classical major histocompatibility complex (MHC) class I molecule, differs from classical HLA-A, -B, and -C in its limited polymorphism and restricted tissue expression. Primarily expressed in immune-privileged sites (e.g., placenta) and under stress conditions (e.g., viral infection, cancer), HLA-F interacts with both innate and adaptive immune receptors, including NK cell receptors (e.g., KIR3DS1) and the CD94-NKG2A inhibitory complex. Its role in immune tolerance, viral defense, and pregnancy has sparked interest in therapeutic targeting.

HLA-F-specific antibodies are critical tools for studying its expression, structure, and function. Monoclonal antibodies (mAbs) against HLA-F enable detection in assays like flow cytometry, Western blot, and immunohistochemistry. These antibodies help elucidate HLA-F’s interaction mechanisms, such as its ability to present peptides or bind receptors in an open conformer form. Challenges include ensuring specificity due to structural similarities among MHC-I molecules.

Clinically, HLA-F is overexpressed in certain cancers (e.g., melanoma, breast cancer), correlating with immune evasion and poor prognosis. Antibodies targeting HLA-F are being explored for diagnostic and therapeutic applications, including blocking immune inhibitory pathways or enhancing antigen presentation. Recent studies suggest HLA-F may complement classical immune checkpoint inhibitors (e.g., anti-PD-1), offering novel combinatorial strategies. Ongoing research aims to clarify its dual roles in immune activation/suppression and optimize antibody-based interventions.