Anti-Human HLA-DR/DP/DQ Antibody

Product Details


CloneIVA12
ApplicationFlow Cytometry
ReactivityHuman
FormatPurified
Target NameHLA-DR, HLA-DP, and HLA-DQ, MHC class II, pan HLA-II, pan MHC-II
IsotypeMouse IgG1
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
Protein Concentration0.5 mg/mL
Storage&HandlingThe antibody solution should be stored between 2°C and 8°C
See All FormatsClone IVA12

Background Information


Human HLA-DR, HLA-DP, and HLA-DQ are the three major classical human leukocyte antigen (HLA) class II molecules encoded within the major histocompatibility complex (MHC) on chromosome 6. These cell-surface glycoproteins are primarily expressed on professional antigen-presenting cells, including dendritic cells, macrophages, and B lymphocytes. Their principal function is to present peptides derived from extracellular proteins to CD4+ T helper cells, initiating and regulating adaptive immune responses. This process is essential for host defense against pathogens and for the development of immune memory.



Each HLA class II molecule consists of a polymorphic α (alpha) chain and β (beta) chain that together form a peptide-binding groove capable of accommodating peptides approximately 13–25 amino acids in length. The groove binds peptides generated in endosomal and lysosomal compartments following antigen processing. Peptide loading is facilitated by accessory molecules such as HLA-DM after removal of the invariant chain-derived CLIP peptide. The extensive genetic polymorphism of HLA-DR, HLA-DP, and HLA-DQ enables presentation of a broad repertoire of peptide ligands, including self and foreign antigens.



Specific HLA class II alleles are strongly associated with autoimmune diseases. For example, HLA-DR and HLA-DQ variants contribute to susceptibility to type 1 diabetes, rheumatoid arthritis, celiac disease, multiple sclerosis, and systemic lupus erythematosus. Certain HLA-DP alleles have also been linked to chronic hepatitis B outcomes and other immune-mediated disorders. These molecules are important in transplantation because mismatched HLA alleles increase the risk of graft rejection.



Therapeutically, HLA-DR, HLA-DP, and HLA-DQ are used in tissue matching for organ and stem cell transplantation, disease risk assessment, vaccine development, and immunotherapy. Their ability to present antigenic peptides also makes them attractive targets for antigen-specific tolerance strategies and personalized immunotherapies designed to modulate pathogenic T-cell responses while preserving protective immunity.

Isotype Control


Mouse IgG1 Isotype Control Antibody

Data Sheets


Anti-Human HLA-DR/DP/DQ Antibody TDS

Related Protocols


Flow Cytometry Protocol

Frequently Asked Questions


How do I determine the optimal antibody concentration/titer for my experiment?
We recommend titrating each new antibody lot on your own cell type and instrument, since optimal concentration depends on cell density, target expression level, and cytometer sensitivity. Suggested starting dilutions or test sizes (e.g., µg or µl per 10^6 cells) are provided on the product page as a starting reference point, not a fixed requirement.

Can these antibodies be used for intracellular or intranuclear staining, or only surface staining?
Intended use (surface, intracellular, or both) is specified per product, indicated under Application. The appropriate Related Protocol is linked for each product. If you need to detect both surface and intracellular markers in the same panel, confirm each antibody's compatibility with your fixation/permeabilization protocol before combining them.

What controls should I use alongside these antibodies?
Matched isotype controls (same host species, isotype, and conjugate) are available for most clones to help distinguish specific binding from background/non-specific staining and are linked on each product page. Unstained, single-color compensation, and fluorescence-minus-one (FMO) controls are also recommended, especially for multicolor panel design.

Can I combine InnoCyto Flow Cytometry antibodies into a multicolor panel?
Yes — antibodies across our catalog are designed to be panel-compatible, and conjugate options are offered specifically to support multiplexing. When building a panel, pair bright fluorophores with low-expression targets, avoid excessive spectral overlap, and confirm compensation is set up correctly for your specific fluorochrome combination. Use our Panel Builder to simplify the process.

Have a product or application question? Consult our FAQs or contact us.