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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Major histocompatibility complex class II DR beta 1 (HLA-DRB1) is a transmembrane glycoprotein encoded by the HLA-DRB1 gene that forms the beta chain of the HLA-DR antigen-presenting receptor complex. HLA-DRB1 Antibody for FACS enables flow cytometry detection of HLA-DR beta chain expression on the surface of immune cells, supporting identification and characterization of antigen-presenting cell populations in suspension-based assays. HLA-DR molecules belong to the MHC class II family and function as heterodimeric receptors composed of an alpha chain encoded by HLA-DRA and a beta chain encoded by HLA-DRB genes. These receptors bind peptides derived from extracellular proteins that have been processed within endosomal compartments and present them to CD4-positive helper T lymphocytes. Through this mechanism, HLA-DR plays a central role in adaptive immune activation and coordination of immune responses. Expression of HLA-DR is therefore characteristic of professional antigen-presenting cells including B lymphocytes, dendritic cells, macrophages, and activated monocytes. Flow cytometry analysis is widely used to quantify and phenotype immune cell populations based on surface antigen expression. Antibodies recognizing HLA-DRB1 allow researchers to identify antigen-presenting cells within heterogeneous cell suspensions and to monitor immune activation states. Because HLA-DR expression increases during immune activation and inflammatory responses, measurement of HLA-DR levels by flow cytometry provides important insight into immune regulation, antigen presentation capacity, and immune cell differentiation. In flow cytometry experiments, antibodies such as mouse monoclonal clone SPM423 bind HLA-DR beta chain molecules expressed on the plasma membrane of immune cells. Fluorescent secondary antibodies or directly conjugated detection reagents enable quantification of HLA-DR-positive cell populations and analysis of expression levels across different immune subsets. This approach supports multiparameter flow cytometry studies examining immune cell phenotyping, antigen presentation dynamics, and immune activation pathways in human cell samples.
Optimal dilution of the HLA-DRB1 Antibody for FACS SPM423 should be determined by the researcher.
1. Staining of formalin-fixed tissues is enhanced by boiling tissue sections in pH 9 10mM Tris with 1mM EDTA for 10-20 min followed by cooling at RT for 20 min
2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.
Activated human peripheral blood mononuclear cells were used as the immunogen for the anti-HLA-DRB1 antibody.
Store the HLA-DRB1 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
HLA-DR beta antibody, HLA-DRB1 antibody, MHC class II DR beta antibody, HLA class II histocompatibility antigen DR beta antibody
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