Anti-Human HLA-DR (MHC Class II) [Clone L243] — Purified in vivo GOLD™ Functional Grade

Anti-Human HLA-DR (MHC Class II) [Clone L243] — Purified in vivo GOLD™ Functional Grade

Product No.: H261

[product_table name="All Top" skus="H261"]

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Clone
L243
Target
HLA-DR
Formats AvailableView All
Product Type
Monoclonal Antibody
Alternate Names
Major Histocompatibility Class II, MHC class II, HLA-DR Monomorphic
Isotype
Mouse IgG2a
Applications
B
,
CyTOF®
,
Depletion
,
FC
,
IHC FF
,
in vivo
,
IP
,
PhenoCycler®
,
WB

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Antibody Details

Product Details

Reactive Species
Baboon
Chimpanzee
Cynomolgus Monkey
Marmoset
Rhesus Monkey
Squirrel Monkey
Canine
Human
Host Species
Mouse
Recommended Isotype Controls
Recommended Dilution Buffer
Immunogen
Unknown
Product Concentration
≥ 5.0 mg/ml
Endotoxin Level
< 1.0 EU/mg as determined by the LAL method
Purity
≥95% monomer by analytical SEC
>95% by SDS Page
Formulation
This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
Product Preparation
Functional grade preclinical antibodies are manufactured in an animal free facility using in vitro cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
Storage and Handling
Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles.
Country of Origin
USA
Shipping
Next Day 2-8°C
Applications and Recommended Usage?
Quality Tested by Leinco
FC The suggested concentration for this HLA-DR (Clone L243) antibody for staining cells in flow cytometry is ≤ 0.5 μg per 106 cells in a volume of 100 μl or 100μl of whole blood. Titration of the reagent is recommended for optimal performance for each application.
WB The suggested concentration for this HLA-DR (Clone L243) antibody for use in western blotting is 1-10 μg/ml.
Additional Applications Reported In Literature ?
IHC FF
CyTOF®
B
Depletion
IP
Additional Reported Applications For Relevant Conjugates ?
CODEX®
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
Clone L243 recognizes a conformational epitope on the human MHC class II molecule HLA-DRα, which depends on the correct folding of the αβ heterodimer1. It does not cross-react with HLA-DP or HLA-DQ.
Background
HLA-DR antibody, clone L243, recognizes the major histocompatibility complex (MHC) class II molecule Human Leukocyte Antigen - DR isotype (HLA-DR). MHC class II is constitutively expressed on human professional antigen-presenting cells (APCs), including macrophages/monocytes, dendritic cells (DCs), and B cells, and is induced on T cells upon activation2. HLA-DR consists of two transmembrane proteins, a 35 kDa α (heavy) chain and 29 kDa β (light) chain3 encoded by the HLA-DRA and HLA-DRB1, HLA-DRB3, HLA-DRB4, and HLA-DRB5 genes, respectively, located in the HLA complex of chromosome 6. The N-terminal α1 and β1 domains form the antigen-binding groove, which binds 13-25 aa peptides derived from exogenous antigens4. On APCs, MHC class II plays a critical role in the adaptive immune response by presenting phagocytosed antigens to helper CD4 T cells. The T cell receptor (TCR)/CD3 complex of CD4 T cells interacts with peptide-MHC class II, which induces CD4 T cell activation leading to the coordination and regulation of other effector cells. CD4 molecules also bind to MHC class II, which helps augment TCR signaling5. It has also been demonstrated that MHC class II express on activated T cells are capable of antigen presentation6 and can transduce signals into T cells, enhancing T cell proliferation and activity7. HLA-DR expression is a marker of T cell activation and correlates with disease activity in patients with autoimmune disease8 and rapid progression in HIV infection9. Specific alleles of HLA-DR are associated with autoimmune diseases, including rheumatoid arthritis10.
Antigen Distribution
HLA-DR is expressed on antigen-presenting cells, including macrophages, monocytes, DCs, and B cells, and activated T cells.
Ligand/Receptor
CD3/TCR, CD4
Function
Peptide presentation
PubMed
NCBI Gene Bank ID
Research Area
Immunology
.
Innate Immunity

Leinco Antibody Advisor

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In Vivo Applications of Clone L243 in Mice

Clone L243 is a mouse monoclonal antibody (IgG2a) that specifically binds to the human HLA-DR (MHC class II) antigen. While it is primarily designed for human studies, its use extends to certain mouse applications, especially in xenograft or humanized mouse models.

Direct In Vivo Use

Given that L243 is specific to human HLA-DR, its direct in vivo applications in wild-type mice are limited. Mice express their own MHC class II molecules (I-A, I-E), not human HLA-DR, so L243 does not recognize murine MHC class II and cannot be used for immunoprecipitation, cell depletion, or functional blockade in regular mice.

However, L243 can be used in vivo in humanized mouse models—mice engrafted with human cells or tissues expressing HLA-DR, such as human tumor xenografts or immune system humanized models. In these contexts, L243 can be used for:

  • Depletion of HLA-DR+ cells: Administering L243 in vivo may deplete human antigen-presenting cells (APCs) or tumor cells expressing HLA-DR, allowing researchers to study the role of these cells in immune responses or tumor progression.
  • Functional blockade: L243 can block HLA-DR-mediated antigen presentation, useful for investigating the role of HLA-DR in human immune cell activation and T cell responses within a humanized mouse context.
  • Cell tracking and phenotyping: L243 can be used to analyze the expression and function of human HLA-DR in engrafted human cells, providing insights into the behavior and differentiation of immune cells in vivo.

Indirect Applications

  • Genetic targeting: The variable regions of the L243 antibody have been cloned and used to engineer targeting units for DNA vaccines that direct immunogens specifically to HLA-DR+ human APCs in transgenic mice expressing human HLA-DR. For example, scFv derived from L243 has been incorporated into vaccine constructs to enhance antigen presentation in HLA-DR-transgenic mice, improving immune responses to vaccination.
  • Translational research: In studies where human cells or tissues are implanted into mice, L243 can be used to manipulate or assay those human cells in vivo, bridging preclinical and clinical research.

Typical Applications (Primarily In Vitro or Ex Vivo)

  • Flow cytometry: Phenotyping and sorting HLA-DR+ human cells in mouse tissues or blood after xenograft.
  • Immunohistochemistry: Detecting human HLA-DR expression in mouse tissue sections bearing human grafts.
  • Western blotting, immunoprecipitation, and immunofluorescence: Analyzing human HLA-DR protein levels or interactions in samples obtained from humanized mice.

Summary Table

ApplicationRegular MiceHumanized/Xenograft Mice
Depletion of HLA-DR+ cellsNoYes
Functional blockadeNoYes
Flow cytometry/IHCNoYes
Vaccine targetingTransgenicYes

Key Points

  • L243 is specific for human HLA-DR and does not recognize mouse MHC class II, so in vivo applications are restricted to mice bearing human cells or HLA-DR transgenes.
  • Humanized or xenograft mouse models are required for direct in vivo use of L243 in mice, enabling studies on human immune cell depletion, functional blockade, and antigen presentation.
  • Genetic targeting with L243-derived scFv can be used in transgenic mice expressing human HLA-DR for vaccine development and immune response studies.
  • In vivo applications in regular mice are not possible, but ex vivo and in vitro assays on human cells in mice are common.

In conclusion, clone L243’s main in vivo applications in mice are limited to models where human HLA-DR is present, such as in humanized or HLA-DR-transgenic mice. Here, it is used for targeted depletion, functional blockade, and immunological studies of human cells in a murine host.

The most commonly used antibodies and proteins with L243 (anti-HLA-DR) in the literature are other antibodies targeting cell lineage or differentiation markers and functional probes in multi-antibody panels, as well as those used in combination therapy research. Most notably:

  • Anti-CD20 antibodies (e.g., rituximab): Frequently combined with L243, especially in studies of B cell malignancies, due to the physical and functional coupling of CD20 and HLA-DR on B cells.
  • Other anti-HLA-DR clones (e.g., LB3.1): Used as comparators or validation clones in phenotyping and functional assays.
  • Anti-CD52 (e.g., alemtuzumab): Sometimes used in panel studies for characterizing immune cell populations or as combined therapeutic agents.
  • Lym-1 and Hu1D10: Alternative anti-HLA-DR antibodies studied in lymphoma and comparative preclinical experiments.
  • Cytokines and cytokine-coupled antibodies (e.g., IFNα, IFNα-antibody conjugates): Used to investigate additive or synergistic cytotoxic effects with L243, particularly on lymphoma cell lines.
  • Cell lineage markers: Antibodies such as anti-CD3, anti-CD4, anti-CD8, anti-CD19, and anti-CD45 are often included in multiparameter flow cytometry panels with L243 for immune profiling.
  • Isotype controls and secondary antibodies: Controls like mouse IgG2a and secondary antibodies (e.g., Alexa Fluor-conjugated goat anti-mouse IgG) are routinely paired with L243 in flow cytometry.

Key applications of these combinations include:

  • Multiparameter flow cytometry: For immune subset identification and activation profiling.
  • Therapeutic research in B-cell lymphomas: Evaluating combination therapies with rituximab and L243.
  • Functional studies: Assessing additive or synergistic effects (e.g., L243 + IFNα).

Other less commonly cited antibodies or proteins:

  • LAG-3: Protein studied for its direct and specific interaction with HLA-class II heterodimers, occasionally referenced for functional interaction studies with HLA-DR.
  • Negative and positive control antibodies: e.g., MN-14 (negative control), A20 (positive control) in cytotoxicity assessments.

In summary, frequently used antibodies/proteins with L243 include anti-CD20 (rituximab), other anti-HLA-DR clones, lineage markers (CD3, CD4, CD19), IFNα, and isotype/secondary controls.

Key findings from scientific literature citing clone L243 focus on its specificity, epitope recognition, non-cross-reactivity, and broad use in immune profiling of human and non-human primate cells:

  • Specificity and Epitope: Clone L243 is a mouse monoclonal antibody that binds specifically to a conformational epitope on the HLA-DR α-chain, which is only formed when the α and β chains of HLA-DR are correctly folded into a heterodimer. This specificity allows for highly reliable detection of native HLA-DR molecules on cells.

  • No Cross-Reactivity: L243 does not cross-react with other major human MHC class II molecules HLA-DP or HLA-DQ, further supporting its high selectivity for HLA-DR.

  • Target and Cellular Expression: The antibody detects HLA-DR, a key MHC class II molecule, which is constitutively expressed on professional antigen-presenting cells (APCs) including B cells, monocytes/macrophages, and dendritic cells, and can be induced on activated T cells and some epithelial cells.

  • Applications: L243 is widely used for:

    • Flow cytometry to identify and quantify HLA-DR+ cells in blood and tissues.
    • Immunohistochemistry and immunofluorescence for tissue staining.
    • Immunoprecipitation, western blotting, and cell depletion experiments.
    • Blocking mixed lymphocyte reactions in functional immune assays.
  • Reactivity Across Species: Clone L243 also cross-reacts with HLA-DR homologs in several non-human primate species and in dogs, broadening its utility in comparative and translational immunology research.

  • Biological Relevance: Research using L243 has contributed to understanding immune cell phenotyping, clinical assessment of immune activation (e.g., in transplantation, infection, or autoimmune disease), and the role of HLA-DR in antigen presentation to CD4+ T cells.

  • Publications and Impact: L243 is one of the most cited anti-HLA-DR clones in immunology literature, appearing in numerous peer-reviewed publications and referenced in diverse experimental contexts.

In summary, clone L243 is a gold-standard antibody for the reliable detection and functional study of HLA-DR in human and closely related species, with key findings supporting its utility in specific and sensitive immune phenotyping and research on antigen presentation.

The dosing regimens of clone L243, an antibody targeting human HLA-DR, can vary significantly across different mouse models. There is no universal dosing regimen for L243, as it is highly dependent on the specific experimental question, the degree of HLA-DR expression, and the type of mouse model being used (e.g., humanized vs. non-humanized models) .

Key Considerations:

  • Mouse Model Type: Different models might require different dosing strategies based on their specific characteristics, such as the presence of human HLA-DR expression.
  • Experimental Context: The dosing regimen should be tailored to the research objective, whether it involves cell depletion, immune modulation, or other purposes.
  • Empirical Determination: Researchers typically need to empirically determine the optimal dosing regimen for their specific study, often through trial and error.

Unfortunately, there isn't a standard dosing regimen available for clone L243 across various studies, as each research context is unique. Therefore, titration and optimization of the antibody dose are recommended to achieve the desired experimental outcomes.

References & Citations

1. Moro M, Cecconi V, Martinoli C, et al. (2005) BMC Immunol. 6:24
2. Holling TM, et al. (2004) Hum Immunol. 65(4):282-90
3. Mitaksov V, (2006) J Biol Chem. 281(15):10618-25
4. Wieczorek M, et al. (2017) Front Immunol. 8:292
5. Artyomov MN, et al. (2010) Proc Natl Acad Sci USA. 107(39):16916-16921
6. Barnaba V, et al. (1994) Eur J Immunol. 24(1):71-5
7. Di Rosa F, et al. (1993) Hum Immunol. 38(4):251-60
8. Viallard JF, et al. (2001) Clin Exp Immunol. 125(3):485-491
9. Langford SE, Ananworanich J, Cooper DA. (2007) AIDS Res Ther. 2007;4:11
10. Gough SC, Simmonds MJ. (2007) Curr Genomics. 8(7):453-465
B
CyTOF®
Depletion
Flow Cytometry
IHC FF
in vivo Protocol
Immunoprecipitation Protocol
PhenoCycler®
General Western Blot Protocol

Certificate of Analysis

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Disclaimer AlertProducts are for research use only. Not for use in diagnostic or therapeutic procedures.