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HLA DR antibody | YE2/36-HLK

Rat anti Human HLA DR

Product Type
Monoclonal Antibody
Clone
YE2/36-HLK
Isotype
IgG2a
Specificity
HLA DR

Product Code Applications Pack Size List Price Your Price Qty
MCA71R
Datasheet Datasheet Datasheet
SDS Safety Datasheet SDS
C F P * 0.25 mg loader
List Price Your Price
loader

Rat anti Human HLA DR antibody, clone YE2/36-HLK recognizes a monomorphic determinant of human HLA DR which is an MHC class II cell surface receptor expressed primarily on antigen presenting cells such as B lymphocytes, monocytes, macrophages and activated T lymphocytes.

The major histocompatibility complex (MHC) is a cluster of genes that are important in the immune response to infections. In humans, this complex is referred to as the human leukocyte antigen (HLA) region. There are 3 major MHC class II proteins encoded by the HLA which are HLA DP, HLA DQ and HLA DR.

Rat anti Human HLA DR antibody, clone YE2/36-HLK has also been reported to be cross reactive with mouse H-2 haplotypes b, d and q expressed by mouse strains including C57BL/6, DBA, and NZB (Brickell et al. 1981).

Target Species
Human
Product Form
Purified IgG - liquid
Preparation
Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
Buffer Solution
Phosphate buffered saline
Preservative Stabilisers
0.09%Sodium Azide
Carrier Free
Yes
Immunogen
EHR-B Ramos cells.
Approx. Protein Concentrations
IgG concentration 1.0 mg/ml
Fusion Partners
Spleen cells from immunised AO rats were fuzed with cells of the rat Y3 Ag1.2.3 myeloma cell line.
Regulatory
For research purposes only
Guarantee
12 months from date of despatch

This product is shipped at ambient temperature. It is recommended to aliquot and store at -20°C on receipt. When thawed, aliquot the sample as needed. Keep aliquots at 2-8°C for short term use (up to 4 weeks) and store the remaining aliquots at -20°C.

Avoid repeated freezing and thawing as this may denature the antibody. Storage in frost-free freezers is not recommended.

This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit the antibody protocols page.
Application Name Verified Min Dilution Max Dilution
Flow Cytometry 1/50 1/100
Immunohistology - Frozen
Immunohistology - Paraffin 1
  1. 1PLP fixation is recommended for optimal results, see Whiteland et al. for details
Where this product has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the product for use in their own system using appropriate negative/positive controls.
Flow Cytometry
Use 10ul of the suggested working dilution to label 106 cells in 100ul.

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Source Reference

  1. Brickell, P.M. et al. (1981) A monoclonal antibody to the HLA-DR product recognizes a polymorphic Ia determinant in mice.
    Immunology. 43: 493-501.

References for HLA DR antibody

  1. Cruchley, A.T. et al. (1987) Dual expression of the cell-surface antigens HLA-DR and CD1 (T6) by Langerhans cells in human buccal mucosa and skin.
    Arch Oral Biol. 32: 849-53.
  2. Thornhill, M.H. et al. (1989) Enhanced adhesion of autologous lymphocytes to gamma-interferon-treated human endothelial cells in vitro.
    Br J Exp Pathol. 70: 59-64.
  3. Whiteland, J.L. et al. (1995) Immunohistochemical detection of T-cell subsets and other leukocytes in paraffin-embedded rat and mouse tissues with monoclonal antibodies.
    J Histochem Cytochem. 43 (3): 313-20.
  4. Becker, D. et al. (1997) Flow-cytometric screening for the modulation of receptor-mediated endocytosis in human dendritic cells: implications for the development of an in vitro technique for predictive testing of contact sensitizers.
    J Immunol Methods. 203: 171-80.
  5. Jonuleit, H. et al. (2000) Induction of interleukin 10-producing, nonproliferating CD4(+) T cells with regulatory properties by repetitive stimulation with allogeneic immature human dendritic cells.
    J Exp Med. 192: 1213-22.
  6. Walter, W. et al. (2001) H2-Mbeta 1 and H2-Mbeta 2 heterodimers equally promote clip removal in I-A(q) molecules from autoimmune-prone DBA/1 mice.
    J Biol Chem. 276: 11086-91.
  7. Shimada, A. et al. (2006) Translocation pathway of the intratracheally instilled ultrafine particles from the lung into the blood circulation in the mouse.
    Toxicol Pathol. 34: 949-57.
  8. Colić, M. et al. (2006) Correlation between phenotypic characteristics of mononuclear cells isolated from human periapical lesions and their in vitro production of Th1 and Th2 cytokines.
    Arch Oral Biol. 51: 1120-30.
  9. View The Latest Product References
  10. Zuo, J. et al. (2009) The Epstein-Barr virus G-protein-coupled receptor contributes to immune evasion by targeting MHC class I molecules for degradation.
    PLoS Pathog. 5(1): e1000255.
  11. Hietbrink, F. et al. (2011) Intramedullary nailing of the femur and the systemic activation of monocytes and neutrophils
    World J Emerg Surg. 6: 34.
  12. Nguyen Hoang, A.T. et al. (2012) Dendritic cell functional properties in a three-dimensional tissue model of human lung mucosa.
    Am J Physiol Lung Cell Mol Physiol. 302 (2): L226-37.
  13. Klotz, B. et al. (2012) 1,25-Dihydroxyvitamin D3 Treatment Delays Cellular Aging in Human Mesenchymal Stem Cells while Maintaining Their Multipotent Capacity.
    PLoS One. 7: e29959.
  14. Thorne, A. et al. (2015) Tumor necrosis factor-α promotes survival and phenotypic maturation of poly(I:C)-treated dendritic cells but impairs their Th1 and Th17 polarizing capability.
    Cytotherapy. 17 (5): 633-46.
  15. Hietbrink F et al. (2015) The Impact of Intramedullary Nailing of Tibia Fractures on the Innate Immune System.
    Shock. 44 (3): 209-14.
  16. GarikipatiV, N.S. et al. (2018) Isolation and characterization of mesenchymal stem cells from human fetus heart.
    PLoS One. 13 (2): e0192244.
  17. Tripathy, N.K. et al. (2018) Cardiomyogenic Heterogeneity of Clonal Subpopulations of Human Bone Marrow Mesenchymal Stem Cells.
    J Stem Cells Regen Med. 14 (1): 27-33.

Flow Cytometry

RRID
AB_323671

MCA71R

165903 1806

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