-
Reagents
- Flow Cytometry Reagents
-
蛋白质印迹试剂
- 免疫分析 试剂
-
Single-Cell Multiomics Reagents
- BD® AbSeq Assay
- BD Rhapsody™ 附件试剂盒
- BD® Single-Cell Multiplexing Kit
- BD Rhapsody™ TCR/BCR Next Multiomic Assays
- BD Rhapsody™ Targeted mRNA Kits
- BD Rhapsody™ Whole Transcriptome Analysis (WTA) Amplification Kit
- BD® OMICS-Guard Sample Preservation Buffer
- BD Rhapsody™ ATAC-Seq Assays
- BD® OMICS-One Protein Panels
-
Functional Assays
-
显微成像试剂
-
Cell Preparation and Separation Reagents
-
- BD® AbSeq Assay
- BD Rhapsody™ 附件试剂盒
- BD® Single-Cell Multiplexing Kit
- BD Rhapsody™ TCR/BCR Next Multiomic Assays
- BD Rhapsody™ Targeted mRNA Kits
- BD Rhapsody™ Whole Transcriptome Analysis (WTA) Amplification Kit
- BD® OMICS-Guard Sample Preservation Buffer
- BD Rhapsody™ ATAC-Seq Assays
- BD® OMICS-One Protein Panels
- China (Chinese)
-
改变地点/语言
Old Browser
Looks like you're visiting us from {countryName}.
Would you like to stay on the current location or be switched to your location?
BD Pharmingen™ PE Mouse anti-Human HLA-A2
克隆 BB7.2 (RUO)
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
Expression of PE anti-human HLA-A2 on lymphocytes from positive and negative donors
Human lymphocytes from either a positive or a negative donor were stained with PE anti-human HLA-A2 (clone: BB7.2; Cat. No. 558570) and compared to an isotype control (Cat. No. 555743). The overlay histograms show the HLA-A2 present on lymphocytes from the positive donor (right panel; solid line), but not on lymphocytes from a negative donor (left panel; solid line). In both figures, the isotype control is represented by the dashed line. Flow cytometry was performed on a BD FACSCalibur™ flow system.
监管状态图例
未经BD明确书面授权,严禁使用未经许可的任何商品。
准备和存储
商品通知
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
- Source of all serum proteins is from USDA inspected abattoirs located in the United States.
- For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
The monoclonal antibody BB7.2 specifically binds to the α subunit of the human leukocyte antigen-A2 (HLA-A2), a class I molecule of the major histocompatibility complex (MHC). The MHC gene locus encodes a group of highly polymorphic, cell-surface proteins that play a broad role in the immune response to protein antigens. MHC molecules bind and present small antigenic protein fragments to antigen-specific receptors expressed by T cells (TCR). Human (human leukocyte antigen/HLA) MHC molecules are comprised of two major classes, MHC class I and class II. Functionally, class I MHC molecules bind peptides derived from intracellular antigens (eg, viral and some bacterial antigens) which are specifically recognized by CD8+ T cells. Class II MHC molecules bind antigens derived from pathogens multiplying in intracellular vesicles and ingested extracellular bacteria, both of which are recognized by CD4+ T cells. TCR recognize processed peptides bound to the MHC as well as regions of the MHC molecule itself. CD4 and CD8 accessory molecules strengthen the formation of the TCR-MHC complex through their interaction with non-polymorphic regions of the MHC molecule.
研发参考 (3)
-
Bjorkman PJ, Saper MA, Samraoui B, Bennett WS, Strominger JL, Wiley DC. Structure of the human class I histocompatibility antigen, HLA-A2. Nature. 1987; 329(6139):506-512. (Biology). 查看参考
-
Brenner MB, McLean J, Yang SY, van der Poel JJ, Pious D, Strominger JL. Clonal T lymphocyte recognition of the fine structure of the HLA-A2 molecule. J Immunol. 1985; 135(1):384-390. (Biology). 查看参考
-
Brodsky FM, Parham P, Barnstable CJ, Crumpton MJ, Bodmer WF. Monoclonal antibodies for analysis of the HLA system. Immunol Rev. 1979; 47:3-6. (Biology). 查看参考
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.