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BD™ HLA-B27 Kit
(IVD)
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Description
The BD™ HLA-B27 system is a qualitative two-color direct immunofluorescence method for the rapid detection of HLA-B27 antigen expression in erythrocyte-lysed whole blood (LWB) using the BD FACSCanto™ family of flow cytometers, or the BD FACSCalibur™, BD FACSort™, or BD FACScan™ flow cytometer. Contents: Anti-HLA-B27 FITC / CD3 PE, HLA-B27 calibration beads, and BD FACS™ Lysing Solution.
The BD™ HLA-B27 system is a qualitative two-color direct immunofluorescence method for the rapid detection of HLA-B27 antigen expression in erythrocyte-lysed whole blood (LWB) using the BD FACSCanto™ family of flow cytometers, or the BD FACSCalibur™, BD FACSort™, or BD FACScan™ flow cytometer. Contents: Anti-HLA-B27 FITC / CD3 PE, HLA-B27 calibration beads, and BD FACS™ Lysing Solution.
Preparation And Storage
• Store Reagent A and Reagent C upright at 2° to 8°C. Do not use after the expiration date shown on the label.
• Store Reagent B, undiluted, at 2° to 25°C. When diluted, store at room temperature (20° to 25°C) for up to one month.
• Do not freeze the reagents or expose them to direct light during storage or incubation with cells. Keep reagent vials dry.
Description | Quantity/Size | Part Number | |
---|---|---|---|
Anti-HLA-B27 FITC / CD3 PE | 50 Tests (1 ea) | 91-0177 | N/A |
HLA-B27 calibration beads | 50 Tests (1 ea) | 91-0176 | N/A |
BD FACS™ Lysing Solution | 50 Tests (1 ea) | 91-0175 | N/A |
Development References (14)
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Centers for Disease Control. Update: universal precautions for prevention of transmission of human immunodeficiency virus, hepatitis B virus, and other bloodborne pathogens in healthcare settings. MMWR. 1988; 37:377-388. (Biology).
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Dausset J. The major histocompatibility in man, Past, present, and future concepts. Science. 1981; 213:1469-1474. (Biology).
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Haynes BF. Summary of T-cell studies performed during the Second International Workshop and Conference on Human Leukocyte Differentiation Antigens. In: Reinherz EL. Ellis L. Reinherz .. et al., ed. Leukocyte typing II. New York: Springer-Verlag; 1986:3-30.
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Johnson J, Garbutt J, Nelson K. A monoclonal antibody specific for HLA-B27. Human Immunol. 1985; 134-135. (Biology).
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Kan EAR, Wang CY, Wang LC, Evans RL. Noncovalently bonded subunits of 22 and 28 kd are rapidly internalized by T cells reacted with Anti–Leu-4 antibody. J Immunol. 1983; 131:536-539. (Biology).
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Knowles RW. Immunochemical analysis of the T-cell–specific antigens. In: Reinherz EL. Ellis L. Reinherz .. et al., ed. Leukocyte typing II. New York: Springer-Verlag; 1986:259-288.
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Ledbetter JA, Evans RL, Lipinski M, Cunningham-Rundles C, Good RA, Herzenberg LA. Evolutionary conservation of surface molecules that distinguish T lymphocyte helper/inducer and cytotoxic/suppressor subpopulations in mouse and man. J Exp Med. 1981; 153(2):310-323. (Biology). View Reference
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Levering WH, Wind H, Sintnicolaas K, Hooijkaas H, Gratama JW. Flow cytometric HLA-B27 screening: cross-reactivity patterns of commercially available anti-HLA-B27 monoclonal antibodies with other HLA-B antigens. Cytometry B Clin Cytom. 2003; 54B:28-38. (Biology).
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Lopez-Larrea C, Gonzalez-Roces S, Alvarez V. HLA-B27 structure, function, and disease association. Curr Opin Rheumatol. 1996; 8:296-308. (Biology).
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Müller H, Albrecht J, Schabel A. New aspects in HLA-typing by use of monoclonal antibodies and calibrated flow cytometry. Fresenius A Anal Chem. 1988; 330:341. (Biology).
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NCCLS document. 2001. (Biology).
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Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture–Fourth Edition; Approved Standard. NCCLS document H3-A4. 1998. (Biology).
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Seipp MT, Erali M, Wies RL, Wittwer C. HLA-B27 typing: evaluation of an allele-specific PCR melting assay and two flow cytometric antigen assays. Cytometry B Clin Cytom. 2005; 63:44119. (Biology).
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Taurog JD, El-Zaatari FA. In vitro mutagenesis of HLA-B27. Substitution of an unpaired cysteine residue in the α 1 domain causes loss of antibody-defined epitopes. J Clin Invest. 1988; 82:987-992. (Biology).
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.
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