BD Multitest CD45RA/CD45RO/CD3/CD4. Catalog No Tests 20 µl/test

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Monoclonal Antibodies Detecting Human Antigens BD Multitest CD45RA/CD45RO/CD3/CD4 Catalog No. 340571 50 Tests 20 µl/test RESEARCH APPLICATIONS DESCRIPTION Specificity Antigen distribution Research applications include: Percentages and absolute counts of naive/memory T-helper cells 1-3 The CD45RA antibody recognizes a molecular weight of 220-kilodalton (kda) isoform of the leucocyte common antigen (LCA). 4 The CD45RA antigen is a member of the CD45 antigen family that also includes the CD45, CD45RB, and CD45RO antigens. 4 The CD45RO antibody, a member of the same CD45 family as CD45RA, recognizes a 180-kDa isoform of the LCA. 5-9 The CD45 antigen is a protein tyrosine phosphatase. 10 The CD3 antibody recognizes the epsilon chain of the CD3 antigen/t-cell antigen receptor (TCR) complex. 11 This complex is composed of at least six proteins that range in molecular weight from 20 to 30 kda. 12 The antigen recognized by the CD3 antibody is noncovalently associated with either α/β or γ/δ TCR (70 to 90 kda). 13 The CD4 antibody recognizes an antigen that interacts with class II molecules of the major histocompatibility complex and is the primary receptor for the human immunodeficiency virus. 14,15 The cytoplasmic portion of the antigen is associated with the protein tyrosine kinase p56 lck. 16 The CD4 antigen can regulate the function of the CD3 antigen/tcr complex. 17 CD4 also reacts with monocytes/macrophages that have an antigen density lower than that on helper/inducer T lymphocytes. 18 The CD45RA antigen is present on approximately 50% of CD4 + T lymphocytes, approximately 75% of CD8 + T lymphocytes, and on essentially all B lymphocytes and natural killer lymphocytes. 19 The suppressor inducer T-lymphocyte subset expresses the phenotype CD4 + CD45RA +. 19 The CD45RA antigen is expressed on naive T lymphocytes; antigen density decreases upon in vitro activation. 20 A selective loss of the CD4 + CD45RA + subset during active multiple sclerosis has been demonstrated. 21,22 In peripheral blood, the CD45RO antigen is present on approximately 40% of resting peripheral blood T lymphocytes, including the CD4 + and CD8 + subpopulations, as well as on most thymocytes and activated T lymphocytes. 5,6 It is also expressed on monocytes, macrophages, and granulocytes. 5,6 The CD45RO antigen is present at low density early in the T-lymphocyte maturation cycle. Upon activation by phytohemagglutinin or alloantigen, naive T lymphocytes first acquire CD45RO and then lose CD45RA. 6,7,23 When these activated T lymphocytes are rechallenged, the cells that exhibit a secondary response are primarily CD45RO +, leading to the concept that CD45RO + cells are a primed population of memory T lymphocytes. 6,7,23 The CD3 antigen is expressed on 61% to 85% of normal peripheral blood lymphocytes, 24 65% to 85% of thymocytes, 25 and on Purkinje cells in the cerebellum. 26 For Research Use Only. Not for use in diagnostic or therapeutic procedures. Becton, Dickinson and Company BD Biosciences 2350 Qume Drive San Jose, CA 95131 USA bdbiosciences.com ResearchApplications@bd.com 11/2014 23-3743-02

Clones Composition PROCEDURE REPRESENTATIVE DATA The CD4 antigen is expressed on the helper/inducer T-lymphocyte subset (CD3 + CD4 + ) that comprises 28% to 58% 24 of normal peripheral blood lymphocytes. 27 It is also present on 80% to 95% of normal thymocytes. 27 The CD4 antigen is present in low density on the cell surface of monocytes and in the cytoplasm of monocytes and macrophages (CD3 CD4 + ). 18 The CD45RA antibody, clone L48, is derived from hybridization of Sp2/0 mouse myeloma cells with spleen cells from BALB/c mice immunized with low-buoyant density human lymphocytes. The CD45RO antibody, clone UCHL-1, derived from hybridization of P3/NS-1/1-Ag4-1 mouse myeloma cells with spleen cells from BALB/c mice immunized with an interleukin-2 (IL-2)-dependent human T-cell line. 2 The CD3 antibody, clone SK7, 28-30 is derived from hybridization of NS-1 mouse myeloma cells with spleen cells from BALB/c mice immunized with human thymocytes. The CD4 antibody, clone SK3, 18,27,31 is derived from hybridization of NS-1 mouse myeloma cells with spleen cells from BALB/c mice immunized with human peripheral blood T lymphocytes. The CD45RA, CD3, and CD4 antibodies are each composed of mouse IgG 1 heavy chains and kappa light chains. The CD45RO antibody is composed of mouse IgG 2a heavy chains and kappa light chains. The BD Multitest reagent is supplied as a combination of CD45RA FITC, CD45RO PE, CD3 PerCP, and CD4 APC in 1.0 ml of phosphate buffered saline (PBS) containing bovine serum albumin (BSA), and 0.1% sodium azide. Visit our website (bdbiosciences.com) or contact your local BD representative for the lyse/wash protocol for direct immunofluorescence. 1. Pipet 20 µl of monoclonal antibody into a labeled tube. 2. Add 50 µl of whole blood. 3. Vortex gently to mix and incubate for 15 minutes in the dark at room temperature (20 C 25 C). 4. Add 1 ml of 1X BD FACS lysing solution (Cat. No. 349202) to the tube. The volume of BD FACS lysing solution recommended has been optimized for use with this reagent. 5. Vortex gently and incubate for 15 to 30 minutes in the dark at room temperature. If samples are not analyzed immediately, mix thoroughly before analysis. Flow cytometric analysis was performed on peripheral blood leucocytes using a BD FACSCalibur flow cytometer with a gate set on the CD3 + lymphocyte fraction. Laser excitation was at 488 nm and 635 nm. Representative data analyzed with a BD FACS brand flow cytometer is shown in the following figure. 23-3743-02 Page 2

SSC-H CD4 APC CD3 PerCP CD4 APC CD4 APC CD3 PerCP CD45RA FITC CD45RO PE HANDLING AND STORAGE WARNING CHARACTERIZATION WARRANTY Store vials at 2 C 8 C. Conjugated forms should not be frozen. Protect from exposure to light. Each reagent is stable until the expiration date shown on the bottle label when stored as directed. All biological specimens and materials coming in contact with them are considered biohazards. Handle as if capable of transmitting infection 32,33 and dispose of with proper precautions in accordance with federal, state, and local regulations. Never pipette by mouth. Wear suitable protective clothing, eyewear, and gloves. To ensure consistently high-quality reagents, each lot of antibody is tested for conformance with characteristics of a standard reagent. Representative flow cytometric data is included in this data sheet. Unless otherwise indicated in any applicable BD general conditions of sale for non-us customers, the following warranty applies to the purchase of these products. THE PRODUCTS SOLD HEREUNDER ARE WARRANTED ONLY TO CONFORM TO THE QUANTITY AND CONTENTS STATED ON THE LABEL OR IN THE PRODUCT LABELING AT THE TIME OF DELIVERY TO THE CUSTOMER. BD DISCLAIMS HEREBY ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY AND FITNESS FOR ANY PARTICULAR PURPOSE AND NONINFRINGEMENT. BD S SOLE LIABILITY IS LIMITED TO EITHER REPLACEMENT OF THE PRODUCTS OR REFUND OF THE PURCHASE PRICE. BD IS NOT LIABLE FOR PROPERTY DAMAGE OR ANY INCIDENTAL OR CONSEQUENTIAL DAMAGES, INCLUDING PERSONAL INJURY, OR ECONOMIC LOSS, CAUSED BY THE PRODUCT. REFERENCES 1. Connors M, Kovacs JA, Krevat S, Gea-Banacloche JC, Sneller MC, Flanigan M, Metcalf JA, Walker RE, Falloon J, Baseler M, Feuerstein I, Masur H, Lane HC. HIV infection induces changes in CD4 + T-cell phenotype and depletions within the CD4 + T-cell repertoire that are not immediately restored by antiviral or immune-based therapies. Nat Med. 1997;3: 533-640. 2. Benito J, Zabay J, Gil J, Bermejo M, Escudero A, Sánchez E, Fernández-Cruz E. Quantitative alterations of the functionally distinct subsets of CD4 and CD8 T lymphocytes in asymptomatic HIV infection: Changes in the expression of CD45RO, CD45RA, CD11b, CD38, HLA-DR, and CD35 antigens. J Acquir Immune Defic Syndr Hum Retrovirol. 1997;14:128-135. Page 3 23-3743-02

3. Lenki R, Bratt G, Holmberg V, Muirhead K, Sandstrom E. Indicators of T-cell activation: Correlation between quantitative CD38 expression and soluble CD8 levels in asymptomatic HIV+ individuals and healthy controls. Cytometry. 1998;33:115-122. 4. Cobbold S, Hale G, Waldemann H. Non-lineage, LFA-1 family, and leucocyte common antigens: new and previously defined clusters. In: McMichael AJ, ed. Leucocyte Typing III: White Cell Differentiation Antigens. New York: Oxford University Press; 1987:788-802. 5. Norton AJ, Ramsay AD, Smith SH, Beverley PC, Isaacson PG. Monoclonal antibody (UCHL-1) that recognizes normal and neoplastic T cells in routinely fixed tissues. J Clin Pathol. 1986;39:399-405. 6. Akbar AN, Terry L, Timms A, Beverley PC, Janossy G. Loss of CD45R and gain of UCHL-1 reactivity is a feature of primed T cells. J Immunol. 1988;140:2171-2178. 7. Smith SH, Brown MH, Rowe D, Callard RE, Beverley PC. Functional subsets of human helper-inducer cells defined by a new monoclonal antibody, UCHL-1. J Immunol. 1986;58:63-70. 8. Ledbetter JA, Tonks NK, Fischer EH, Clark EA. CD45 regulates signal transduction and lymphocyte activation by specific association with receptor molecules on T or B cells. Proc Natl Acad Sci USA. 1988;85:8628-8632. 9. Streuli M, Morimoto C, Schrieber M, Schlossman SF, Saito H. Characterization of CD45 and CD45R monoclonal antibodies using transfected mouse cell lines that express individual human leukocyte common antigens. J Immunol. 1988;141:3910-3914. 10. Tonks N, Charbonneau H, Diltz C, Fischer E, Walsh K. Demonstration that the leukocyte common antigen CD45 is a protein tyrosine phosphatase. Biochem. 1988;27:8695-8701. 11. van Dongen J, Krissansen G, Wolvers-Tettero I, et al. Cytoplasmic expression of the CD3 antigen as a diagnostic marker for immature T-cell malignancies. Blood. 1988;71:603-612. 12. Brenner MB, Groh V, Porcelli SA, et al. Plenary papers: structure and distribution of the human γδ T-cell receptor. In: Knapp W, Dörken B, Gilks WR, et al, eds. Leucocyte Typing IV: White Cell Differentiation Antigens. New York: Oxford University Press; 1989:1049-1053. 13. Clevers H, Alarcón B, Wileman T, Terhorst C. The T-cell receptor/cd3 complex: a dynamic protein ensemble. Annual Rev Immunol. 1988;6:629. 14. Maddon P, Dalgleish A, McDougal J, Clapham P, Weiss R, Axel R. The T4 gene encodes the AIDS virus receptor and is expressed in the immune system and the brain. Cell. 1986;47:333-348. 15. Dalgleish A, Beverly P, Clapham P, Crawford D, Greaves M, Weiss R. The CD4 (T4) antigen is an essential component of the receptor for the AIDS virus. Nature. 1984;312:763-767. 16. Rudd C, Burgess K, Barber E, Schlossman S. Monoclonal antibodies to the CD4 and CD8 antigens precipitate variable amounts of CD4/CD8-associated p56 lck activity. In: Knapp W, Dörken B, Gilks WR, et al, eds. Leucocyte Typing IV: White Cell Differentiation Antigens. New York: Oxford University Press; 1989:326-327. 17. Kurrle R. Cluster report: CD3. In: Knapp W, Dörken B, Gilks WR, et al, eds. Leucocyte Typing IV: White Cell Differentiation Antigens. New York: Oxford University Press; 1989:290-293. 18. Wood GS, Warner N, Warnke R. Anti-Leu-3/T4 antibodies react with cells of monocyte/macrophage and Langerhans lineage. J Immunol. 1983;131(1):212-216. 19. Morimoto C, Letvin NL, Distaso JA, Aldrich WR, Schlossman SF. The isolation and characterization of the human suppressor inducer T-cell subset. J Immunol. 1985;134:1508-1515. 20. Serra HM, Krowka JF, Ledbetter JA, Pilarski LM. Loss of CD45R (Lp220) represents a post-thymic T-cell differentiation event. J Immunol. 1988;140:1435-1441. 21. Rose LM, Ginsburg AH, Rothstein TL, Ledbetter JA, Clark EA. Selective loss of a subset of T helper cells in active multiple sclerosis. Proc Natl Acad Sci USA. 1985;82:7389-7393. 22. Sobel RA, Hafler DA, Castro EE, Morimoto C, Weiner HL. The 2H4 (CD45R) antigen is selectively decreased in multiple sclerosis lesions. J Immunol. 1988;140:2210-2214. 23. Picker LJ, Treer JR, Ferguson-Darnell B, Collins PA, Buck D, Terstappen L. Differential regulation of the peripheral lymph node homing receptor L-Selectin on T cells during the virgin to memory cell transition. J Immunol. 1993;150:1105-1121. 24. Reichert T, DeBruyère M, Deneys V, et al. Lymphocyte subset reference ranges in adult Caucasians. Clin Immunol Immunopath. 1991;60:190-208. 23-3743-02 Page 4

25. Lanier LL, Allison JP, Phillips JH. Correlation of cell-surface antigen expression on human thymocytes by multicolor flow cytometric analysis: Implications for differentiation. J Immunol. 1986;137:2501. 26. Garson JA, Beverly PCL, Coakham HB, Harper EJ. Monoclonal antibodies against human T lymphocytes label Purkinje neurons of many species. Nature. 1982;298:375. 27. Evans RL, Wall DW, Platsoucas CD, et al. Thymus-dependent membrane antigens in man: Inhibition of cell-mediated lympholysis by monoclonal antibodies to the TH 2 antigen. Proc Natl Acad Sci USA. 1981;78:544-548. 28. Haynes B. Summary of T-cell studies performed during the Second International Workshop and Conference on Human Leukocyte Differentiation Antigens. In: Reinherz E, Hayes B, Nadler L, Bernstein I, eds. Leukocyte Typing II: Human T Lymphocytes. New York: Springer-Verlag;1986:3-30. 29. Kan E, Wang C, Wang L, Evans R. Non-covalently bonded subunits of 22 and 28 kdad are rapidly internalized by T cells reacted with Anti Leu-4 antibody. J Immunol. 1983;131:536-539. 30. Knowles RW. Immunochemical analysis of the T cell-specific antigens. In: Reinherz EL, Haynes BF, Nadler LM, Bernstein ID, eds. Leukocyte Typing II: Human T Lymphocytes. New York: Springer- Verlag;1986:259-288. 31. Bernard A, Boumsell L, Hill C. Joint report of the First International Workshop on Human Leucocyte Differentiation Antigens by the investigators of the participating laboratories: T2 protocol. In: Bernard A, Boumsell L, Dausset J, Milstein C, Schlossman S, eds. Leucocyte Typing. Berlin: Springer-Verlag; 1984:25-60. 32. Protection of Laboratory Workers from Occupationally Acquired Infections; Approved Guideline Third Edition. Wayne, PA: Clinical and Laboratory Standards Institute; 2005. CLSI document M29-A3. 33. Centers for Disease Control. Perspectives in disease prevention and health promotion update: universal precautions for prevention of transmission of human immunodeficiency virus, hepatitis B virus, and other bloodborne pathogens in health-care settings. MMWR. 1988;37:377-388. PATENTS AND TRADEMARKS BD, BD Logo and all other trademarks are property of Becton, Dickinson and Company. 2014 BD Page 5 23-3743-02