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Control γ1 FITC/γ2a PE

Control γ1 FITC/γ2a PE

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BD Simultest™
Phosphate buffered saline with gelatin and 0.1% sodium azide.


BD Simultest™ Control γ12a (IgG1 FITC/IgG2a PE) is a two-color direct immunofluorescence reagent for use as a negative control in flow cytometric immunophenotyping of erythrocyte-lysed whole blood (LWB). BD Simultest Control γ12a is used with BD Simulset™ software to set fluorescence-1 (FL1) and fluorescence-2 (FL2) quadrant markers around the unstained (negative) lymphocyte population and to estimate the amount of nonantigen-specific antibody binding (nonspecific staining) present, particularly that caused by Fc receptors. BD Simultest Control γ12a is for in vitro diagnostic use with BD Simultest in vitro diagnostic reagents.


• BD Simultest Control γ12a is for in vitro diagnostic use with BD Simultest in vitro diagnostic reagents.

• When stored at 2° to 8°C, antibody reagents are stable until the expiration date shown on the label. Do not use after the expiration date.

• The antibody reagent should not be frozen or exposed to direct light during storage or during incubation with cells.

• Incubation or centrifugation times or temperatures other than those specified may be a source of error.

• For optimal results, stain blood samples within 6 hours of venipuncture.

• Alteration in the appearance of the reagent, such as precipitation or discoloration, indicates instability or deterioration. In such cases, the reagent should not be used.

• The antibody reagents contain sodium azide as a preservative. However, care should be taken to avoid microbial contamination, which may cause erroneous results.

340041 Rev. 1
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描述 克隆 同型对照 EntrezGene ID
IgG2a PE X39 IgG2a, N/A
Mouse IgG1 Isotype Control FITC X40 IgG1, κ N/A
340041 Rev. 1
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研发参考 (8)

  1. A National Committee for Clinical Laboratory Standards. Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture (H3-A3). 1991. (Biology).
  2. Anderson CL, Looney RJ. Human leukocyte IgG Fc receptors. Immunol Today. 1986; 9:264-266. (Biology).
  3. Giorgi JV. Lymphocyte subset measurements: significance in clinical medicine. In: Rose NR, Friedman H, Fahey JL, ed. Manual of Clinical Laboratory Immunology. 3rd ed.. Washington, DC: American Society for Microbiology; 1986:236-246.
  4. Jackson AL, Warner NL. Rose NR, Friedman H, Fahey JL, ed. Manual of Clincial Laboratory Immunology, Third Edition. Washington DC: American Society for Microbiology; 1986:226-235.
  5. Landay AL, Muirhead KA. Procedural guidelines for performing immunophenotyping by flow cytometry. Clin Immunol Immunopath. 1989; 52:48-60. (Biology).
  6. McCarthy RC, Fetterhoff TJ. Issues for quality assurance in clinical flow cytometry. Arch Pathol Lab Med. 1989; 113:658-666. (Biology).
  7. National Committee for Clinical Laboratory Standards. Clinical Applications of Flow Cytometry: Quality Assurance and Immunophenotyping of Peripheral Blood Lymphocytes; Tentative Guideline. 1992; 1992. (Biology).
  8. Patrick CW, Swartz SJ, Harrison KA, Keller RH. Collection and preparation of hematopoietic cells for cell marker analysis. Lab Med. 1984; 15:659-665. (Biology).
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340041 Rev. 1

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.