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BD Tritest™ CD4 FITC/CD8 PE/CD3 PerCP with BD Trucount™ Tubes
Product Details
BD Tritest™
Human
Flow cytometry
CE_IVD
Buffered saline with 0.1% sodium azide.
Description
BD Tritest™ CD4 fluorescein isothiocyanate (FITC)/CD8 phycoerythrin (PE)/CD3 peridinin chlorophyll protein (PerCP) is a three-color direct immunofluorescence reagent for use with a suitably equipped flow cytometer to identify and determine the absolute counts of mature human T lymphocytes (CD3+), helper/ inducer (CD3+CD4+) T lymphocytes, and suppressor/cytotoxic (CD3+CD8+) T lymphocytes in erythrocyte-lysed whole blood. When used with TruCOUNT™ Tubes, absolute counts of these populations can be enumerated from a single tube. BD Tritest reagent and TruCOUNT Tubes can be used with the FACS Loader.
Preparation And Storage
1. Store the reagent at 2–8°C. Do not use after the expiration date shown on the label.
2. Do not freeze the reagent or expose it to direct light during storage or incubation with cells. Keep the reagent vial dry.
3. Store TruCOUNT Tubes in their original foil pouch at 2–25°C. To avoid potential condensation, open the pouch only after it has reached room temperature and carefully reseal the pouch immediately after removing a tube. Examine the desiccant each time you open the pouch. If the desiccant has turned from blue to lavender, discard the remaining tubes. Use tubes within 1 hour after removal from the foil pouch and do not use beyond the expiration date indicated on the packaging.
342445 Rev. 1
Components
| Description | Quantity/Size | Part Number | Clone | Isotype | EntrezGene ID |
|---|---|---|---|---|---|
| CD3 PerCP | N/A | 50-7344 | SK3,SK1,SK7 | IgG1, κ,IgG1, κ,IgG1, κ | 920 |
342445 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.
For In Vitro Diagnostic Use.
23-22942-00
Documents are subject to revision without notice. Please verify you have the correct revision of the document, and always refer back to BD's eIFU website for the latest and most up to date information.