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CD3 FITC/CD16+CD56 PE/CD45 PerCP

BD Tritest™ CD3 FITC/CD16+CD56 PE/CD45 PerCP

Product Details
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BD Tritest™
Human
Flow cytometry
IVD
Buffered saline with BSA and 0.1% sodium azide.


Description

BD Tritest™ CD3 fluorescein isothiocyanate (FITC)/CD16+CD56 phycoerythrin (PE)/CD45 peridinin chlorophyll protein (PerCP) is a threecolor direct immunofluorescence reagent for use with a suitably equipped flow cytometer to identify and determine the percentages and absolute counts of mature human T lymphocytes (CD3+) and natural killer (NK) (CD3CD16+CD56+) lymphocyte subsets in erythrocyte-lysed whole blood. When used with BD Trucount™ tubes, absolute counts of these populations can be enumerated from a single tube.

BD Tritest reagent and BD Trucount tubes can be used with the BD FACS™ Loader. The reagent can be used with or without an isotype control.

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 BD 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.

340300 Rev. 1
Components
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Description Clone Isotype EntrezGene ID
N/A N/A | IgG1, κ,IgG2b, κ,IgG1, κ,IgG1, κ N/A
340300 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 Diagnostics Use. 
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.