Professional Documents
Culture Documents
Immunophenotyping Kits For Flow Cytometry - Thermo Fisher Scientific - CO
Immunophenotyping Kits For Flow Cytometry - Thermo Fisher Scientific - CO
Home › Life Sciences › Cell Analysis › Flow Cytometry › Flow Cytometry Assays and Reagents › Immunophenotyping Kits for Flow Cytometry
Ready-to-Use Flow Cytometry Reagents Instrument agnostic—antibodies, protocol, and gating strategy are
compatible with any flow cytometer instrument equipped with violet 405 nm,
RNA Detection By Flow Cytometry
blue 488 nm, and red 633 nm lasers
Microbiology Assays for Flow Cytometry Comprehensive analysis strategy—a standardized data acquisition and
analysis plan is provided to perform flow cytometry characterization
5 Steps to Intracellular Flow Cytometry
Optimized antibody and reagent concentrations—panels contain the best
Immunophenotyping Kits for Flow combinations of antibodies and dyes for maximum sensitivity from a
Cytometry multicolor fluorescence experiment
Workflow
Step 1 Step 2
Stimulate cells from peripheral mononuclear cells Use buffer set included in kit for optimal intracellular
(PBMCs), lysed whole blood samples, or single-cell staining.
suspensions from human tissue for protein expression. Add LIVE/DEAD reagent to gate out debris and
This step is only required for eBioscience Essential artifacts.
Human Th1/Th17 Phenotyping Kit. Add labeled antibodies against cell surface and
intracellular markers to enable cell identification and
functionality characterization.
Figure 1. Overview of the T cell subset workflow. No extensive panel design is needed. You can just follow the protocol to generate your data.
The gating strategy gives guidance to find the correct cell populations when acquiring events. Results will show the percentage of T cells positive
or negative for the indicated markers.
Figure 2. T cells can be categorized into subset populations based on the particular immune response(s) they mediate. CD8+ T cells
directly kill infected or tumor cells via perforin and granzymes. CD4+ cells regulate other immune cells through adaptive immunity responses.
CD4+ cells can be stimulated to differentiate into multiple populations: for example, resulting Th1 cells influence macrophage and B cells and
resulting Th17 cells secret cytokines and other factors for an inflammatory response. The Treg population inhibits or downregulates the immune
response.
Filter sets:
eFluor 450 Pac Blue: 440/50 nm
eFluor 506: 510/50
PerCP-eFluor 710: 710/50 (695/40 acceptable)
FITC: 530/20
PE: 574/26
APC: 660/20
eBioscience™ Essential
A42923 100 reactions Contact Us › -
Human T-Cell Phenotyping Kit
eBioscience™ Essential
A42925 100 reactions Contact Us › -
Human Treg Phenotyping Kit
eBioscience™ Essential
A42927 Human Th1/Th17 Phenotyping 100 reactions Contact Us › -
Kit
Resources Support
Flow Cytometry Learning Center—Access flow Flow Cytometry Support Center—Find technical support
cytometry educational resources for better experiment recommendations for your flow cytometry workflows,
planning and execution. including tips for experimental setup and in-depth
troubleshooting help.
Flow Cytometry Panel Builder—Design your flow
cytometry panel with this online tool for a simplified, Flow Cytometry Protocols ›
customizable experience to fit your needs.
Contact us ›
5 Steps Resources
5 Steps to Intracellular Flow Cytometry
Not for resale. Super Bright Polymer Dyes are sold under license from Becton, Dickinson and Company.
Terms & Conditions Privacy Policy Price & Freight Policy Colombia