BD, 559318, BD Pharmingen™ PE Rat IgG1, κ Isotype Control

Isotype: Rat IgG1, κ
Immunogen: Mouse immunoglobulin
Application: Flow cytometry, Isotype control (Routinely Tested), Intracellular staining (flow cytometry) (Tested During Development)
Vol. Per Test: 20 µl
RRID: AB_397216
Storage Buffer: Aqueous buffered solution containing BSA and ≤0.09% sodium azide.
Regulatory Status: RUO
Preparation And Storage: Preparation And Storage The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated with R-PE under optimum conditions, and unconjugated antibody and free PE were removed. Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze.
Recommended Assay Procedures: Recommended Assay Procedures Immunofluorescent Staining for Intracellular Cytokines: The PE-R3-34 immunoglobulin is a suitable rat IgG1 isotype control for assessing the level of background staining on paraformaldehyde-fixed/saponin-permeabilized mouse or human cells for flow cytometric analysis. This 100 Test Size formulation of the PE-conjugated R3-34 antibody has been pre-titrated to assure effective results as an Ig isotype control for our Test Sized PE-conjugated Rat IgG1 antibodies using 20µl/1 x 10^6 cells. The intracellular cytokine staining techinque and use of blocking controls are described in detail by C. Prussin and D. Metcalfe. For specific methodology, please visit the protocols section or chapter on intracellular staining in the Immune Function Handbook, both of which are posted on our web site, www.bdbiosciences.com. Important Note: This pre-titered antibody solution does not contain a cell permeabilization agent. It is necessary to include a cell permeabilization agent when using the pre-titered antibody solution to stain fixed and permeabilized cells. BD Perm/Wash™ Buffer (Cat. No. 554723) contains the permeabilization agent saponin and is useful for this purpose as described in the Usage section below. Usage 1. Resuspend 1 x 10^6 fixed and permeabilized cells in 20 µl of the pre-titered antibody solution and 30 µl of 1 x BD Perm/Wash™ Buffer (Cat. No. 554723). 2. Incubate the cell suspension for 15 minutes (at RT or 4°C). 3. Wash twice in 100 µl of 1 x BD Perm/Wash Buffer (Cat. No. 554723).