Isotype Control

Isotype Controls - Determine Specific Binding

Isotype Controls —  Determine Specific Binding

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Isotype controls were developed for surface staining to ensure the specificity of antibody binding and that any observed staining is due to specific binding, rather than an artifact. They are raised against an antigen, such as keyhole limpet hemocyanin (KLH) or dinitrophenol (DNP), that is not found on the cell type or sample being analyzed. 

Isotype controls should be selected to match the host species, the Ig subclass, and the fluorophore of the primary antibody, and used at the same concentration as the primary antibody. As fluorophore conjugation to an antibody can vary between suppliers, we recommend purchasing the isotype control and primary antibody from the same supplier.  Note: Isotype controls may not be suitable for intracellular staining and should not be used to set gates. 

Determine Specific Binding

The debate about whether, when, and how to use isotype controls appears to be controversial  (Herzenberg L et al., Maecker HT and Trotter J.). You may not wish to use isotype controls, but if you do this article will give you an overview of what an isotype control is, when, and how to use it. Remember isotype controls are only one of a number of appropriate controls that will improve you flow cytometry data. For more information on controls in flow cytometry, we have a dedicated page, with a more detailed overview of controls in flow cytometry.

What Are Isotype Controls?

Unwanted background cell staining in flow cytometry can be a problem, especially when detecting novel or rare populations and when building panels containing multiple fluorophores. An isotype control is an antibody raised against an antigen not present on the cell type being analyzed (e.g. KLH or DNP) and has been specifically developed to determine the level of background surface staining.

An isotype control will:

  • Determine the non-specific binding of an antibody to Fc receptors found on monocytes, macrophages, dendritic, and B cells
  • Ensure the observed staining is due to specific binding rather than an artifact
  • Reveal other nonspecific binding of the antibody or fluorophores to cellular components (e.g. RPE and FITC, Takizawa et al. 1993, Hulspas et al. 2009)

How an Isotype Control can Help Determine Background Staining

The role of isotype controls in determining background staining can be observed in Figure 1a where no Fc block has been used (false positive cells circled in red) compared to Figure 1b where Fc block has been added. The specific F4/80 staining can be clearly seen in Figure 1C.

Fig.  1. J774 macrophages were stained for 30 minutes at 4oC in PBS containing 1% BSA (w/v) with CD11b FITC (MCA74F) and IgG2b Alexa Fluor®647 (MCA6006A647) a).

Fig. 1. J774 macrophages were stained for 30 minutes at 4oC in PBS containing 1% BSA (w/v) with CD11b FITC (MCA74F) and IgG2b Alexa Fluor®647 (MCA6006A647) A). In the absence of Fc block or B). In the presence of mouse Fc block (mouse Seroblock FCR, BUF041A).  In Fig 1a there is a significant population of cells positive (circled) with the A647 isotype control showing the Fc binding which disappears when Fc block is included, Fig 1B. Fig 1C shows specific F4/80 A647 (MCA497A647) staining. All data shown were gated on the 7-AAD negative, live population with the use of doublet discrimination.

The most appropriate isotype control matches:

  • The host species
  • Ig subclass
  • Fluorophore of the primary antibody

If you are using a mouse IgG1 monoclonal antibody that is conjugated to FITC, you should select a mouse IgG1 isotype control conjugated to FITC.

As the fluorophore conjugation to the antibody (known as the F/P ratio) can vary between suppliers, it is best to purchase the isotype from the same supplier as the primary. It is also advisable to use them at the same concentration as the primary antibody. If you want to calculate the F/P ratio of your antibodies we explain how in four easy steps.

Isotype controls have been optimized for surface staining. Intracellular staining can be affected by binding of both antibody and fluorophore to intracellular components, therefore choice of fluorophore and extra controls may be necessary. Remember isotype controls should not be used to determine compensation levels or the negative population.

Nonspecific antibody binding can be reduced by:

  • Blocking Fc receptors
  • Adding excess protein such as BSA to your buffer
  • Titration of your antibody
  • Gating out dead cells using a live/dead marker

To see our range of flow cytometry isotype controls with information on how and when to use them, download our isotype controls brochure. Alternatively you can use our handy search table located at the bottom of the page to find the right isotype control for your experiment.

Other Controls

As described, isotype controls are used to determine if the staining is specific. Apart from isotype controls, unstained cells should always be included in the experimental set-up to monitor autofluorescence. Additionally, for all multicolor flow cytometry experiments it is advisable to include compensation controls and fluorescence minus one (FMO) controls, which assist with identifying gating boundaries. We discuss other controls on our flow cytometry controls page.

Flow Negative Isotype Controls

    DescriptionSpecificityTargetFormatHostIsotypeClone Applications Citations Product Type Code Validation Types