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Alert : The site is undergoing maintenance. Some functionality including sign-in may be impacted
Saturday, February 21, 3:00 pm through Tuesday, March 03, 9:00 pm (PST), 2026
Ordering can continue through fax and phone.
Contact usAlert : The site is undergoing maintenance. Some functionality including sign-in may be impacted
Saturday, February 21, 3:00 pm through Tuesday, March 03, 9:00 pm (PST), 2026
.Ordering can continue through fax and phone.
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The selection of an appropriate isotype control is essential for every flow cytometry experiment. Isotype control Abs that have no relevant specificity help to distinguish non-specific "background" staining from specific antibody staining. There are three main factors that contribute to the levels of background staining associated with a primary Ab: 1) binding to Fc receptors on target cells, 2) non-specific protein interactions with cellular proteins, lipids, or carbohydrates, and 3) cell autofluorescence. All of these factors can greatly vary depending on the target cell type and the isotype of the primary Ab. Thus, isotype controls need to be matched to the specific primary Abs (species and isotype, including heavy and light chains) being used in order to accurately determine the level of specific staining by the primary Ab. The most common monoclonal Ab isotypes are IgG1, IgG2a, IgG2b, IgG3, IgM, and IgA. Recommended isotype controls can often be found on the Technical Data Sheets for primary antibodies.
Skip to Step B if you already know the isotype and origin species of your primary Ab.
For optimal results, use the isotype control product at the same concentration as your primary Ab.