IgG1k, Murine, Isotype Control

Antibodies / Antibodies-Isotype Controls

-20°C

Supplied as a liquid in PBS, pH 7.4., 0.05% sodium azide.

Isotype Controls:
Isotype controls are a type of negative control designed to measure the level of non-specific background signal caused by primary antibodies,  based upon the tissue type of the sample. Non-specific binding of primary antibodies are typically caused by the following reasons:
• Non-specific Fc receptor binding to cells 
• Non-specific antibody interactions with cellular proteins or fluorochromes
• Non-specific binding of the antibody or fluorochromes to cellular components 
• Cell autofluorescence

Usually, the background signal is the result of immunoglobulins binding non-specifically to Fc receptors present on the cell surface. For example,  antibodies raised in mice, particularly those of the IgG2a isotype, will bind strongly to some human leukocytes regardless of the test antibody specificity. In this case you would need a mouse IgG2a isotype control for use with human cells or tissues. Isotype controls are most commonly used in flow cytometry experiments, but may also be used in immunohistochemistry. 

Selecting an Isotype Control:
Typically, an isotype control is matched to the host species and isotype of your specific primary antibody, the heavy chain (IgA, IgG, IgD, IgE, or IgM),  subclass and light chain (kappa, lambda) class of the primary antibody;   the same fluorochrome (PE, APC, etc.), and have the same F:P ratio. F:P is a measurement of how many fluorescent molecules are present on each antibody.

When using directly labeled primary antibodies, it is also necessary to make sure that the isotype control is conjugated to the same fluorochrome or label as the test antibody. It is not sufficient to use one with a spectrally similar fluorochrome.

Non-specific Binding:
To avoid non-specific binding, you also need to block Fc receptors on cell types, such as spleen cells, with FcR blocking reagents. Isotype controls should be used at the same concentration/dilution as the primary antibody. Isotype controls are mainly used to determine if the staining is real. Apart from isotype controls, unstained cells should always be included in the experimental set-up to monitor autofluorescence.

Applications for Isotype Controls:
Although isotype controls are mainly used in flow cytometry, they can be used as standard blocking agents and protein coating agents for other applications including immunofluorescence, immunocytochemistry, western blotting, and ELISA.

Mouse IgG1 myeloma cells (MOPC-21) were grown in mice and ascites fluid collected. The IgG1k was purified by a combination of column chromatography (Sephadex, and DEAE-ion exchange columns) and immunoaffinity chromatography. The resulting preparation was judged to be >96% pure by immuno electrophoresis (IEP) and SDS- PAGE. The purified protein is IgG1 kappa.

Source:
Mouse IgG1 myeloma cells from mouse serum.

Applications:
Suitable for use in ELISA (coating), or as a isotype control for ELISA, Dot Blot, Western Blot, and Immunohistochemistry. Other applications not tested.
Recommended Dilutions:
Optimal dilutions to be determined by the researcher.

Storage and Stability:
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months after receipt at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.