
Anti-Mouse IgG-ATTO 594 antibody produced in goat
| Catalog Number | F10-0128 |
| Category | ATTO Dyes |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Immunoglobulin G (IgG) is a glycoprotein antibody that regulates immune responses such as phagocytosis and is also involved in the development of autoimmune diseases. Mouse IgGs have four distinct isotypes, namely, IgG1, IgG2a, IgG2b, and IgG3. IgG1 regulates complement fixation in mice. Affinity isolated antigen specific antibody is purified from goat anti-mouse IgG antiserum to remove essentially all goat serum proteins, including immunoglobulin. Goat anti-mouse IgG associates with mouse IgGs.
Chemical Information
Product Specification
Application
Chemical Information
| NACRES | NA.46 |
Product Specification
| Excitation | 603 |
| Emission | 625 |
| Properties Concentration | ~1 mg/mL protein |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
Anti-Mouse IgG-ATTO 594 antibody produced in goat is a fluorescent secondary antibody reagent designed for immunofluorescence workflows where mouse primary antibodies are detected using ATTO 594 labeling. The ATTO 594 fluorophore provides red-orange emission for multicolor microscopy and fluorescence-based assays, while the goat anti-mouse IgG specificity supports consistent signal generation from a wide range of mouse immunoreagents. This conjugate is commonly used in cell biology, protein localization studies, and assay development requiring robust secondary-antibody staining.
1. Immunofluorescence Microscopy
Anti-Mouse IgG-ATTO 594 antibody produced in goat is used as a secondary detection reagent in fluorescence microscopy to visualize mouse primary antibodies in fixed cells and tissue sections. Researchers in cell biology and biomaterials labs rely on this conjugate for mapping target protein localization, assessing expression patterns, and generating high-contrast fluorescence images with an ATTO 594 readout compatible with standard fluorescence microscope filter sets for red-channel imaging. The goat anti-mouse IgG format helps streamline staining workflows by providing a consistent binding interface for diverse mouse IgG-based primaries.
2. Flow Cytometry Staining
Anti-Mouse IgG-ATTO 594 antibody produced in goat supports fluorescence-based cytometry workflows where mouse primary antibodies are converted into a measurable red fluorescence signal for single-cell analysis. Immunophenotyping and protein expression studies commonly use this secondary antibody to label mouse IgG targets prior to acquisition on flow cytometers equipped with appropriate red/orange detection channels. In multiplex staining strategies, the ATTO 594 emission is selected to complement other fluorophores while maintaining clear separation between channels for gating and quantification.
3. Western Blot Immunodetection
Anti-Mouse IgG-ATTO 594 antibody produced in goat is applied for fluorescence-based immunodetection of proteins after transfer to membranes, offering an alternative to enzymatic secondary antibody systems. Protein analysis groups use this reagent to detect mouse IgG-bound targets with an ATTO 594 fluorescent signal that can be read on fluorescence imaging systems designed for labeled secondary antibodies. This approach is frequently used in protein expression profiling and method development where reproducible fluorescent readouts are preferred for densitometric analysis.
4. Multiplex Immunostaining Workflows
Anti-Mouse IgG-ATTO 594 antibody produced in goat is integrated into multicolor immunostaining panels where mouse primary antibodies must be detected alongside other targets labeled with spectrally distinct fluorophores. Imaging and assay development teams use this secondary antibody to assign a defined red-channel contribution from ATTO 594, enabling spatial co-localization studies and comparative quantification across multiple biomarkers within the same sample. Its goat anti-mouse IgG specificity supports consistent secondary binding across experiments, which is particularly valuable when building repeatable multiplex staining protocols.
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