
Anti-Mouse IgG (whole molecule)−ATTO 488 antibody produced in goat
| Catalog Number | F10-0122 |
| Category | ATTO Dyes |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
IgG is the most abundant antibody in human serum. It is secreted by B cells andis found in blood. It consists of four polypeptide chains, made of two identical 50 kDa γ heavy (H) chains and two identical 25 kDa κ or λ light (L) chains, that is linked together by inter-chain disulfide bonds. IgG contains four isotypes IgG1, IgG2, IgG3 and IgG4.Immunoglobulin G (IgG) is a glycoprotein antibody that regulates immune responses such as phagocytosis and is also involved in the development of autoimmune diseases. Anti-Mouse IgG (whole molecule)-ATTO 488 antibody is specific for mouse IgG. The product is purified from goat anti-mouse IgG antiserum to remove all goat serum proteins, including immunoglobulins that do not specifically bind to mouse IgG. The antibody preparation is solid phase adsorbed with human serum proteins to ensure minimal cross reactivity.
Chemical Information
Product Specification
Application
Chemical Information
| NACRES | NA.46 |
Product Specification
| Properties Concentration | ~2 mg/mL, affinity isolated antibody, buffered aqueous solution |
Application
Goat anti-mouse IgG (whole molecule)−ATTO 488 antibody is a fluorescent secondary antibody reagent designed for immunofluorescence workflows, where it binds mouse IgG targets and provides an ATTO 488 fluorescence readout. The ATTO 488 dye is well matched to common blue-excitation microscope and flow cytometry setups, enabling visualization of mouse primary antibodies in fixed samples and fluorescent labeling of immunostained biomolecules. This reagent is produced as a whole-molecule antibody format, supporting robust signal generation in multicolor staining schemes that use mouse primary antibodies.
1. Immunofluorescence Microscopy
Goat anti-mouse IgG (whole molecule)−ATTO 488 antibody is widely used as a fluorescent secondary antibody to visualize mouse primary antibodies in fixed-cell and fixed-tissue immunostaining. Researchers in cell biology and microscopy workflows apply it to label target proteins, epitopes, and antibody-tagged biomolecules, with ATTO 488 emission enabling straightforward detection using standard FITC/488-channel filters. Whole-molecule secondary format helps maintain strong binding to mouse IgG, supporting clear localization patterns for confocal and widefield fluorescence imaging.
2. Flow Cytometry Antibody Staining
Goat anti-mouse IgG (whole molecule)−ATTO 488 antibody is used in flow cytometry staining strategies where mouse primary antibodies label cell-surface or intracellular targets, followed by ATTO 488 secondary detection. This approach is common in immunophenotyping and assay development because it allows flexible panel design by swapping mouse primaries while keeping a consistent ATTO 488 readout channel. The fluorescent secondary format also supports workflows where primary antibody conjugation is not desired, enabling standardized labeling across experiments and improving compatibility with typical 488-nm excitation instrumentation.
3. Western Blot Fluorescent Detection
Goat anti-mouse IgG (whole molecule)−ATTO 488 antibody is applicable for fluorescence-based immunodetection of mouse primary antibodies after protein separation, including membrane-based workflows where fluorescent secondary detection is preferred over enzymatic colorimetric systems. In these applications, the ATTO 488 signal provides a direct fluorescent readout for imaging-based quantification on compatible fluorescence scanners. Whole-molecule secondary antibodies are commonly selected to ensure strong binding to mouse IgG and consistent signal across blots containing mouse-reactive primary antibodies.
4. Multiplex Immunostaining Panels
Goat anti-mouse IgG (whole molecule)−ATTO 488 antibody supports multiplex immunofluorescence experiments by providing an ATTO 488 channel for mouse-primary detection alongside other fluorophores. Researchers use this reagent to build multicolor staining panels where mouse-targeted antibodies are detected with a dedicated green channel, while other primary antibodies are detected with spectrally distinct secondary reagents. This secondary antibody strategy helps streamline panel optimization by separating target recognition (mouse primary) from fluorescence assignment (ATTO 488 secondary), improving workflow consistency across experiments.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry