
Anti-Mouse IgG-ATTO 633 antibody produced in goat
| Catalog Number | F10-0139 |
| 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. Anti-mouse IgG (whole molecule) is purified from goat anti-mouse IgG antiserum to remove essentially all goat serum proteins, including immunoglobulins, which do not specifically bind to mouse IgG. The antibody preparation is solid phase adsorbed with human serum proteins to ensure minimal cross reactivity. Goat anti-mouse is conjugated to ATTO 633 NHS and purified by gel permeation chromatography and dialysis to remove unbound dye. ATTO 633-goat anti mouse IgG associates with mouse IgGs.
Chemical Information
Product Specification
Application
Chemical Information
| NACRES | NA.46 |
Product Specification
| Excitation | 636 |
| Emission | 650 |
| Properties Concentration | ~1 mg/mL IgG |
| Properties Quality Level | 100 |
| Storage | −20 °C |
Application
Anti-Mouse IgG-ATTO 633 antibody produced in goat is a fluorescently labeled secondary antibody designed for immunofluorescence workflows where mouse primary antibodies are detected with an ATTO 633 emission signal. Its goat origin supports common use in multiplex-compatible labeling schemes and routine microscopy sample preparation, enabling visualization of mouse IgG-containing targets in fixed samples and imaging assays. The ATTO 633 fluorophore provides a far-red readout that is frequently chosen to reduce spectral overlap with green-channel labels in multicolor experiments.
1. Immunofluorescence Microscopy
Anti-Mouse IgG-ATTO 633 antibody produced in goat is used as a fluorescent secondary antibody to visualize mouse primary antibody binding in fixed-cell and fixed-tissue immunostaining protocols. Researchers typically apply it for epifluorescence and confocal microscopy to generate robust spatial contrast of the antigen of interest, while leveraging the far-red ATTO 633 channel to support multicolor panels and clearer separation from common green fluorophores. In these workflows, the antibody format is selected for consistent labeling of mouse IgG and straightforward compatibility with established fixation and wash steps used in microscopy staining.
2. Flow Cytometry Detection
Anti-Mouse IgG-ATTO 633 antibody produced in goat supports fluorescence-based analysis of mouse antibody binding in cell-suspension assays, including immunophenotyping and antibody-based detection formats. In flow cytometry workflows, it serves as a secondary reagent to convert mouse primary antibody binding into a far-red fluorescence signal suitable for cytometer channel assignment and gating strategies. This reagent is commonly used in assay development where secondary labeling provides flexibility to standardize staining across different mouse primary antibodies while maintaining a consistent ATTO 633 readout.
3. Western Blot Immunodetection
Anti-Mouse IgG-ATTO 633 antibody produced in goat is applied for fluorescent immunoblotting workflows to detect mouse IgG-containing primary antibodies on membrane-bound targets. In these applications, the goat anti-mouse IgG-ATTO 633 conjugate enables far-red visualization on compatible fluorescence imaging systems, supporting quantitative densitometry workflows where fluorescent readouts are preferred over enzymatic colorimetric substrates. The secondary antibody format supports streamlined assay scaling across multiple blots while keeping the detection channel consistent through the ATTO 633 label.
4. Multiplex Immunostaining Panels
Anti-Mouse IgG-ATTO 633 antibody produced in goat is frequently incorporated into multicolor immunostaining experiments where far-red spectral separation helps manage cross-talk between fluorophores. Researchers use it to assign mouse primary antibody signals to the ATTO 633 channel while pairing with other primary/secondary combinations in the same sample to visualize multiple targets concurrently. This positioning is particularly useful for complex cellular imaging studies that require careful channel planning to maintain interpretable merged images and consistent labeling across experimental replicates.
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