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Invitrogen™ IgG (Total) Mouse Uncoated ELISA Kit with Plates
Specifically engineered for accurate and precise measurement of mouse IgG total in serum, plasma, and cell culture supernatants.
Supplier: Invitrogen™ 885040086
Includes: Capture Antibody Concentrate
Detection Antibody Concentrate
Mouse IgG1 isotype control (standard), lyophilized, 200ng/mL upon reconstitution
Phosphate Buffered Saline Concentrate (PBS)
Assay Buffer A Concentrate (PBS with 1% Tween 20 and 10% BSA)
Description
The Mouse Total IgG Uncoated ELISA Kit contains pre-matched antibody pairs, plates and reagents for performing quantitative enzyme linked immunosorbent assays (ELISA) to detect and quantify protein levels of mouse Total IgG. Wash Buffer and Stop Solution are needed to complete the ELISA reaction and are sold separately. Principle of the method ELISAs are designed to measure the amount of the target bound between a matched antibody pair. A target-specific antibody is coated to the bottom of the wells of a microplate, which is an overnight process. Samples, standards, or controls are then added into these wells and bind to the immobilized (capture) antibody. A sandwich is formed by the addition of the second (detector) antibody, a substrate solution is added that reacts with the enzyme-antibody-target complex to produce measurable signal. The intensity of this signal is directly proportional to the concentration of target present in the original specimen.
- The Mouse Total IgG Uncoated ELISA Kit contains pre-matched antibody pairs, plates and reagents for performing quantitative enzyme linked immunosorbent assays (ELISA) to detect and quantify protein levels of mouse Total IgG
- Wash Buffer and Stop Solution are needed to complete the ELISA reaction and are sold separately
- ELISAs are designed to measure the amount of the target bound between a matched antibody pair
- A target-specific antibody is coated to the bottom of the wells of a microplate, which is an overnight process
- Samples, standards, or controls are then added into these wells and bind to the immobilized (capture) antibody
- A sandwich is formed by the addition of the second (detector) antibody, a substrate solution is added that reacts with the enzyme-antibody-target complex to produce measurable signal
- The intensity of this signal is directly proportional to the concentration of target present in the original specimen
Specifications
| 1.56 to 100 ng/mL | |
| HRP | |
| Plasma, Serum, Supernatant | |
| ELISA | |
| Capture Antibody: Pre-titrated; purified antibody, Detection Antibody: Pre-titrated; biotin-conjugated antibody, Standard: Recombinant protein for generating standard curve and calibrating samples, 10X Coating Buffer: Buffer for plating the Capture Antibody, 5X ELISA/ELISPOT Diluent: Buffer for blocking and diluting the Detection Antibody and Enzyme, Enzyme: Pre-titrated Avidin-HRP, Substrate: 1X TMB Solution, Certificate of Analysis: Lot-specific instructions for dilution of antibodies and standards, 96 Well Plate: Corning Costar 9018 (included with product Cat. Nos. ending in suffixes -22; -76; -86) | |
| 10 x 96 Tests | |
| Plasma, 10 μL; Serum, 10 μL; Supernatant, 10 μL | |
| Immunoglobulin G, Immunoglobulin G total, IgG-total | |
| 1 hr. 45 min. |
| 1.56 ng/mL | |
| ELISA Kit | |
| Mouse | |
| Colorimetric Microplate Reader | |
| HRP | |
| RUO | |
| 2°C to 8°C | |
| Mouse | |
| 24 hr. 30 min. |
For Research Use Only