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Description
Human APOA1/Apolipoprotein A1 protein participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase. Defects in APOA1/Apolipoprotein A 1 are a cause of familial hypoalphalipoproteinemia and the low HDL levels as well as amyloidosis van Allen type disease.
- In this ELISA kit, an APOA1/Apolipoprotein A1 specific antibody has been pre-coated onto 96-well plates and blocked
- Standards or test samples are added to the wells and subsequently an APOA1/Apolipoprotein A1 specific biotinylated detection antibody is added and followed by washing with wash buffer
- Afterwards, Streptavidin-Peroxidase Complex is added and unbound conjugates are washed away with wash buffer
- TMB is then used to visualize Streptavidin-Peroxidase enzymatic reaction
- TMB is catalyzed by Streptavidin-Peroxidase to produce a blue color product that changes to yellow after adding an acidic stop solution
- The density of yellow coloration is directly proportional to the amount of APOA1/Apolipoprotein A1 captured in the plate
- Sensitivity: 0.188 ng/mL in ELISA assays
Specifications
Specifications
| Assay | Sandwich Assay |
| Conjugate | APO A1 |
| Cross Reactivity | None |
| Immunoassay Kit Format | 96-well Plate |
| Label Type | Biotin |
| Product Line | MP Biomedicals |
| Product Type | ELISA Kit |
| Protein Family | Apolipoprotein |
| Sample Type | Plasma, Serum, Tissue Homogenates |
| Specificity | No Cross-reactivity to Other Antigens |
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Safety and Handling
Unless specified otherwise, MP Biomedical™'s products are for research or further manufacturing use only, not for direct human use.
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