NEGES0014 Bovine Serum Albumin (BSA) ELISA Kit
This Kit is for the quantitative measurement of Bovine Serum Albumin Residues in the Protein Purification Process, and End-Product (purified fermentation broth, cell culture supernatant, etc.).
NEGES0014 Bovine Serum Albumin (BSA) ELISA Kit
This Kit is for the quantitative measurement of Bovine Serum Albumin Residues in the Protein Purification Process, and End-Product (purified fermentation broth, cell culture supernatant, etc.).
Product Information | |
Cat. NO. | NEGES0014 |
Products Name | Bovine Serum Albumin (BSA) ELISA Kit |
Species | Bovine |
Product Size | 96 Tests |
Concentration | 0.5-32ng/mL |
Sensitivity | LOD: 0.03ng/mL; LOQ: 0.5ng/mL |
Principal | Sandwich ELISA |
Sample Volume | 100 ul |
Sample Type | ELISA Kit for the quantitative Measurement of Bovine Serum Albumin Residues in Protein Purification Process,and End-Product (purified fermentation broth, cell culture supernatant, etc.) |
Assay Time | 3 hours and 15 minutes |
Platform | Microplate Reader |
Conjugate | HRP |
Detection Method | Colorimetric |
Storage | 2-8°C |
Kit Components | ||
Reagents | Specification | Quantity |
Pre-Coated Microplate (Detachable) | 96 wells | 1 plate (Keep Sealed) |
Standard (Stock Solution) -10ug/ml | 10ul | 1 vial |
Standard S1 | 32 ng/mL | 1 vial |
Standard S2 | 8 ng/mL | 1 vial |
Standard S3 | 2 ng/mL | 1 vial |
Standard S4 | 0.5 ng/mL | 1 vial |
HRP-conjugated antibody(200×) | 80ul | 1 vial |
Diluent Buffer (10×) | 10ml | 1 vial |
TMB Substrates | 10ml | 1 vial (Avoid Light) |
Stop Solution | 10ml | 1 vial |
Wash Solution (100×) | 10ml | 1 vial |
Plate Sealer | 4 pieces | |
Instruction Manual | 1 |
Principle of the Assay |
This ELISA kit is applied to the double antibody sandwich Enzyme Linked Immunosorbent Assay to detect the concentration of BSA in samples. The microtiter plate has been pre-coated with anti-BSA antibody, standards or samples are then added to the microtiter plate wells and BSA if present, will bind to the antibody pre-coated wells under specific conditions. Then wash the plate to remove unbound substances, add the HRP-conjugated antibody, and incubate at room temperature (20-25°C) to form a double-antibody sandwich complex with the coated antibody, BSA, and detection antibody. Then a TMB substrate solution is added to the wells to incubate. TMB substrate solution turns blue after the oxidation of HRP, and finally turns to yellow immediately after adding the stop solution. Color of TMB substrate positively correlated with total BSA bound in the initial steps. The color is measured by spectrophotometrically with wavelength of 450nm. The concentration of BSA in samples is then determined by comparing the O.D. of the samples to the standard curve. |
Coefficient of Variance | Intra Variation:4-8% | ||
Inter Variation: 8-10% | |||
Specificity/ Cross-reactivity | Sample | Cross-Reactivity(%) | |
HSA | NA | ||
Fish Gelatin | NA | ||
Gelatin (Porcine/Bovine) | 6% |
Not available
Product: Not available
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