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Specifications
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Rat
- Target protein:MCT1/Monocarboxylic Acid Transporter 1
- Description:Rat MCT1/monocarboxylic acid transporter 1 ELISA kit
- Size:96 tests
- Environmentally Preferable:
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Rat MCT1/Monocarboxylic Acid Transporter 1 ELISA Kit exhibits high specificity and excellent specificity for the detection of rat MCT1/Monocarboxylic Acid Transporter 1. No significant cross-reactivity or interference between MCT1/Monocarboxylic Acid Transporter 1 and analogues was observed.
- Detection Method:Colorimetric
- Time to Results:4 h 30 min
- Assay Principle:Quantitative
- Shelf Life:Store for 6 months at 4 °C
- Detection Range:0.156 - 10 ng/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:0.094 ng/ml
- Regulatory Status:RUO
- Cat. No.:76741-140
Specifications
About this item
Rat MCT1/Monocarboxylic Acid Transporter 1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat MCT1/Monocarboxylic Acid Transporter 1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 0.156 to 10 ng/ml
- Sensitivity: 0.094 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat MCT1 / Monocarboxylic Acid Transporter 1 ELISA Kit (A77333) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat MCT1 / Monocarboxylic Acid Transporter 1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for MCT1 / Monocarboxylic Acid Transporter 1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MCT1 / Monocarboxylic Acid Transporter 1 present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-MCT1 / Monocarboxylic Acid Transporter 1 Antibody, which binds the captured MCT1 / Monocarboxylic Acid Transporter 1 present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is proportional to the amount of MCT1 / Monocarboxylic Acid Transporter 1 captured in each well. The concentration of MCT1 / Monocarboxylic Acid Transporter 1 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.