Specifications
- Assay duration:One step
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:MT-RNR1
- Description:Human MT-RNR1 ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma or other biological fluids
- Detection Method:Colorimetric
- Time to Results:1 h 30 min
- Shelf Life:Store for 6 months at 4 °C
- Detection Range:50 - 800 ng/L
- Storage Temperature:4 °C
- Sample Volume:40 μl
- Sensitivity:4.08 ng/L
- Regulatory Status:RUO
- Cat. No.:77213-658
Specifications
About this item
Human MT-RNR1 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MT-RNR1 in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutes, with a single wash step
- Detection range: 50 to 800 ng/L
- Sensitivity: 4.08 ng/L
- Sample type: Serum, plasma or other biological fluids
- Assay precision: Intra-assay: CV <8%, Inter-assay: CV <10%
Human MT-RNR1 ELISA kit (A312439) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human MT-RNR1 in serum, plasma or other biological fluids. An antibody specific for MT-RNR1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MT-RNR1 present in each sample is bound to the wells by the immobilized antibody. Biotinylated Anti-MT-RNR1 antibody, which also binds the MT-RNR1 present in each sample, and Streptavidin-HRP, which binds the Biotinylated Anti-MT-RNR1 antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated Anti-MT-RNR1 antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. Color develops in proportion to the amount of MT-RNR1 captured in each well. The color development is stopped by addition of stop solution which changes the color from blue to yellow and the intensity of the color is then measured. The concentration of MT-RNR1 in the samples can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.