Specifications
- Assay duration:One step
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:MRPL53
- Description:Human MRPL53 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:125 - 2000 ng/L
- Storage Temperature:4 °C
- Sample Volume:40 μl
- Sensitivity:14.66 ng/L
- Regulatory Status:RUO
- Cat. No.:77216-588
Specifications
About this item
Human MRPL53 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MRPL53 in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutes, with a single wash step
- Detection range: 125 to 2000 ng/L
- Sensitivity: 14.66 ng/L
- Sample type: Serum, plasma or other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Human MRPL53 ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human MRPL53 in serum, plasma or other biological fluids. An antibody specific for MRPL53 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MRPL53 present in each sample is bound to the wells by the immobilized antibody. Biotinylated Anti-MRPL53 antibody, which also binds the MRPL53 present in each sample, and Streptavidin-HRP, which binds the Biotinylated Anti-MRPL53 antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated Anti-MRPL53 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 MRPL53 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 MRPL53 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.