Specifications
- Pk:96 Tests
- Assay duration:One step
- Assay Type:Sandwich
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Human
- Target protein:CTRP4
- Description:Human CTRP4 ELISA kit
- Environmentally Preferable:
- 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:1 - 16 ng/ml
- Storage temperature:4 °C
- Sample volume:40 μl
- Sensitivity:0,028 ng/ml
- Regulatory status:RUO
Specifications
About this item
Human CTRP4 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human CTRP4 in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutess, with a single wash step
- Detection range: 1 to 16 ng/ml
- Sensitivity: 0,028 ng/ml
- Sample Type: Serum, plasma or other biological fluids
- Assay Precision: Intra-assay: CV <8%, Inter-assay: CV <10%
Human CTRP4 ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human CTRP4 in serum, plasma or other biological fluids. An antibody specific for CTRP4 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CTRP4 present in each sample is bound to the wells by the immobilised antibody. Biotinylated anti-CTRP4 antibody, which also binds the CTRP4 present in each sample, and Streptavidin-HRP, which binds the Biotinylated anti-CTRP4 antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated anti-CTRP4 antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. Colour develops in proportion to the amount of CTRP4 captured in each well. The colour development is stopped by addition of stop solution which changes the colour from blue to yellow and the intensity of the colour is then measured. The concentration of CTRP4 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.