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Human TPTE ELISA Kit
  ANTIA302797-96
 :  Antibodies.com
New Product
 :  
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Human TPTE ELISA Kit
  ANTIA302797-96
 :  Antibodies.com
New Product
 :  

 

  • Pk:
    96 Tests
  • Assay duration:
    Multiple steps
  • Assay Type:
    Sandwich
  • Format:
    Pre-coated
  • Primary antibody reactivity:
    Human
  • Target protein:
    TPTE
  • Description:
    Human TPTE ELISA kit
  • Sample type:
    Serum, plasma, tissue homogenates, and other biological fluids
  • Cross reactivity:
    Human TPTE ELISA Kit exhibits high specificity and excellent specificity for the detection of human TPTE. No significant cross-reactivity or interference between TPTE and analogues was observed.
  • Detection method:
    Colorimetric
  • Time to Results:
    4 h 30 min
  • 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

 

 

Human TPTE ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human TPTE in serum, plasma, tissue homogenates, and other biological fluids.

  • Ready-to-use ELISA kit
  • Assay precision: Intra-assay: CV <8%, Inter-assay: CV <10%

Human TPTE ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human TPTE in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for TPTE has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the TPTE present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-TPTE Antibody, which binds the captured TPTE 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 visualise 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 TPTE captured in each well. The concentration of TPTE can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.

 : This is a ready-to-use ELISA kit that contains: Pre-coated 96 well microplate, lyophilised standard, sample dilution buffer, biotinylated detection antibody (100X), antibody dilution buffer, HRP-Streptavidin conjugate (SABC) (100X), SABC dilution buffer, TMB substrate, stop solution, wash buffer (25X), plate sealers, foil pouch, and protocol manual.