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Rat GGT1/GGT ELISA Kit
  ANTIA80007-96
New Product
 :  
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Rat GGT1/GGT ELISA Kit
  ANTIA80007-96
New Product
 :  

 

  • Pk:
    96 Tests
  • Assay duration:
    Multiple steps
  • Assay Type:
    Sandwich
  • Format:
    Pre-coated
  • Host:
  • Primary antibody reactivity:
    Rat
  • Target protein:
    GGT1/GGT
  • Description:
    Rat GGT1/GGT ELISA kit
  • Environmentally Preferable:
  • Sample type:
    Serum, plasma, tissue homogenates and other biological fluids
  • Cross reactivity:
    Rat GGT1/GGT ELISA kit exhibits high specificity and excellent specificity for the detection of rat GGT1/GGT. No significant cross-reactivity or interference between GGT1/GGT 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:
    1,563 - 100 ng/ml
  • Storage temperature:
    4 °C
  • Sample volume:
    100 μl
  • Sensitivity:
    0,938 ng/ml
  • Regulatory status:
    RUO

 

 

Rat GGT1/GGT ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat GGT1/GGT in serum, plasma, tissue homogenates, and other biological fluids.

  • Ready-to-use ELISA Kit
  • Detection range: 1,563 to 100 ng/ml
  • Sensitivity: 0,938 ng/ml
  • Sample type: Serum, plasma, tissue homogenates, and other biological fluids
  • Assay precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%

Rat GGT1/GGT ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat GGT1/GGT in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for GGT1/GGT has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the GGT1/GGT 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-GGT1/GGT Antibody, which binds the captured GGT1/GGT 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 GGT1/GGT captured in each well. The concentration of GGT1/GGT 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.