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Rat CXCR2 ELISA Kit
Rat CXCR2 ELISA Kit
  76737-174
 :  
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Rat CXCR2 ELISA Kit
  76737-174
 :  A87332-96
 :  

 

  • Assay duration:
    Multiple steps
  • Assay Type (ELISA with LOV):
    Sandwich
  • Format:
    Pre-coated
  • Primary antibody reactivity:
    Rat
  • Target protein:
    CXCR2
  • Description:
    Rat CXCR2 ELISA kit
  • Size:
    96 tests
  • Sample Type:
    Serum, plasma, tissue homogenates and other biological fluids
  • Cross Reactivity:
    Rat CXCR2 ELISA kit exhibits high specificity and excellent specificity for the detection of rat CXCR2. No significant cross-reactivity or interference between CXCR2 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:
    46.875 - 3000 pg/ml
  • Storage Temperature:
    4 °C
  • Sample Volume:
    100 μl
  • Sensitivity:
    28.125 pg/ml
  • Regulatory Status:
    RUO
  • Cat. No.:
    76737-174

 

 

Rat CXCR2 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat CXCR2 in serum, plasma, tissue homogenates, and other biological fluids.

  • Ready-To-Use ELISA Kit
  • Detection Range: 46.875 - 3000 pg/ml
  • Sensitivity: 28.125 pg/ml
  • Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
  • Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%

Rat CXCR2 ELISA kit (A87332) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat CXCR2 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for CXCR2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CXCR2 present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-CXCR2 Antibody, which binds the captured CXCR2 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 visualize 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 CXCR2 captured in each well. The concentration of CXCR2 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, lyophilized 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.