Medical Technologies

Reagent Set for Quantitative Determination of 17α-Hydroxyprogesterone in Human Serum or Plasma Using Immunoenzymatic Analysis "IFА-17-ОН-ПГ" According to TU 9398-018-17253567-2006

Reagent Set for Quantitative Determination of 17α-Hydroxyprogesterone in Human Serum or Plasma Using Immunoenzymatic Analysis "IFА-17-ОН-ПГ" According to TU 9398-018-17253567-2006

The "IFА-17-ОН-ПГ" reagent set is designed for the quantitative determination of 17α-hydroxyprogesterone in human serum or plasma using immunoenzymatic analysis (ELISA), in accordance with TU 9398-018-17253567-2006.

Reagent Set Components:

  • 96-Well Plate: Polystyrene, with immobilized mouse monoclonal IgG antibodies to 17α-OH-PG human on the inner surface of the wells – 1 unit.
  • Calibration Samples: Human serum-based samples containing known amounts of 17α-OH-PG, as follows:
    • 0 ng/mL (1.0 ml)
    • 0.2 ng/mL (0.8 ml)
    • 0.4 ng/mL (0.8 ml)
    • 1.6 ng/mL (0.8 ml)
    • 6.4 ng/mL (0.8 ml)
    • 19.2 ng/mL (0.8 ml)
  • Conjugate: 17α-OH-PG conjugated with horseradish peroxidase – 1 vial (6.0 ml).
  • TMБ Solution: 11x concentrated – 1 tube (1.5 ml).
  • Control Serum: Human serum with a known content of 17α-OH-PG – 1 tube (0.6 ml).
  • Wash Solution: 20x concentrated – 1 bottle (50 ml).
  • Substrate Buffer: 1 bottle (15 ml).
  • Stop Reagent: 1 bottle (15 ml).

Choose the "IFА-17-ОН-ПГ" reagent set for precise and quantitative determination of 17α-hydroxyprogesterone in human biological samples.


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The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.

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