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Free Estriol Saliva ELISA Kit

INTENDED USE

Human free estriol saliva ELISA kit is an accurate in vitro quantitative method for detecting free estriol (unconjugated estriol, E3, oestriol) in human saliva samples. This assay has a minimum sensitivity detection limit of 1.4 pg/ml.

BACKGROUND

Estriol (also known as oestriol and E3) is significantly produced in large amounts during pregnancy because of the fetus. It is regarded as of the one of the three main estrogens that are made by the human body and its production is dependent on an intact maternal-placental-fetal unit. The measurement of maternal concentration is useful in monitoring the fetal status during pregnancy especially in the third trimester.

DHEA-S is produced by the adrenal cortex of the fetus and this can be converted to estriol by the placenta. Fetal placental is responsible for producing estriol which results in a progressive increase in the maternal circulating levels that can reach a late gestational peak of many orders of magnitude greater than in non-pregnant levels.

CONTENT

All reagents supplied need to be stored at 2 °C – 8 °C, unopened reagents will retain reactivity until expiration date. Do not use reagents beyond this date.

  • Microtiterplate (96 wells): Coated with anti-estriol antibody.
  • Calibrators 0-5: Concentration 0, 2.5, 15, 100, 600, 4000 pg/ml.
  • Control 1 (Low) And Control 2 (High).
  • Enzyme Conjugate (100x): Consists of antibody conjugated to horseradish peroxidase (HRP).
  • Enzyme Conjugate Dilution Buffer.
  • Substrate Solution: Tetramethylbenzidine (TMB).
  • Stop Solution.
  • Wash Solution (10x Concentrated).

SENSITIVITY

The minimum sensitivity detection limit of free estriol (unconjugated estriol, E3, oestriol) using current estriol saliva ELISA kit was approximately 1.4 pg/ml. The dynamic range for this assay is 2.5 – 4,000.0 pg/ml.

ASSAY CHARACTERISTICS

– Analytical Sensitivity: 1.4 pg/ml
– Specificity (Cross Reactivity): Highly specific for estriol.
– Assay Dynamic Range: 0 – 4000 pg/ml.
– Intra-Assay Variation: 8.2 – 9.4%
– Inter-Assay Variation: 4.8 – 8.6%
– Recovery: 80 – 109%
– Interfering Substances: Blood contamination in saliva samples was found to affect the results, in this case blood is usually visible with the eye.

REFERENCES

  1. Enzyme immunoassay of unconjugated estriol in serum and saliva during pregnancy. Exp Clin Endocrinol. (1985) 86 (2): 178-84. Weissbach A., et al.
  2. ELISA for salivary and plasma estriol in pregnancy. Steroids. (1984) 43 (5): 469-79. Preti M.S., et al.
  3. The measurement of hormones in saliva: possibilities and pitfalls. J Steroid Biochem. (1987) 27 (1-3): 81-94. Review. Vining R.F. and McGinley R.A.
  4. Salivary unconjugated estriol levels in normal third trimester pregnancy – direct correlation with serum levels. Steroids. (1983) 41 (2): 145-53. Kundu N., et al.

ADDITIONAL INFORMATION

  • Full Name: Free Estriol Saliva ELISA Kit
  • Reactivity: Human
  • Sample Type: Saliva
  • Sensitivity: 1.4 pg/ml

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