Description
8-
iso PGF
2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. It is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. The ratio of these two forms is approximately 2:1, with a total plasma 8-
iso PGF
2α level of about 150 pg/ml in normal volunteers. In normal human urine, 8-
iso PGF
2α levels are about 180-200 pg/mg of creatinine. 8-
iso PGF
2α is a weak TP receptor agonist in vascular smooth muscle. Conversely, 8-
iso PGF
2α inhibits platelet aggregation induced by U-
46619 (10
−6 M) and I-BOP (3 x 10
−7 M) with IC
50 values of 1.6 x 10
−6 M and 1.8 x 10
−6 M, respectively.
Description
8-
iso Prostaglandin F
2α (8-
iso PGF
2α) is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. It is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. The ratio of these two forms is approximately 2:1, with a total plasma 8-
iso PGF
2α level of about 150 pg/ml in normal volunteers. In normal human urine, 8-
iso PGF
2α levels are about 180-200 pg/mg of creatinine. 8-
iso PGF
2α is a weak TP receptor agonist in vascular smooth muscle. Conversely, 8-
iso PGF
2α inhibits platelet aggregation induced by U-
46619 (10
−6 M) and I-BOP (3 x 10
−7 M) with IC
50 values of 1.6 x 10
−6 M and 1.8 x 10
−6 M, respectively.
8-
iso Prostaglandin F
2α MaxSpec
® standard is a quantitative grade standard of 8-
iso Prostaglandin F
2α that has been prepared specifically for mass spectrometry and related applications where quantitative reproducibility is required. The solution has been prepared gravimetrically and is supplied in a deactivated glass ampule sealed under argon. The concentration was verified by comparison to an independently prepared calibration standard. This 8-
iso Prostaglandin F
2α MaxSpec
® standard is guaranteed to meet identity, purity, stability, and concentration specifications and is provided with a batch-specific certificate of analysis. Ongoing stability testing is performed to ensure the concentration remains accurate throughout the shelf life of the product.
Note: The amount of solution added to the vial is in excess of the listed amount. Therefore, it is necessary to accurately measure volumes for preparation of calibration standards. Follow recommended storage and handling conditions to maintain product quality.