8 isoprostane ELISA Kit (ab175819)
Key features and details
- Sensitivity: 1 pg/ml
- Range: 0.005 ng/ml - 5 ng/ml
- Sample type: Cell culture extracts, Plasma, Serum, Tissue, Urine
- Detection method: Colorimetric
- Assay type: Competitive
Overview
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Product name
8 isoprostane ELISA Kit -
Detection method
Colorimetric -
Precision
Intra-assay Sample n Mean SD CV% Overall 12 0.43% Inter-assay Sample n Mean SD CV% Overall 12 1.75% -
Sample type
Urine, Serum, Plasma, Cell culture extracts, Tissue -
Assay type
Competitive -
Sensitivity
1 pg/ml -
Range
0.005 ng/ml - 5 ng/ml -
Assay duration
Multiple steps standard assay -
Product overview
Abcam’s 8 isoprostane competitive in vitro ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the determination of 8 isoprostane levels in biological samples. The isoprostanes are a family of eicosanoids of non-enzymatic origin produced by the random oxidation of tissues phospholipids by oxygen radicals. A recent NIH-sponsored study on Biomarkers of Oxidative Stress has indicated that 8 isoprostane is the best index of oxidative injury in a well-accepted oxidant stress rat model. In addition, plasma 8 isoprostane levels were found to be elevated in elderly subjects with severe hypertension and in urine from subjects with high fat diet-induced liver steatosis.
This kit can be used for the determination of 8 isoprostane in diluted urine, serum, plasma, cells and tissues following proper isolation and purification of the eicosanoid from the isoprostane-containing sample.
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Platform
Microplate
Properties
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Storage instructions
Store at -20°C. Please refer to protocols. -
Components 1 x 96 tests 1,000X 8-isoprostane HRP Conjugates 1 x 12µl 8-isoprotane Standard 1 x 2µl HRP Buffer 1 x 15ml Pre-coated 96-Well Microplate 1 unit 10X Sample Dilution Buffer 1 x 25ml TMB Substrate 1 x 24ml 10X Wash Buffer Solution 1 x 25ml -
Research areas
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Alternative names
- Prostaglandin, iso Prostaglandin F2, iso Prostaglandin, iPF2 alpha
Images
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Typical Standard Curve
Example of standard curve obtained with ab175819.
