Human acute phase Serum Amyloid A protein, SAA, as inflammatory marker
Human SAA ELISA for detection in urine, plasma and serum
Human SAA and inflammation
- Serum amyloid A (SAA) is predominantly produced by the liver
- Extra-hepatic production by macrophages, endothelial cells, epithelial cells, artherosclerotic lesions, tumors and synovial tissue
- Four different genes in human produce SAA. SAA-1 is the predominant form in plasma
- SAA is a major acute phase protein
- Belongs to family of pentraxins (i.e. PTX3, CRP)
- SAA functions as chemo-attractant
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Human SAA detection in urine
- To exclude matrix influence, urine with low SAA (#3) and urine with higher SAA (#4) concentration were mixed in different ratios
- The calculated concentration of human SAA was plotted versus the expected concentration of human SAA (Fig 1)

Evaluation of matrix-influence
- To exclude matrix influence, several serum and urine samples were diluted and recovery was calculated (Fig 2)
- Minimal dilutions of 5x and 50x are recommended for urine and serum, respectively

Human SAA and disease
- SAA is an early indicator for transplant rejection
- Increase in human SAA within hours after bacterial as well as viral infection
- Predictor for coronary artery disease in women
- SAA functions in various physiological and pathological processes
- SAA is linked to inflammation, atherosclerosis, thrombosis, AA-amyloidosis, rheumatoid arthritis, and neoplasia.
- Sensitive marker of acute inflammatory state

Hallmarks of human SAA ELISA (Cat# HK333)
- Unique assay for measurement in urine
- Human SAA concentration rises earlier and sharper than acute phase protein CRP
- Human SAA is increased after bacterial as well as viral infection
- Benchtop stability of standard > 95% (2 hrs RT; o/n 4 °C)
- Working time of 2.5 hours
- 100 µl sample/well
- Detection limit 3.1 ng/ml
- Useful for serum, plasma, fat-biopts and urine
- Detection of natural SAA-1
- Normal values in serum and plasma range from 1-5 µg/ml
- Acute inflammation may results in 1000-fold increase in human SAA
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