PAPP-A, Mouse ELISAPAPP-A, Mouse ELISA
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PAPP-A, Mouse ELISA

The Mouse PAPP-A enzyme linked immunosorbent assay (ELISA) kit provides materials for the quantitative measurement of PAPP-A in mouse serum, cell supernatant, and other biological fluids.

Pregnancy-associated plasma protein-A (PAPP-A) is a novel zinc metalloproteinase that functions in many systems outside of pregnancy. PAPP-A expression has been reported in various tissues, including endometrium, testis, kidney, bone, colon, and other adult and fetal tissues.1-12 Abundant PAPP-A mRNA expression levels were found in visceral fat and these were 10-fold higher than in subcutaneous fat.10 PAPP-A expression significantly increases with age in kidney, brain and gonads10 and significantly deceases with age in bone and skeletal muscle.10 In the thymus, PAPP-A mRNA showed a biphasic response with age.10 Data in both humans and mice suggest a role for PAPP-A in aging and age-related diseases.10 Expression of IGFBP-5 mRNA, a marker of insulin-like growth factor-I (IGF-I) bioactivity known to be regulated by PAPP-A, paralleled the changes in PAPP-A expression with age in kidney, bone, skeletal muscle and thymus. PAPP-A is potentially proatherosclerotic and has been proposed as a new marker of inflammation, as high serum PAPP-A levels are observed in patients with renal impairment, asthma, lung cancer, etc.1-12 Stimulation of PAPP-A expression by intermittent PTH treatment contributes to PTH bone anabolism in mice.9 Effect of PAPP-A on tendon structure and mechanical properties have been studied8, However, quantitative determination of PAPP-A in mouse tissues with age are limited due to unavailability of the mouse PAPP-A ELISA.

References:
1. Bulut I, Coskun A, Ciftci A et al. Relationship between Pregnancy associated plasma protein A and lung cancer. The American Journal of the Medical sciences. April 2009; 337 (4): 241-244
2. Schindler AM, Bischof B. Histochemical localization of pregnancy associated plasma protein-A in fetal, infant, and adult organs and camparison between antisera. Gynecol Obstet Invest. 1984; 18: 88-94.
3. Overgaard MT, Oxvig C, Christiansen M , et al. Messenger ribonucleic acid levels of pregnancy-associated plasma protein-A and the preform of eosinophil major basic protein: expression in human reproductive and nonreproductive tissue. Biol Reprod 1999; 61:1083-1089.
4. Fialova L, Kalousova M, Soukupova J, et al. Relationship of pregnancy associated plasma protein A to renal function and dialysis modalities. Kidney Blood Press Res. 2004; 27: 88-95.
5. Coskun A, Balbay O, Duran S et al. Pregnancy-associated plasma protein A and asthama. Adv Ther. 2007; 24: 362-367.
6. Coskun A, Duran S, Apaydin S, et al. Pregnancy-associated plasma protein A: evaluation of a new biomarker in renal transplanted patients. Transplant Proc. 2007; 39:3072-3076.
7. Bayes-Genis A, Conover CA, Overgaard MT, et al. Pregnancy-associated plasma protein A as a marker of acute coronary syndromes. N Engl J Med. 2001; 345: 1022-1029.
8. Yang TH, et al. PAPP-A affects tendon structure and mechanical properties. J Struct Biol. Oct 2015; 192(1):59-66.
9. Clifton KB, et al. Pregnancy-associated plasma protein-A modulates the anabolic effects of parathyroid hormone in mouse bone. Bone. Dec 2015; 81:413-6.
10. Harstad SL, et al. Tissue-specific changes in pregnancy associated plasma protein-A expression with age in mice. Endocrinology. Sep 2014; 57:13-7.
11. Bale LK, et al. Inducible reduction in pregnancy-associated plasma protein-A gene expression inhibits established atherosclerotic plaque progression in mice. Endocrinology, Apr 2014; 155(4):1184-7.
12. Conover CA, et al. Preferential impact of pregnancy-associated plasma protein-A deficiency on visceral fat in mice on high-fat diet. Am J Physiol Endocrinol Metab. Nov 2013; 305(9):E1145-53.
13. HHS Publication, 5th ed., 2007. Biosafety in Microbiological and Biomedical Laboratories. Available http://www.cdc.gov/biosafety/publications/bmbl5/BMBL5
14. DHHS (NIOSH) Publication No. 78€“127, August 1976. Current Intelligence Bulletin 13 - Explosive Azide Hazard. Available http:// www.cdc.gov/niosh.
15. Approved Guideline €“ Procedures for the Handling and Processing of Blood Specimens, H18-A3. 2004. Clinical and Laboratory Standards Institute.
16. Kricka L. Interferences in immunoassays €“ still a threat. Clin Chem 2000; 46: 1037€“1038.

Cat# Size Price Qty Buy
AL-158 96 Well Plate £720.00

Additional Information

Property Value or Rating
Product Size 96 Well Plate
Manufacturer Ansh Labs
Analyte PAPP-A
Assay Time 3.5 hours
Detection HRP-based ELISA, colorimetric detection by dual wavelength absorbance at 450 nm and 630 nm as reference filter
Dynamic Range 6, 0.24-10.3 ng/mL
Detection Limit 0.020 ng/mL
Product Line Immunoassay
Special Notes For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Sample Size 25 µL
Samples Plasma,Serum
Shelf Life 24 months
Reactivity Bovine, Canine, Caprine, Equine, Mouse, Ovine, Rabbit

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