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Cyclophilin A Human ELISA

  • Regulatory status:RUO
  • Type:Sandwich ELISA, Biotin-labelled antibody
  • Other names:Peptidyl-prolyl cis-trans isomerase A, PPIase A, Cyclosporin A-binding protein, Rotamase A, PPIA, CYPA
  • Species:Human
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Cat. No. Size Price


RD191329200R 96 wells (1 kit)
PubMed Product Details
Technical Data

Type

Sandwich ELISA, Biotin-labelled antibody

Applications

Serum, Plasma-EDTA, Plasma-Heparin, Plasma-Citrate

Sample Requirements

35 µl

Storage/Expiration

Store the complete kit at 2 8°C. Under these conditions, the kit is stable until the expiration date (see label on the box)

Calibration Curve

Calibration Range

0.39 – 25 ng/ml

Limit of Detection

0.28 ng/ml

Intra-assay (Within-Run)

n = 8; CV = 3.1 %

Inter-assay (Run-to-Run)

n = 6; CV = 4.2 %

Spiking Recovery

94.9 %

Dilutation Linearity

95.5 %

Summary

Features

  • It is intended for research use only
  • The total assay time is less than 3.5 hours
  • The kit measures CYPA in serum and plasma (EDTA, citrate, heparin)
  • Assay format is 96 wells
  • Standard is recombinant protein based
  • Components of the kit are provided ready to use, concentrated or lyophilized

Research topic

Cardiovascular disease, Immune Response, Infection and Inflammation, Oncology

Summary

Cyclophilins belong to a group of proteins that have peptidyl-prolyl cis-trans isomerase activity; such proteins are collectively known as immunophilins and also include the FK-506-binding proteins and the parvulins. Cyclophilins are found in all cells of all organisms studied, in both prokaryotes and eukaryotes. Human have a total of 16 cyclophilin proteins. Cyclophilins also have varying degrees of affinity for the immunosuppressive drug Cyclosporine A (CsA), a cyclic 11-amino-acid peptide produced by fungus Tolypocladium infantum. Cyclophilin A, in particular, is the major intracellular receptor for CsA. Cyclophilin A (CYPA) is the first member of the cyclophilins to be identified in mammals. Human genes of CYPA, also known as Cyp18, are located on chromosome 7p11.2-p13 and encode the protein, which consists of 165 amino acid residues with a relative molecular mass approximately 18 kDa. Human CYPA has an eight-stranded antiparallel β-barrel structure, with two α-helices enclosing the barrel from either side. Seven aromatic and other hydrophobic residues form a compact hydrophobic core within the barrel, usually in the area where CsA binds. A loop from Lys118 ti His126 and four β-strands (β3-β6) make up the binding site for CsA. In mammals, the CsA-CYPA complex binds to and inhibits calcineurin, a calcium-calmodulin-activated serine/threonine-specific protein phosphatase. The inhibition of calcineurin blocks the translocation of nuclear factor of activated T cells from the cytosol to the nucleus, thus preventing the transcription of genes encoding cytokines such as interleukin-2. Extracellular CYPA has a potent chemotactic effect on leukocytes, monocytes, and lymphocytes. CYPA is believed to be a key molecule in many biological functions including molecular chaperoning, protein folding, protein trafficking, immune modulation and cell signaling. Secreted CYPA activates cardiovascular cells resulting in a variety of cardiovascular diseases, including vascular remodeling, abdominal aortic aneurysms formation, atherosclerosis, cardiac hypertrophy and myocardial ischemic reperfusion injury. Intracellular CYPA is secreted from cells in response to inflammatory stimuli such as hypoxia, infection and oxidative stress. Its expression increases in inflammatory conditions including rheumatoid arthritis, autoimmune disease and cancer. CYPA levels are higher in the serum and synovial fluids of rheumatoid arthritis patients and are also elevated in tumors including non-small cell lung cancer, pancreatic adenocarcinoma, hepatocellular carcinoma, oral cancer, buccal squamous cell carcinomas and breast cancer.

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