CNP Antibody RIA
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C-Type Natriuretic Peptide (CNP) Antibody and RIA Kit

 
Presence and distribution of CNP immunoreactivity in renal tissue of normal subjects and nephrotic patients. A: negative control with normal goat serum in normal kidney. B: CNP in distal tubules of normal kidney. C: CNP in proximal collecting tubules and in the visceral and parietal layer of glomerular tissue of normal kidney. D: negative control with normal goat serum in nephrotic kidney. E: CNP in distal tubules of nephrotic kidney. F: CNP in proximal collecting tubules and in the visceral and parietal layer of the glomerular tissue in nephrotic kidney.
Endocrine Reviews 27 (1): 47-72
Radioimmunoassay for plasma C-type natriuretic peptide determination: a methodological evaluation.

PATHOPHYSIOLOGY, TECHNOLOGY ASSESSMENT AND OUTCOME STUDY

Clinical Chemistry & Laboratory Medicine. 43(6):641-645, June 2005.
Del Ry, Silvia; Maltinti, Maristella; Emdin, Michele; Passino, Claudio; Catapano, Giosue; Giannessi, Daniela *

Abstract:
C-Type natriuretic peptide (CNP) is a member of the family of natriuretic peptides with vasodilatory properties, and is produced and secreted by endothelial cells. It seems to play a central role in the paracrine vasomotor control of tone and to be important in several clinical conditions characterized by endothelial dysfunction. We evaluated the analytical performance of a commercially available radioimmunoassay for CNP (CNP-22 (HUman, Rat, Mouse) RIA Kit, Phoenix Pharmaceuticals, Inc.) after a preliminary extraction with Sep-Pak C18. Its analytical reliability was checked by determination of CNP plasma levels in healthy subjects (n=23) and in patients with different diseases, likely characterized by endothelial dysfunction, such as chronic heart failure (n=133) and cirrhosis (n s 84). The extraction yield was 78+/-3%. Accuracy of the radiommunological determination was evaluated by dilution (45-370 [mu]L of extracted plasma) and recovery tests (>80%). Between- and within-assay variabilities were <=10% and analytical sensitivity was 0.41+/-0.015 pg/tube. Plasma CNP in patients with chronic heart failure and with cirrhosis was significantly raised compared to controls (p<0.0001 and p=0.001, respectively). The sensitivity, accuracy and variability levels of the method proposed for CNP assay was suitable for reliable detection of changes in CNP plasma levels in the clinical setting.

A: plasma CNP concentration in control subjects and nephrotic syndrome (NS) patients on normal protein diet (NS+NPD) and on low protein diet (NS+LPD). B: urinary CNP excretion, evaluated as CNP-to-creatinine (Cr) ratio, in control subjects, NS+NPD, and NS+LPD. Values are means ± SE. * P < 0.05 vs. controls; #P < 0.05 vs. NS. (CNP-22 RIA Kit from Phoenix Pharmaceuticals) Am J Physiol Renal Physiol 283: F464-F472, 2002
Individual changes in urinary CNP excretion (µg/g of creatinine; A), urinary guanosine 3',5'-cyclic monophosphate (cGMP) excretion (µg/g of creatinine; B), proteinuria (g/g of creatinine; C), and albuminuria (g/g of creatinine; D) after an LPD. Am J Physiol Renal Physiol 283: F464-F472, 2002
 
 
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Quantity
Price ($)
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CNP-53 (1-29) (P, R) Antibody Purified IgG, FITC Labeled FG-G-012-06B
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CNP-53 (1-29) (P, R) Antibody Purified IgG, Rhodamine Labeled FR-G-012-06
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CNP-53 (1-29) (P, R) Antibody Purified IgG, Cy3 Labeled FC3-G-012-06
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CNP-53 (1-29) (P, R) 012-06
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CNP-22 (Human, Rat, Mouse) RIA Kit RK-012-03
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CNP-22 (Human, Rat, Mouse) Antibody H-012-03
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CNP-22 (Human, Rat, Mouse) EIA Kit EK-012-03
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