A Monoclonal Antibody Applicable for Determination of C-Peptide of Human Proinsulin by RIA

Hybridoma ◽  
1991 ◽  
Vol 10 (3) ◽  
pp. 379-386 ◽  
Author(s):  
I. HILGERT ◽  
P. ŠTOLBA ◽  
H. KRIŠTOFOVÁ ◽  
I. ŠTEFANOV ◽  
B. BENDLOVÁ ◽  
...  
1992 ◽  
Vol 38 (2) ◽  
pp. 227-232 ◽  
Author(s):  
F J Dhahir ◽  
D B Cook ◽  
C H Self

Abstract We describe an amplified enzyme-linked immunoassay of human proinsulin in serum that detects intact proinsulin and both the 32/33 and 65/66 split forms. The method uses the IgG fraction of a polyclonal antibody raised in a guinea pig against intact proinsulin, which we used to coat plastic microtiter plates. A sandwich was formed with proinsulin by using a monoclonal antibody against C-peptide labeled with alkaline phosphatase. We quantified the reaction by using the enzyme amplification procedure, which detected as little intact proinsulin as 0.1 pmol/L. We found no cross-reactivity with C-peptide in the assay, and decreased recovery attributable to the presence of insulin could be demonstrated only with a 30-fold excess of this hormone over proinsulin.


Author(s):  
HJM Van Rijn ◽  
JBL Hoekstra ◽  
JHH Thijssen

Three commercially available methods for the determination of C-peptide in human serum were evaluated. All kits were found to be acceptable with respect to precision and analytical recovery, while differences were observed with respect to sensitivity and cross-reactivity to human proinsulin. Furthermore an intermethod comparison was performed. It is pointed out that, before C-peptide determination on serum from insulin-treated diabetic subjects, a PEG precipitation, to remove antibody-bound proinsulin, should be done.


2011 ◽  
Vol 6 (1) ◽  
pp. 115
Author(s):  
A. Sanz-Paris ◽  
A. Rodriguez-Valle ◽  
D. Boj ◽  
J.L. Gascon ◽  
T. Corrales ◽  
...  

2000 ◽  
Vol 14 (3) ◽  
pp. 85-92 ◽  
Author(s):  
Li-Jiang Xuan ◽  
Hiroyuki Tanaka ◽  
Satoshi Morimoto ◽  
Yukihiro Shoyama ◽  
Hiroshi Akanuma ◽  
...  

In order to prepare the monoclonal antibody against 1,5-anhydro-glucitol (1), it was conjugated with bovine serum albumin (BSA), human serum albumin (HSA) or chicken lysozyme (CL) using succinate orβ-alanine succinate as a spacer to produce individual antigen conjugates. The number of hapten contained in each antigen conjugate was determined by matrix-assisted laser desorption/ionization tof mass (MALDI-tof-MS) spectrometry. The formation of monoclonal antibody (MAb) was also discussed.


2014 ◽  
Vol 289 (23) ◽  
pp. 16478-16486 ◽  
Author(s):  
Motohiro Nonaka ◽  
Michiko N. Fukuda ◽  
Chao Gao ◽  
Zhen Li ◽  
Hongtao Zhang ◽  
...  

1986 ◽  
Vol 59 (8) ◽  
pp. 2445-2449 ◽  
Author(s):  
Mitsuaki Narita ◽  
Toshihiko Ogura ◽  
Kazuhiro Sato ◽  
Shinya Honda

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