1987
DOI: 10.1111/j.1471-4159.1987.tb13122.x
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Human γγ‐Enolase: Two‐Site Immunoradiometric Assay with a Single Monoclonal Antibody

Abstract: A monoclonal antibody (mAb), termed BBS/NC/VI-H14 (H14), that reacts with the human enzyme gamma gamma-enolase was prepared. It was directed against the gamma-subunit and did not cross-react with the alpha- or beta-subunit. The mAb H14 can be used for quantitative determination of gamma gamma-enolase in a two-site immunoradiometric assay (two-site IRMA). It is also suitable for immunostaining formalin-fixed tissues. The specific identification of gamma gamma-enolase provided by the two-site IRMA with H14 is di… Show more

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Cited by 24 publications
(9 citation statements)
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“…Specimens were fixed in formalin and were processed routinely, with 4-m sections being stained with hematoxylin and eosin and PAM. The avidin-biotin complex (ABC) immunoperoxidase method was also used in conjunction with the following antibodies: proliferating cell nuclear antigen (PCNA) for staining cells in the S-phase of the cell cycle (DAKO, Glostrupp, Denmark) [11], S-100 for human S-100 A and B (DAKO) [12], NSE to identify cells of neurogenic origin (DAKO) [13], and ␣SMA for smooth muscles (DAKO) [14]. Normal skin from the surgical operation material was used as control.…”
Section: Hair Removal Proceduresmentioning
confidence: 99%
“…Specimens were fixed in formalin and were processed routinely, with 4-m sections being stained with hematoxylin and eosin and PAM. The avidin-biotin complex (ABC) immunoperoxidase method was also used in conjunction with the following antibodies: proliferating cell nuclear antigen (PCNA) for staining cells in the S-phase of the cell cycle (DAKO, Glostrupp, Denmark) [11], S-100 for human S-100 A and B (DAKO) [12], NSE to identify cells of neurogenic origin (DAKO) [13], and ␣SMA for smooth muscles (DAKO) [14]. Normal skin from the surgical operation material was used as control.…”
Section: Hair Removal Proceduresmentioning
confidence: 99%
“…They did not increase in any particular neu rological disease. In 3 cases of AD the results were within the normal range [Soler Federsppiel et al, 1987], (5) Neurofilament proteins were deter mined in 50 CSF samples. Normal values seem to be lower than 3.5 ng/ml.…”
Section: Resultsmentioning
confidence: 99%
“…The determinations of SI00 , MBP , yy-enolase [Soler Federsppiel et al, 1987] did not yield complementary diagnostic informa tion. Neurofilament proteins were increased in CSF of different neurological diseases and of 2 cases of familial AD.…”
Section: Discussionmentioning
confidence: 99%
“…We used enolase 2 (NSE, gamma neuronal), also known as ENO2. This isoenzyme is a homodimer found in mature neurons and cells of neuronal origin 8. Sixty formalin-fixed and paraffin-embedded tissue sections with the most representative hot spot triangular chiral mirror geometry complex areas were analyzed using neuron-specific enolase antibody marker.…”
Section: Neuron-specific Enolase Immunostainmentioning
confidence: 99%