Literature DB >> 3525681

Antinuclear antibody. Precise and accurate quantitation without serial dilution.

E Bonifacio, P N Hollingsworth, R L Dawkins.   

Abstract

A new method for measuring homogeneous pattern antinuclear antibody by immunofluorescence has been validated. This method exploits the differential sensitivity of rat heart muscle, kidney tubules and liver parenchyma as substrates for ANA, and employs calibrating sera. It provides quantitative measurement in the range 2.5-10 WHO IU/ml and semi-quantitative measurement up to 30 WHO IU/ml, without the need for serial dilution. The routine use of standards together with this method improves precision and provides conversion of measurements to IU/ml. These modifications make ANA a precise screening test for the exclusion of SLE.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 3525681     DOI: 10.1016/0022-1759(86)90486-2

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  3 in total

1.  Assessment of precision, concordance, specificity, and sensitivity of islet cell antibody measurement in 41 assays.

Authors:  E Bonifacio; C Boitard; H Gleichmann; M A Shattock; J L Molenaar; G F Bottazzo
Journal:  Diabetologia       Date:  1990-12       Impact factor: 10.122

2.  Precise quantitation of antinuclear antibodies on HEp-2 cells without the need for serial dilution.

Authors:  P N Hollingsworth; R I Dawkins; J B Peter
Journal:  Clin Diagn Lab Immunol       Date:  1996-07

3.  Standardisation of the quantitative determination of antinuclear antibodies (ANAs) with a homogeneous pattern.

Authors:  T E Feltkamp; F Klein; M B Janssens
Journal:  Ann Rheum Dis       Date:  1988-11       Impact factor: 19.103

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.