Document Detail


Analysis of the genetic polymorphism of coagulation factor XIIIB (FXIIIB) by isoelectric focusing.
MedLine Citation:
PMID:  3234386     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The genetic variants of the coagulation factor XIIIB (FXIIIB) were analyzed by isoelectric focusing, carried out in agarose gels and followed by immunofixation. The FXIIIB phenotypes were visualized by a combined staining procedure with Coomassie Brilliant Blue R-250 and silver nitrate. Improved resolution was accomplished in polyacrylamide gels by hybrid isoelectric focusing in immobilized pH gradients supplemented with carrier ampholytes. We examined a total of 1,604 unrelated, healthy individuals from Southern Germany. The frequencies for the FXIIIB alleles were B*1 = 0.7581, B*2 = 0.0843, B*3 = 0.1568 and B*4 = 0.0019. The theoretical exclusion rate for disputed paternity is 22.35%.
Authors:
H J Leifheit; H Cleve
Related Documents :
22645096 - The evolutionary history of the white-rayed species of melampodium (asteraceae) involve...
22834676 - Karyotype variation is indicative of subgenomic and ecotypic differentiation in switchg...
2848756 - Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of...
15497446 - Cloning and characterization of a splice variant of human bardet-biedl syndrome 4 gene ...
17492756 - Chromosomal imbalances are associated with outcome of helicobacter pylori eradication i...
16816916 - Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Electrophoresis     Volume:  9     ISSN:  0173-0835     ISO Abbreviation:  Electrophoresis     Publication Date:  1988 Aug 
Date Detail:
Created Date:  1989-05-10     Completed Date:  1989-05-10     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8204476     Medline TA:  Electrophoresis     Country:  GERMANY, EAST    
Other Details:
Languages:  eng     Pagination:  426-9     Citation Subset:  IM    
Affiliation:
Blood Transfusion Service, Bavarian Red Cross, Munich, Federal Republic of Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Ampholyte Mixtures
Factor XIII / analysis,  genetics*
Humans
Isoelectric Focusing
Phenotype
Polymorphism, Genetic*
Chemical
Reg. No./Substance:
0/Ampholyte Mixtures; 9013-56-3/Factor XIII; 97089-56-0/factor XIIIb

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Application of plasminogen polymorphism to forensic hemogenetics.
Next Document:  Two new esterase D (ESD) variants revealed by isoelectric focusing in agarose gel.