ABSTRACT
OBJECTIVES@#To study the changes of protein levels in peripheral blood after it dried.@*METHODS@#The proteins from whole blood and bloodstains were detected by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and normalized by the label-free quantification (LFQ) method. The differential proteins were analyzed by using R 4.2.1 software, limma and edgeR package. The analysis of biological function, signaling pathway and subcellular localization for the differential proteins was then performed.@*RESULTS@#A total of 623 and 596 proteins were detected in whole blood and bloodstains, respectively, of which 31 were statistically significant in the quantitative results, including 10 up-regulated and 21 down-regulated proteins in bloodstains.@*CONCLUSIONS@#The protein abundances in whole blood and bloodstains are highly correlated, and the variation of protein abundances may be related to the changes of endogenous and structural proteins in cells. The application of proteomics technology can assist the screening and identification of protein biomarkers, thereby introducing new biomarkers for forensic research.
Subject(s)
Chromatography, Liquid/methods , Tandem Mass Spectrometry/methods , Proteomics/methods , Blood Stains , BiomarkersABSTRACT
The distribution of C_3 phenotype frequencies in the Han population in Cheng-du area was studied by means of cellulose acetate electrophoresis followed byimmunofixation.In 400 unrelated healthy individuals three C_3 phenotypes weredemonstrated.Their frequencies were as follows:SS=397,FS=2 and SSvar=1.Their gene frequencies were as follows:C_3~S=0.9963,C_3~F=0.0025 and C_3~(svar)=0.0013.The C_3 phenotype frequencies were in good agreement with those expec-ted.C_3 phenotyping in the huma bloodstains kept at 37℃ and room temp-lasserature for two days,at 4℃ for 23 days(cotton bloodstains)and for 35 days(g-bloodstains),and -20℃ for at least 87 days could be performed.C_3 ph-enotypingin human serum could be performed at roon temperature for 3 days,as 4℃ for 13days and at -20℃ for at least 106 days.C_3 phenotyping was usedin five casesof paternity dispute.
ABSTRACT
A PAGE IEF immunoassay was established to detect the ORM, Pi, AHSG and GC phenotypes slmultaneously in human bloodstains. The cumulative discriminating power and probability of paternity exclusion were 0. 9878 and 0. 6648 respectively. Human sera diluted 100 times and bloodstains kept at room temperature for 4 weeks could be typed for these four blood groups correctly. The phenotypes of ORM, AHSG and GC could be determined correctly in bloodstains kept at room temperature within 24 weeks. This provides a good approach for individual identification of human bloodstains.
ABSTRACT
The polymorphism of Bf was determinated in 234 healthy human sera in Beijing by agarose gel high-voltage electrophoresis and PAGIEF followed by immunofixation. The distribution of Bf phenotypes was observed: SS 171, FS 49, FF 8, SS07 4, FS07 1 and SS045 1. Their allele frequencies were, Bf~s = 0.8462, Bf~F=0.1410, Bf~(S07)=0.0107, Bf~(S045)=0.0021. The distribution of Bf phenotypes was good agreement with the Hardy-weinberg law.The time limits of Bf phenotypes in 22 bloodstain samples was determinated.
ABSTRACT
The phenotyping of erythrocyte esterase D of 221 Chinese random donors,Han nationalities in Shenyang,China,was performed by the agarose gel electrophoresis.Gene frequencies were:E_SD~1=0.629,E_SD~2= 0.371.There is no significant difference of gene frequencies of Han nationalities between Shenyang and Beijing.The minimal amount meeted the requirment for detection of E_S D were 1?l of fresh hemolysate or 1?l hemolysate.The E_S D can be detected from the hemolysates kept in 37℃ for 7～8days as well as from 1?l hemolysate bloodstain kept for 2 weeks and 5?l hemolysate bloodstain kept for 3 weeks.