Determination of the Lewis blood group substances in stains of forensically relevant body fluids

1986 ◽  
Vol 30 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Gerhard Bässler
Vox Sanguinis ◽  
1962 ◽  
Vol 7 (3) ◽  
pp. 329-333 ◽  
Author(s):  
T. W. Lodge ◽  
A. Usher

1986 ◽  
Vol 26 (2) ◽  
pp. 103-106 ◽  
Author(s):  
Anne Davies

This paper is based on a lecture given to an audience consisting mainly of social workers and paediatricians. The purpose of the talk was to explain the sort of evidence that could be provided by a forensic biologist in order to show that a child had been sexually assaulted, and to help identify the assailant. The introduction to the talk was composed of a review of the types of cases involving the sexual abuse of children that have been dealt with by this laboratory during the last two years (1984–85). A description was then given of the various biological materials which, if found in appropriate places, can substantiate an allegation of sexual assault. A brief reference was made to the persistence of semen in the vagina, rectum and mouth, and to the blood group substances which occur in different body fluids.


Vox Sanguinis ◽  
1962 ◽  
Vol 7 (3) ◽  
pp. 329-333
Author(s):  
T.W. Lodge ◽  
A. Usher

2019 ◽  
Vol 2 (1) ◽  
pp. 31-38
Author(s):  
Abdul Halim Sadikin ◽  
Yefta Moenadjat ◽  
Novi Sylvia Hardiany

Background: Usually it takes a large number of volume sample to determine blood group from external secretion fluids. But, in certain condition, samples are only available in very small amount. The objective of this study is to detect the presence of ABO blood group substances in mucosal fluid using ELISA technique, thus only requires small amount of samples.Objective: To develop an ELISA technique using the current anti-ABO antibodies for determination of blood group by hemagglutination technique and second peroxidase label antibody specific for mouse IgG, originally used for another ELISA technique.Methods: 100 μl of diluted human intestinal mucosal fluid were incubated overnight in 4oC in ELISA microplate wells, followed by addition anti-ABO antibodies. Then after incubation, a second revealing antibody anti mouse IgG labeled with peroxidase was added. After a brief incubation, substrate H2O2 and chromogenic TMB were added.Results: Positive reaction is marked by development of blue colour, which, on termination enzymatic reaction by addition 100 μl H2SO4 change to yellow.Conclusion: An ELISA method for detecting ABO substance in mucosal fluid can be developed from antibodies not specifically made for this technique, but specific only for the target.


Author(s):  
Ravindra Pal Verma ◽  
Arun Kumar ◽  
Dr. Harsh Sharma

Urine samples collected from 20 donors with unknown blood group and secretor status had been determined from saliva. ABO typing on the concentrated samples was successfully performed after 1 month of storage. Urine stained clothing samples are often submitted to forensic science laboratories for ABH blood group antigen determination. The serogenetic markers of urine stains submitted can be used to determine the origin of any of these samples. ABH blood group substances have previously been identified from urine. ABH blood group substance is low in urine in comparison with other body fluids


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