Haptoglobin phenotyping of bloodstains by horizontal electrophoresis on a compact polyacrylamide gradient gel

A method is described for phenotyping haptoglobin by horizontal electrophoresis on a small polyacrylamide gradient gel. This method employs the same apparatus used in the separation of many red cell enzyme phenotypes and thereby eliminates the necessity for specialized vertical electrophoresis equipment.     

Gm(11) grouping of dried bloodstains

An absorption inhibition method for the detection of gamma marker Gm(11) in dried bloodstains is described. Particular reference is made to the association of Gm(11) with Gm(-1, -2). When a dried bloodstain fails to inhibit anti-Gm(1) and anti-Gm(2), this may represent a true Gm(-1, -2) result or there may be insufficient material to inhibit either antibody. The detection of Gm(11) in a bloodstain extract provides an objective means of confirming the apparent absence of Gm(1) and Gm(2) as representing a true Gm(-1, -2) result. This antigen compares very well with other blood group systems with regard to the amount of bloodstain required for analysis and its stability. No evidence is available for preferential loss of Gm(1) and Gm(2) relative to Gm(11) in dried bloodstains.     

Determination of alpha1-fetoprotein in bloodstains by means of electrophoresis on cellulose acete (author's transl)]

The distinction of foetal from adult blood stains prepared from 219 cord blood samples was possible, without exception, up to eight months by means of alpha1-fetoprotein precipitation, carried out by immuno-electrophoresis on cellulose acetate (Biotest) instead of agar gel, as described by Patzelt, Geserick and Lignitz. The material carrying the blood stains (glass, wood, paper and linen) did not influence the results.     

Phosphoglucomutase (PGM) grouping of bloodstains on silver.

This paper describes a case involving alteration of phosphoglucomutase (PGM) isoenzyme patterns in bloodstains present on silver. The effect could be produced by treating blood samples with silver nitrate solution.     

Detectability of group-specific component (Gc) in aged bloodstains

An improved method of group-specific component (Gc) typing was conducted electrophoretically on agarose gel. Individual bloodstains randomly collected from different individual donors over a five-year period at intervals of approximately one month were checked for Gc activity. Group-specific component was typed accurately in dried bloodstains stored at room temperature up to 43 months in age. From 100 different donors, bloodstains ranging in age from 38 to 43 months were tested by the methods described and 73% of the samples were interpretable for Gc.     

Immunofixation of complement component C3 phenotypes in bloodstains after cellulose acetate electrophoresis

The determination of the polymorphic C3 phenotypes was accomplished by electrophoresis on cellulose acetate followed by immunofixation. The three common phenotypes resulting from the two common codominant alleles C3S and C3F were clearly distinguishable in blood and bloodstain samples. Storage and degradation of C3 in blood samples as well as the stability of C3 in dried bloodstains is discussed.     

Lewis typing of human bloodstains by enzyme-linked immunosorbent assay (ELISA) using monoclonal anti-Le(a) and anti-Le(b)

The Lewis blood grouping of human dried bloodstains could be determined by an enzyme-linked immunosorbent assay (ELISA) using monoclonal anti-Le(a) and anti-Le(b) antibodies with an avidin-biotin complex (ABC). The bloodstains aged 1 year were used as samples, and approximately 1 mg of the stains was enough to type each Lewis antigen reliably by this method. The Lewis substances of 106 individual stains were correctly typed regardless of their ABO blood group system.     

紫外可见漫反射光谱法无损确证血痕的研究

目的建立一种快速确定血痕的方法。方法将人血、猪血、鸡血、羊血等制成样品纱布,利用紫外可见分光光度计扫描反射光谱进行检测,同时考察了人血的最低检出量。结果血痕的种属与浓度不影响紫外可见反射光谱波峰波谷位置;人血的最低检出量为1.0μL。结论该方法确证血痕具有快速、灵敏、准确、不损坏检材的特点。     

Non-equilibrium pH gradient electrophoresis (NEPHGE) on ultrathin polyacrylamide gels containing separators: improved erythrocyte phosphoglucomutase (PGM) and esterase D (EsD) diagnosis in red cell lysates and bloodstains

Two rapid and reliable electrophoretic techniques for PGM1 and EsD typing on ultrathin polyacrylamide gels are described. They have been based on non-equilibrium pH gradient electrophoresis and on the addition of chemical spacers (EPPS for PGM1 and HEPES for EsD) to the gel mixture.     

Identification of male bloodstains by dot hybridization of human Y chromosome-specific deoxyribonucleic acid (DNA) probe

The sex determination of bloodstains was performed using a human Y chromosome-specific (DNA) fragment of 1.9-kb length as a hybridization probe. The DNA samples were taken from 1- and 4-week-old bloodstains of males and females, respectively. Strong signals with male DNA were observed by Y-probe, while faint signals with female DNA were detected. In addition, clear signals were observed in the extract samples from male bloodstains (16-week-old) on paper. Dot hybridization of the Y-probe would be widely applicable to studies on sex determination of medicolegal materials such as blood, bloodstains, teeth, and cadaverous parts.     

The sexing of bloodstains by testosterone: total protein ratio determination

A simple method for the extraction of testosterone from bloodstains followed by its measurement by radioimmunoassay is described. Complete discrimination of males and females was achieved with measured bloodstains as small as 40 microliters. With stains of unknown volume the total protein content of the stain was determined as an internal reference level. Using the testosterone/protein ratio unequivocal identification was possible for 75% of the stains from males and 50% from females.