abacard p30_semen_miami dade police_adriana kristaly_david smith
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7/21/2019 ABAcard p30_Semen_Miami Dade Police_Adriana Kristaly_David Smith
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Validation of the ne tep B cardTMPS test for the rapid
forensic identification of semen
Adriana Kristaly, BS and David A.S. Smith, MSFS, Forensic Biology Section, Crime
Laboratory Bureau, Miami-Dade Police Department, Miami, Florida.
The visualization of spermatozoa is the most reliable forensic identifier of semen. This
method is obviously ineffective when examining semen from azoospermic or
vasectomized males. Forensic identification of this type of evidence has been
traditionally accomplished by the detection of a unique seminal protein called Prostate
Specific Antigen (PSA) also lmown as p30. The methods used to detect p30 include
immunodiffusion, crossover immunoelectrophoresis and rocket immunoelectrophoresis.
All of these methods are rather complex and time consuming. In this presentation we
examine the
ne tep
ABAcard p30 detection system, a simple and rapid method for the
forensic identification of semen. This poster will present results ITom various studies
including sensitivity, sample size, body fluid mixtures, azoospermic semen and
environmental insults.
The
ne tep
ABAcard PSA test proved to be an effective, sensitive, simple and rapid
method for the forensic identification of semen.
Introduction
The identification of seminal fluid in the absence of spermatozoa is of forensic
importance. This can be accomplished by the detection of unique seminal proteins such
as prostate specific antigen (PSA), also lmown as p30. This is a semen glycoprotein of
prostatic origin with a concentration range of2.0xlO5 to 5.5xlO6nanograms per milliliter
of semen, The
ne tep
ABAcardTMPSA test is designed to qualitatively detect p30 that
could include azoospermic and vasectomized individuals.
In the ABAcardTMPSA test procedure, the p30 antigen reacts with the mobile (dye
particle linked) monoclonal antihuman p30 antibody forming a mobile antigen-antibody
complex, This mobile complex then migrates towards the test ( T ) area where an
immobilized polyclonal antihuman p30 antibody is located. An antibody-antigen-
antibody sandwich is formed when the immobilized antibody captures the above
complex. Ifp30 is present at or above 4 ng/ml in a sample, a pink colored band will form
in the test T area. An internal positive control ( C ) area indicates that the test has
worked properly and proper procedures have been followed. The migrating p30 antibody-
dye complex will not bind to the antibody in the T area but will bind to an immobilized
anti-immunoglobulin antibody in the control c area. The captured pink dye particles
will form a pink band in this area. A single pink colored line in the control c area
indicates a negative result, while two colored lines, one in the test T area and another in
the control c area indicate a positive result (provided no High Dose Hook Effect ).
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