Screening and Serology PPT Flashcards

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1
Q

Screening is the ______ and _______ of evidence for DNA analysis and or preservation

A

Examining and sampling

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2
Q

What are three ways evidence is evaluated before examining?

A

Ensure that the Sub form/ portal receipt is consistent with the evidence packaging and that it is consistent with the DNA Unit Evidence Submission Policy
Determine the Forensic question
Checking communications

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3
Q

“What is the forensic question?”
What are some things to think about in regards to finding the forensic question and how to analyze/examine the evidence?

A

Always “WHO” is on the evidence
But, we need to figure out “HOW do we get the WHO from the evidence” and what does it mean that the WHO was on the evidence

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4
Q

What do you consider when determining the order of examining evidence?

A

Think of the order of DNA concentration. We try to examine evidence in order of low concentration to high concentration

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5
Q

When do you take cuttings as opposed to a swab?

A

When the evidence material is porous such as a shirt and the evidence can penetrate the porous material

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6
Q

What are examples of stuff that you’d take a cutting from?

A

Clothing items for determination of the wearer, staining on fabric, cigarette butts, and adhesive on envelope

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7
Q

When are swabs taken as opposed to cuttings?

A

When evidence is non porous and or if there is expectation that biological material is on the surface of the porous material

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8
Q

What are examples of stuff that you’d take a swab from

A

Clothing for brief contact (on the exterior), plastic, metal, wood, concrete

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9
Q

Where do you take samples on clothing for determining the wearer?

A

collars, waistbands, sleeve cuffs, and interior hat bands

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10
Q

What is the average size of presumptive positive stains that we take through for analysis?

A

1.5cm2 if possible, extracted as trace

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11
Q

What is the size of sample that we take through for determining the wearer?

A

2.0cm2 extracted as Large Volume

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12
Q

What is our screening policy in regards to screening guns based on offenses?

A

P1, we take one swab from the gun and one swab from the magazine and cartridges
P2 we take one swab from the gun

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13
Q

What do we do in regards to multiple cartridge cases?

A

We group them by caliber and area of collection
In the case of cartridge cases, it is okay if there are multiple packages opened at once
We take one swab from each group of cartridges

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14
Q
A
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15
Q

How do we examine bulk consumable items/artifacts?

A

For porous items such as cigarettes, knit gloves, ski masks, and hats, we prepare a cutting to retain some of the item and take 1.5cm2 for analysis
For non porous items, take a swab of the entire item(for bottles, take swab from the mouth area)

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16
Q

What are things to consider when reading SAK paperwork before examining the evidence within the kit?

A

Any contact between the suspect and victim
If there has been any consensual sexual contact within the last 72 hours of collecting the evidence
Any changing of clothes
Time between the offense and the collection of the kit

17
Q

What do we consider as intimate swabs?

A

Swabs from areas of penetration or near areas of penetration

18
Q

What are considered non intimate swabs?

A

areas of potential contact on the body,

19
Q

What is different in regards to the examination of intimate and non intimate swabs?

A

For intimate swabs, they are directly forwarded to a differential protocol
For non intimate swabs, we test each one with Acid Phosphatase. If they are POS, they are forwarded to diff protocol. If neg, all swabs for that sample are taken through a trace protocol in the case that the suspects epithelial cells are present with the victims

20
Q

Describe out process for taking swabs from condoms or sex devices?

A

Take two swabs from each side of the condom.
For sex devices, determine the handle then take one swab from the handle and one swab from the insertion end_-> forward to basic extraction

20
Q

For cases that the bulk clothing or bedding is not ALS POS, where should the item be swabbed if necessary?

A

For underwear, waistband and interior crotch area since a lot of cases involve digital penetration and or no ejaculation

21
Q

How much of a portion is necessary to take through for tissue samples? Hair samples?

A

0.5cm2 for tissue 2-3cm of root end for hairs

22
Q

What is serology?

A

The testing and identification of bodily fluids

23
Q

Name some of the presumptive tests for blood

A

Alder test, Kastle-Meyer/PHE, Ortholidine, LMG, Tetramethylbenzidine test (TMB), Buaiacum, Aloin, Luminol, Bluestar, Fluorescein, ABA card HemaTrace, and Hemastix

24
Q

Name the confirmatory test for blood

A

Microcrystalline test (Takayama and Teichmann)

25
Q

What are some of the positive reasons that we use PHE at LSPCL?

A

Non carcinogen, easy to prepare, it has a higher end of sensitivity compared to other presumptive tests but has fewer false positives. It tests for the presence of hemoglobin in blood

26
Q

What are false positives for PHE?

A

Chemical oxidants (iron or rust), plant peroxidases, tissue, pus or substances of animal origin, warm/hot test samples

27
Q

What are false negatives for PHE?

A

Blood on items that have been washed or bleached, blood on items treated with H2O2

28
Q

What cross reacts with the presence of human blood when considering the HemaTrace test?

A

The weasel family

29
Q

Describe the test process for hematrace?

A

Place sample in buffer for 10-30 mins based on age of sample, place 3-4 drops on card, wait 10 mins to read results

30
Q

What is the high dose hook effect?

A

This occurs when excess antigen binds to the stationary antihuman antibody in the T area of the card. It prevents the antibody-antigen complex from binding. It can be overcome by diluting the sample

31
Q

What are presumptive tests for seminal fluid? Confirmatory tests?

A

Presumptive: ALS, AP, P30 or PSA, ad Florence test; Confirmatory: Microscopy, mRNA

32
Q

What is acid phosphatase?

A

An enzyme secreted by the prostate gland

33
Q

What are false positives for AP?

A

Vegetable/fruit juices, fungi, contraceptive creams, vaginal secretions, yeast infections, male urine, (Spermicides cause ap- results)

34
Q

What is Prostate specific antigen?

A

Glycoprotein found in seminal fluid of humans and some old world monkeys. It can be present in the absence of spermatozoa

35
Q

What is the range of the P30 test? Sensitivity?

A

Range: 200,000 to 5.5 million ng/ml; sensitivity: 4ng/ml

36
Q

When staining spermatozoa, what are the reagents? What are the characteristics of a stained spermatozoa?

A

Kernechtrot (red) and Brilliant green; the tail is green , head is red, and the acrosome cap is clear

37
Q

What reagents start the process of presumptive testingon intimate samples?

A

a 1 hour soak in phosphate buffered saline (PBS) for 30 minutes or longer if the stain is very old

38
Q

What is the purpose of PBS?

A

It is a non toxic solution that allows cellular materials to come off swabs or cuttings