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. 2023 Oct 23;13:18105. doi: 10.1038/s41598-023-45366-y

Table 4.

Description of genetic profile of keratinocyte cells after cellular target detection.

Keratincoyte cells
Usability of profile Degradation index Number of missing loci Amelogenin Q/S
Control 2/2

1.2

1

0/22

0/22

X–Y Q/S
Dapi Con A 2/2

0.8

1

0/22

0/22

X–Y Q/S
PNA 2/2

1.2

1.5

0/22

0/22

X–Y Q/S
SNA 2/2

1.2

1.2

0/22

0/22

X–Y Q/S
UEA 2/2

1

1

0/22

0/22

X–Y Q/S
Lam 2/2

0.8

1.3

0/22

0/22

X–Y Q/S
K10 2/2

1.1

0.8

0/22

0/22

X–Y Q/S
Hoechst Con A 2/2

1.2

1

0/22

0/22

X–Y Q/S
PNA 2/2

1.1

1.3

0/22

0/22

X–Y Q/S
SNA 2/2

0.9

1

0/22

0/22

X–Y Q/S
UEA 2/2

1.2

2

0/22

0/22

X–Y Q/S
Lam 2/2

1.1

0.9

0/22

0/22

X–Y Q/S
K10 2/2

1

0.9

0/22

0/22

X–Y Q/S
Anti-H2B Con A 2/2

1

1.1

0/22

0/22

X–Y Q/S
PNA 2/2

0.9

1

0/22

0/22

X–Y Q/S
SNA 2/2

1.1

0.9

0/22

0/22

X–Y Q/S
UEA 2/2

0.8

1.3

0/22

0/22

X–Y Q/S
Lam 2/2

1.2

1

0/22

0/22

X–Y Q/S
K10 2/2

1.5

1

0/22

0/22

X–Y Q/S

The height of the peaks was measured in rfu (relative fluorescence unit): it was proportional to the quantity of PCR products detected. A profile was usable if the number of complete Short Tandem Repeat (STR) markers was greater than 5, according to the requirements of the French database Fichier National Automatisé Empreintes Génétiques. A profile was complete if all STR markers (22 STR) were amplified and present. Degradation index indicated the quality of the DNA (value close to 0: complete degradation; value close to 1: no degradation). Human gender determination was performed by analyzing the amelogenin gene which is common to both X and Y chromosomes. If the two quality sensors (Q and S) were visible on the electrophoregram, it meant that the PCR had been successful and there was no inhibition. 2/2 indicates the number of usable profiles per replicate. Results are representative of at least two independent experiments.