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Dit is een voorbeeld van de resultaten en discussie van academische communicatie over CRISPRcas9 en hepatitis B, het kan je helpen om je eigen verslag zo goed mogelijk te maken! Het eerste deel is klassiek geschreven en het tweede deel in de moderne stijl. Zo kan je een goed beeld krijgen van hoe het verslag er ongeveer uit moet zien en hoe je de resultaten moet/kan interpreteren. Dit verslag werd beoordeeld met een 8.00.

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Academische Commu-
nicatie B-B2AS17

Result and discussion section
CRISPR-cas9 efficiently cleaves HBV DNA in the
treatment for hepatitis B virus
In this study the application of the CRISPR-cas9 system on the targeting and cleavage of Hepadnaviridae cc-
cDNA was examined.

Maartje Koppies

1
Universiteit Utrecht, bachelor biologie




Results (classic)

gRNA 3 and 4 most efficient in decreasing antigen concentration
In the first experiment the efficiency of four different guide RNAs, that were able to

target the HBV DNA sequences at different places, was evaluated (1,2,3,4). Firstly, in

the control group an HBV surface antigen (HBsAg) concentration of 8.91 ng/ml +/-

0.2 (n = 20) was measured in the medium of the HBV infected cell lines. Secondly,

the concentration HBsAg that was measured with gRNA 1 (9,24 +/- 0.005 ng/ml; n =

20, p = 0.33) was higher than the control group C. The third gRNA showed a concen-

Citation: Lastname, F.; tration of 3.3 +/- 0.1 ng/ml HBsAg (n=20, p = 0.002)
Lastname, F.; Lastname, F.
Title. Biology 2022, 11, x. And finally, gRNA 4 led to the biggest decrease of antigen con-
https://doi.org/10.3390/xxxxx
centration (2.64 +/- 0.2 ng/ml HbsAg; n = 20, p = 0.002) (Fig-
Academic Editor: Firstname
Lastname
ure 1).
Received: date
Accepted: date
Published: date

Publisher’s Note: MDPI stays
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institutional affiliations.




Copyright: © 2022 by the authors. Sub-
mitted for possible open access publica-
tion under the terms and conditions of
the Creative Commons Attribution (CC
BY) license (https://creativecommon-
s.org/licenses/by/4.0/).



Academic Communication 2022, 11, x. https://doi.org/10.3390/xxxxx

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