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Dąbrowska, Grażyna ; Veit, Justyna ; Goc, Anna ; Tretyn, Andrzej
Committee on Biotechnology PAS ; Institute of Bioorganic Chemistry PAS
The Pharbitis nil cDNA about 165 bp was identified by differential display method. Screening of the P. nil cDNA library allowed to find homologous clone PnCAT-L 985 bp in length. Sequence analysis of P. nil cDNA indicated that the identified clone has 81% homology to Zea mays and Campylobacter jejuni catalase genes. The expression of the catalase-like gene is elevated in cotyledons of A nil plants cultivated under continuous light conditions.
Biotechnologia, vol.65, 2 (2004)-.
application/pdf ; application/pdf
0860-7796 ; oai:rcin.org.pl:122351
Library of Institute of Bioorganic Chemistry PAS
Creative Commons Attribution BY-SA 4.0 license
Institute of Bioorganic Chemistry of the Polish Academy of Science
Institute of Bioorganic Chemistry of the Polish Academy of Science
Oct 2, 2020
Apr 29, 2020
45
https://rcin.org.pl./publication/152714
Edition name | Date |
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Podobny do katalazy gen Pharbitis nil ulega podwyższonej ekspresji u roślin uprawianych na świetle ciągłym | Oct 2, 2020 |
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