Abstract Bachelorarbeit

[dieulrikemayer]

Hy, am Dienstag muss ich meine Bachelorarbeit abgeben. Könntet ihr bitte meinen Abstract korrektur lesen?

Wood-decay fungi can be identified in different ways. But today there is no way which is fast and cheap as well as reliable and reproducible in identification of contaminated samples. Often samples are contaminated by mould or wood. Whether the method of determination by lengthpolymorphism is a possibility is the ambition of these thesis.
In the ribosomal DNA between the 18S, 5.8.S and 28S-Gene are two non-coding regions, called the Internal Transcribed Spacers. The analysis of 35 referent-fungi showed that every fungi has its own characteristically length ratio between these both spacers. This ratio allows for identify every species. To confirm this ratio, at first the DNS must be isolated form the individual samples and be amplified in the polymerase chain reaction by the help of specific primers. The different length of the ITS-regions are represented electrophoretically.

Vielen Dank für Eure Mühe!

Liebe Grüße Ulrike

[Keswick (Contributor)]

Hy, am Dienstag muss ich meine Bachelorarbeit abgeben. Könntet ihr bitte meinen Abstract korrektur lesen?

Wood-decay fungi can be identified in different ways. But today there is no fast and cheap, and at the same time reliable and reproducible way of identifying contaminated samples. Often samples are contaminated by mould or wood. Whether the method of determination by using lengthpolymorphism is a possibility (a possibility to do what? please add) is the ambition of these thesis.
There are two non-coding regions in the ribosomal DNA between the 18S, 5.8.S and 28S-Gene called the Internal Transcribed Spacers. The analysis of 35 referent-fungi showed that every fungi has its own characteristically length ratio between these both spacers. This ratio allows the identification of every species. To confirm this ratio, at first the DNS must first be isolated from the individual samples and with the help of specific primers be amplified in the polymerase chain reaction. The different lengths of the ITS-regions are represented electrophoretically.

Vielen Dank für Eure Mühe!

Liebe Grüße Ulrike

[Duckduck (Contributor)]

Hy, am Dienstag muss ich meine Bachelorarbeit abgeben. Könntet ihr bitte meinen Abstract korrektur lesen?

Da fiel mir noch das eine oder andere auf, Ihr Lieben!

Though wood-decay fungi can be identified in different ways, there is no fast, cheap, and at the same time reliable and reproducible way of identifying them in samples contaminated by mould or wood to date. The aim of this thesis is to find out, whether the determination of wood-decay fungi by using lengthpolymorphism is a possible solution to this problem.
There are two non-coding regions in the ribosomal DNA between the 18S, 5.8.S and 28S-Gene called the Internal Transcribed Spacers. The analysis of 35 referent-fungi showed that every fungus has its own characteristically length ratio between these two spacers. This ratio allows the identification of every species. To confirm this ratio, at first the DNA must first be isolated from the individual samples and then be amplified in the polymerase chain reactionby using specific primers. The different lengths of the ITS-regions are represented electrophoretically.

Vielen Dank für Eure Mühe!

Liebe Grüße Ulrike

Das sind so meine Gedanken dazu...

Viel Glück für Dienstag!
Duckduck

[dieulrikemayer]

Vielen lieben Dank für eure Korrekturen.

Liebe Grüßen Uli