Answer:
The options:
a. Experimentation
b. Analysis
c. Conclusion
d. Hypothesis
The CORRECT ANSWER IS b.
b. Analysis
Explanation:
Good Morning! The scientific process is grouped into stages.
The hypothesis (results from the observation)
The experiment (shows the result of the hypothesis)
The analysis (data is organized and interpreted).
Boom! Our answer is b) Analysis.
Bacteria its important becUse u want to make sure if doesn't contain it.
Nutrients are important because withouth the nutrients in water theres no way for us to have the energy it provides us.
Answer:
1) Altering the DNA of organisms is considered controversial because we do not know what circumstances might occur if the DNA which is being altered turns out to have adverse effect on the organism. There are also concerns that altering the genome and producing organisms with better traits might eradicate the particular wild type organisms on the whole.
2)Yes, there should definitely be a guideline as to who can you the recombinant DNA technology and up to what limits. If guidelines are not set up then it can lead to serious devastating results. We might end up making manipulations which can be very harmful for life. Hence, recombinant DNA technology should be used with much care and under strict guidelines.
3) The techniques in recombinant DNA technology has enable us to make precise changes in the DNA at a higher frequency but certain guidelines shall be set up to control the devastating results which might occur. The concern related to life shall be the first and foremost concern while practicing such techniques.
RNA splicing was first discovered in 1970s in viruses and subsequently in eukaryotes. Not long after, scientists discovered alternative patterns of pre-mRNA splicing that produced different mature mRNAs containing various combinations of exons from a single precursor mRNA. The first example of alternative splicing of a cellular gene in eukaryotes was identified in the IgM gene, a member of the immunoglobulin superfamily. Alternative splicing (AS) therefore is a process by which exons or portions of exons or noncoding regions within a pre-mRNA transcript are differentially joined or skipped, resulting in multiple protein isoforms being encoded by a single gene. This mechanism increases the informational diversity and functional capacity of a gene during post-transcriptional processing and provides an opportunity for gene regulation
