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What are the benefits of incorporating RNA/DNA supplements into your daily routine?
Incorporating RNA/DNA supplements into your daily routine can potentially support cellular health, boost energy levels, and promote overall well-being. These supplements may also aid in improving cognitive function, enhancing immune system function, and supporting the body's natural processes of repair and regeneration.
What else can I help you with?
Which macromolecule has a sugar-phosphate backbone?
Nucleic acids DNA and RNADNA has deoxyribose and phosphate forming the backbone and an attached nitrogenous base, These three components form a nucleotide.RNA has ribose sugar, phosphate and nitrogenous bases. The bonds holding the macromolecule together are covalent bonds within the nucleotides and hydrogen bonds holding the double strands of the DNA molecule.
What are two nucleic acids and two differences between them?
There are two kinds of nucleic acids. Deoxyribonucleic acid ,or DNA, is the genetic material that carries information about an organism and is passed from parent to offspring. The information in DNA is also used to direct all of the cell's functions. Most of the DNA in a cell is found in the chromatin in the nucleus. Ribonucleic acid, or RNA, plays an important role in the production of proteins. RNA is found in the cytoplasm as well as in the nucleus.
What are two kind of nucleic acid?
a There are two types of nucleic acids. Purines and Pyrimidines. Purine contains 1) Adenine 2) Guanine. Pyrimidines contains 1)Cytosine 2) Thymine 3)Uracil. Out of this Uracil replaces Thymine in RNA molecule. DNA contains 1) Adenine 2) Guanine 3)Cytosine 4)Thymine.
What is the reason for not getting DNA bands after electrophoresis?
A few reasons you may not see bands on the gel after electrophoresis:DNA concentration too low. More sample has to be loadedDNA sample is contaminated with RNADNA bands are too small and have run out of the gelThe potential (voltage) applied across the gel is not strong enoughThe buffer system in which the gel is suspended is not doing its job correctly. The buffer might have to be made fresh.The electrophoresis apparatus is not in the ocrrect orientation (electrodes not connected to the right poles)Additionally, there could also be other reasons like: improper DNA extraction procedure. If you are running a gel after PCR and still do not see bands, look into whether the DNA is being amplified correctly. See if you are using the correct primers.There are several factors that influence the electrophoresis technique. A close examination of the results obtained will help you make decisions about your future experimental approach.
