a slight eletricutional shock I think. not sure. that how we managed 2 make a clone, so I dont see why it wouldn't wor the otehr way.
cheers
-MeRkiLy
A point mutation occurred in the DNA strand. This is a change in a single nucleotide base, such as a substitution, insertion, or deletion.
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
The three types of mutations are substitution (where one base is replaced with another), insertion (where an extra base is added), and deletion (where a base is removed). These mutations can alter the DNA sequence and potentially change the resulting protein.
The mRNA molecule encodes the protein product in the cell for translation. It is a double stranded, base-paired, ribonucleic acid that typically encodes a single gene, or protein, product.
Yes, RNA is typically a single-stranded molecule. It can form secondary structures due to intramolecular base pairing, but it does not typically have the double helix structure seen in DNA.
A Frameshift mutation
a kind of mutation called deletion or insertion
a kind of mutation called deletion or insertion
A one base left out mutation is called a deletion mutation. This type of mutation involves the loss of one or more nucleotides from a DNA sequence, which can lead to a frameshift mutation if not in multiples of three.
The three different types of mutation are substitution, insertion, and deletion. They differ because deletion is missing a base, insertion has a base that was added, and substitution has a base that has been replaced.
A point mutation is when 1 base pair is swapped out for another one... so instead of an A you might find a C... or T... or G. Also an insertion or deletion of a base pair A mutation of a single point :)
A point mutation occurred in the DNA strand. This is a change in a single nucleotide base, such as a substitution, insertion, or deletion.
Because a point mutation is the replacement of a single base with another base. Thus, if the replacement base codes for the same type amino acid, such as a hydrophobic type amino acid replacing a hydrophobic amino acid, no change to the protein coded for will occur. If a deletion mutation occurs then the code for the protein is disrupted and the protein product is probably going to be useless to the body and may even cause a disease.
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
point mutation.
a point mutation
In insertion mutations, an extra base pair is added, and in a deletion, a base pair is taken out (omitted).