Given a sequence, identify palindromic sites that would be recognized by restriction enzymes, identify the axis of symmetry, and be able to draw sequences of fragments that would result from digestions that produce: 3' overhangs, 5' overhangs, blunt ends. Please be thorough with labeling and explaining what the blunt end looks like. Thanks!

Axis of symmetry is nothing just the midpoint of the side. I have marked it on the diagram in blue colour. If your site is 6 bases long, then axis of symmetry will divided into three bases on the right side and three bases on the left side.
Blunt ends are those which do not have any over hangs and after digestion if the restriction enzyme is removed they will not join again. They will remain fragmented.
Sticky ends are those which produce overhang and after digestion if the restriction enzyme is removed they will join again. They will form the intact fragment again.
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Given a sequence, identify palindromic sites that would be recognized by restriction enzymes, identify the axis...
The partial sequences recognized by two restriction enzymes “A” and “B” are indicated below. Complete the sequences such that palindromes are generated for each of the sites. On your palindromes indicate which phosphodiester linkage would have to be cleaved such that 5’ protruding ends of enzyme “A” are compatible with protruding ends of enzyme “B”. Ex. CT/GCAG Enzyme “A”: 5’ATAG― ― ― ― 3’ Enzyme “B”: 5’GCG ― ― ― 3’ Consider your answer to the previous question. A DNA...
Chromosomal and plasmid DNA can be cut into manageable pieces by
restriction enzymes. Using agarose gel electrophoresis, the DNA
fragments can be separated on a gel, based on their lengths. In
order to see the fragments, a stain is typically added to the gel.
The size of each fragment can be determined by comparing each one
to a DNA molecular weight marker of known size.
Below is a map of pBR22 plasmid. The position and base pair
number of the...
please answer all
amils A Doon E Conjagants DNA hips o sloning of freign DA fa ts are called C Clne D Vecto 20 Whatkind of termini is produced by the retriction endonelease Prl, which restriction site has is 5CGATIC (1he dowswd aow represents the site of cleavage in each strand) D Reverse ends E Polylinker termini A.Y ovehan Byaverhang C Blant ends 21.Eeryme dhat cleave DNA at seuence-specifie sites is called D Exonuclease E Integrase A DNA polymerase Ligase...
Identify two restriction
endonucleases that could be used to make sticky ends near the
5’ end of this DNA sequence (upper strand) so that
it could be incorporated into a new plasmid. You have a short list
of them in Table 9-2, and the specific, short sequences of bases
that other enzymes cut at are easily obtained from web resources.
You must cut as near to the 5' end as possible. Indicate the
specific sequences of bases for each endonuclease...
QUESTION 1: You are inserting a gene into an MCS found within the LacZ gene. Using blue/white colony selection, why could you assume that white colonies have modified plasmids? a. A blue colony means the LacZ reading-frame was disrupted b. A blue colony means your gene has mutations c. A white colony means the LacZ reading-frame is intact d. A white colony means the LacZ reading-frame was disrupted QUESTION 2: You are performing a PCR using primers with a sequence perfectly...