A is wrong.
B is right because that is their job.
C is wrong because that is the B-cells' role.
D is wrong.
Northern blotting is the separation technique that can detect proteins in a complex mixture with the use of antibodies directed against a protein of interest.
Commonly used protein separation techniques include ion exchange chromatography, affinity chromatography, dialysis, ultrafiltration, size exclusion chromatography, and electrophoresis [sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), Isoelectric point electrophoresis, and chromatographic electrophoresis] are included.
Northern blot is a laboratory analysis method for testing RNA. In particular, purified RNA fragments are separated from biological samples (such as blood and tissue) by passing through a gel or matrix like a sieve with an electric current. This allows small fragments to move faster than large fragments.
Northern blotting is named because it resembles Southern blot, the first blotting technique named after biologist Edwin Southern. The main difference is that Northern blots analyze RNA rather than DNA.
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Answer:
B) decreased chromatin condensation
Explanation:
The addition of acetyl groups to the histone tails results in a less packed state of chromatin. The acetylation of multiple Lys residues in the amino-terminal domains of histones H3 and H4 reduces the affinity of the entire nucleosome for DNA. It occurs since acetylation reduces the total positive charge present on histone proteins. Histone proteins are positively charged and pack the negatively charged DNA around them. Therefore, increased acetylation results in decreased condensation of chromatin. The loosely packed DNA is accessible by RNA polymerase and transcription factors for gene expression.
Answer:
Deletion mutations can affect the entire base sequence.
Explanation:
