Because the genetic code is the same in both organisms.
Yes.
1) There are certain aspects of gene expression that are different in eukaryotes and bacteria. The difference can be fixed with an expression vector, a cloning vector that contains a highly active bacterial promoter upstream of a restriction site where the eukaryotic gene can be inserted in the correct reading frame. The bacterial host cell will recognize the promoter and continue to express the foreign gene that is linked to that promoter. 2) Another problem is the presence of non-coding regions, introns, that are in most eukaryotic genes. The intorns make the gene very long and prevents the correct expression of the gene by bacterial cells. [Remember: bacteria does not have the RNA-splicing machinery] This problem is overcome by using a cDNA for of the gene, which includes exons.
a copy of the inserted gene
That gene is a functional unit of DNA. And when it is transformed to another organism it carry out that function there.
A hypostatic gene is one that can by hidden by other genes.
Yes.
the bacterial cell reproduces the bacterial chromosome that the human gene codes for.
The plants will all express the dominant gene.
1) There are certain aspects of gene expression that are different in eukaryotes and bacteria. The difference can be fixed with an expression vector, a cloning vector that contains a highly active bacterial promoter upstream of a restriction site where the eukaryotic gene can be inserted in the correct reading frame. The bacterial host cell will recognize the promoter and continue to express the foreign gene that is linked to that promoter. 2) Another problem is the presence of non-coding regions, introns, that are in most eukaryotic genes. The intorns make the gene very long and prevents the correct expression of the gene by bacterial cells. [Remember: bacteria does not have the RNA-splicing machinery] This problem is overcome by using a cDNA for of the gene, which includes exons.
recessive gene A+
a copy of the inserted gene
No, heat shock is not a method of gene transfer in bacterial cells. Heat shock is a technique used to make cells more permeable to uptake foreign DNA during transformation. Transformation, conjugation, and transduction are the three main methods of gene transfer in bacterial cells.
In Gene clonning copy no of gene increse and translation of each gene produce more no of protein so one can increas production of protein
This phenomenon is based on genetic engineering techniques where the gene for bioluminescence from fireflies is inserted into the tobacco plant's genome. The gene encodes for an enzyme called luciferase, which catalyzes a reaction that produces light. When the gene is expressed in the tobacco plant, it leads to the production of luciferase and the emission of light, making the plant glow.
That gene is a functional unit of DNA. And when it is transformed to another organism it carry out that function there.
Inside bacterial cells, the green fluorescent protein (GFP) is typically encoded by a gene that can be introduced into the bacterial genome or expressed on a plasmid. The gene consists of coding sequences that allow the production of the GFP protein, which fluoresces green when exposed to specific wavelengths of light. The gene is regulated by bacterial promoters and terminators to control its expression level. The GFP protein is then synthesized within the bacterial cell and can be visualized using fluorescence microscopy or other techniques.
An organism can have/carry a gene but without espressing this gene.