Genetic engineering
It is called gene replication or gene duplication.
The human gene that encodes insulin is called the INS gene. It is located on chromosome 11 and provides the instructions for producing the insulin hormone, which is crucial for regulating blood sugar levels. Mutations or abnormalities in this gene can lead to diabetes and other metabolic disorders.
The different forms of a gene are called alleles.
In the nucleus of each cell in a firefly's tail, an enzyme called RNA Polymerase finds the DNA encoding the LUC gene within the cell's genome. The LUC gene specifies the squence of amino acids that make up the Luciferase enzyme, which in turn is responsible for the glow we see.
Gene splicing has been done since the 1970s when scientists developed the technique for manipulating DNA. Through gene splicing, specific genes can be inserted, deleted, or modified in an organism's genome. This technology has revolutionized fields such as genetic engineering and biotechnology.
Genetic engineering
I think it's called recombinant technology
Genetic engineering
The expression of a gene is called the phenotype.
It is called gene replication or gene duplication.
Transfection in Farsi means "مهارچه". It refers to the process of introducing nucleic acids, such as DNA or RNA, into a eukaryotic cell for the purpose of manipulating gene expression or studying gene function.
gene flow
A gene that can be masked by another gene is referred to as a recessive gene. This means that the trait associated with the recessive gene is expressed only when two copies of the gene are present.
Different versions of the same gene are called
The gene present on the sex chromosome either in recessive or dormant condition is called a sex linked gene. For example gene for color blindness present on X chrosome. It is carried by a female and mostly affect the male because male have XY type of chromosomal configuration.
The gene present on the sex chromosome either in recessive or dormant condition is called a sex linked gene. For example gene for color blindness present on X chrosome. It is carried by a female and mostly affect the male because male have XY type of chromosomal configuration.
This gene is called a recessive gene. However, there are time when it can show up.