Genetic engineering
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
This gene is called a recessive gene. However, there are time when it can show up.
A recessive gene.
A piece of DNA that codes for a particular protein is called a gene.
Genetic engineering
Manipulating the arrangement of DNA that makes up a gene is called genetic engineering. This process involves techniques such as gene editing, gene splicing, and gene cloning to alter the sequence of DNA in order to change the characteristics of an organism.
I think it's called recombinant technology
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
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.
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.