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New DNA molecules can come from various sources in gene cloning, such as PCR amplification of a specific gene, synthesis of a gene using recombinant DNA technology, or isolation of a gene from a donor organism. These DNA molecules are then inserted into a vector, such as a plasmid, to create a recombinant DNA molecule for cloning.

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What results from inserting foreign DNA into an organism to produce a new gene combination?

Inserting foreign DNA into an organism can result in the production of a new gene combination known as a transgenic organism. This process can lead to the expression of new traits or proteins in the organism that were not originally present. These transgenic organisms can have applications in agriculture, medicine, and biotechnology.


Which enzyme do scientists use to bond a new gene to plasmid DNA?

Scientists use DNA ligase to bond a new gene to plasmid DNA. DNA ligase catalyzes the formation of phosphodiester bonds between the ends of the new gene and the plasmid, creating a recombinant DNA molecule.


What describes the process of DNA Recombinant?

There are steps you must follow in the making of recombinant DNA such as use crosses to identify donor, clone gene in bacterium, characterize the gene, modify the gene, and reintroduce the gene into donor cells.


Difference between cloning and gene transfer?

Cloning involves creating an identical copy of an organism, while gene transfer involves transferring specific genes from one organism to another. Cloning results in genetically identical organisms, while gene transfer can introduce new traits or characteristics into an organism.


What is the role of the enzymes in cloning?

In cloning, enzymes play a critical role in various steps such as cutting DNA (restriction enzymes), joining DNA fragments (ligases), and replicating DNA (DNA polymerases). These enzymes help manipulate and copy genetic material for creating a genetically identical organism.


A scientist wants to insert new gene into a bacterium what is the first step in this process?

cutting the gene out of the DNA with enzymes


What is the first step in inserting a new gene into a bacterium?

The first step in inserting a new gene into a bacterium is to isolate the gene of interest and prepare it for insertion. This can involve cutting the gene with restriction enzymes and ligating it into a vector, which is a piece of DNA that can deliver the gene into the bacterium.


When a large part of DNA is put into a gene it is a(n)?

When a large part of DNA is inserted into a gene, it is referred to as a "gene insertion" or "gene modification." This process can lead to the addition of new genetic information, potentially altering the function of the gene and affecting the organism's traits. Such modifications can be achieved through techniques like gene editing or recombinant DNA technology.


A scientist wants to instert a new gene into bacterium what is the first step in this process?

cutting the gene out of DNA with enzymes


What bad things happen cause of cloning?

cloning too much of a species can mess up the DNA system and can cause all the new generations to mess up. like the new generations will have new problems they didnt have to face before.


What is DNA manipulation?

DNA manipulation refers to the process of altering an organism's genetic material to achieve desired traits or characteristics. This can involve techniques such as gene editing, cloning, or the introduction of new genes using methods like CRISPR-Cas9. These advancements allow scientists to study gene function, develop new medical treatments, improve agricultural crops, and explore fundamental biological processes. Ultimately, DNA manipulation holds significant potential for various fields, including medicine, agriculture, and biotechnology.


What uses bacteria to copy DNA?

They can reproduce very quickly