To transform the mice, you can:
1. inject the gene into the cells with microscopically small needles
2. use electroporation (an electical pulse that creates temporary pores in the plasma membranes of the cells that DNA can go through)
3. use a powerful virus
We as humans have successfully cloned a sheep I am sure the name 'Dolly' comes to mind. But as for cloning another human being; ethics has gotten in the way of such an achievement, but it IS possible.but scientists observed that a cloned being is prone to infections and diseases..
there is no specific animal but they've cloned about 100 animals like sheep, pigs, cats, mice, cows,rabbits, and goats
Changes in the mice are most likely due to genetic modification through gene editing techniques like CRISPR-Cas9. This process involves altering the genetic material in the mice to produce specific traits or characteristics.
White fur color is recessive and brown is dominant. The white mouse has a genotype of bb and the brown mouse has a genotype of BB. All offspring would be heterozygous with a genotype of BB and brown fur.
Mice are rodents.
There is belief that you have to do it with the successful combination of dna with mice. If it isn't that, then you don't get the results you want to have with that object.
Uterus
cattles ,pigs ,mice and dolly a sheep the first maMMAL TO BE CLONED
Yes, scientists have successfully cloned animals such as sheep, cows, pigs, and mice. The most famous cloned animal is Dolly the sheep, who was cloned in 1996. Cloning technology has advanced since then and has been used for various research purposes.
A gene from a firefly
Knock out mice are produced by impairing or deleting a particular gene expression. Thus the gene function (which was deleted) can be tracked by studying this knock out and the control mice. Lets say a gene is suspected to trigger immune response against a pathogen, one can study this by infecting the wild type(normal) and knock out(specific gene deleted) mice and study the role of the gene.
Knock out mice are produced by impairing or deleting a particular gene expression. Thus the gene function (which was deleted) can be tracked by studying this knock out and the control mice. Lets say a gene is suspected to trigger immune response against a pathogen, one can study this by infecting the wild type(normal) and knock out(specific gene deleted) mice and study the role of the gene.
In 1977, Karl IIlmensee created a mice with only one parent.On Oct 3, 1997, the Honolulu Technique created Cumulina the cloned mouse. She was cloned from cumulus cells (cells which surround developing egg cells) using traditional nuclear transfer. The nucleus was taken from the cumulus cell and implanted in an egg cell from another mouse.
of course those were they're first specimins. most of which died from phemonia or lived for 800 days
the gene integrated into the mice chromosomes and expressed itself; thus making the mice grow up to be larger than normal.
Yes, but that does not mean that any viable creature might develop. There are very few limits to what genes can be inserted into what - quite a few creatures have gained fluorescing genes from jellyfish, including mice, and antifreeze genes from an arctic fish have been inserted into a soft fruit (raspberries I think).
it has been suggested that DNase1, part of the "junk" DNA in the nucleus, is responsible. I recall an experiment with mice where this gene was turned off and mice started presenting with signs of SLE.