Cloning(human cloning) sreenivas.m final pptSreenivas vasu
cloning types in detail .... easy ppt for seminars....................................................................................................................................................................................
Cloning(human cloning) sreenivas.m final pptSreenivas vasu
cloning types in detail .... easy ppt for seminars....................................................................................................................................................................................
Cloning is the process of producing genetically identical individuals of an organism either naturally or artificially.
It is the process of taking genetic information from one living thing and creating identical copies of it. The copied material is called a clone.
Nature has been doing it for millions of years. For example, identical twins have almost identical DNA, and asexual reproduction in some plants and organisms can produce genetically identical offspring.
Cloning in biotechnology refers to the process of creating clones of organisms or copies of cells or DNA fragments (molecular cloning).
Introduction
What is cloning?
Why we want to do cloning?
History
Technique of cell cloning
Dolly – the sheep
Species cloned
Why persue animal cloning research?
Conclusion
Introduction
What is cloning?
Why we want to do cloning?
History
Technique of cell cloning
Dolly – the sheep
Species cloned
Why persue animal cloning research?
Conclusion
A gene knockout is a genetic technique in which one of an organism's genes is made inoperative ("knocked out" of the organism). However, gene knockout can also refer to the gene that is knocked out or the organism that carries the gene knockout. Knockout organisms or simply knockouts are used to study gene function, usually by investigating the effect of gene loss. Researchers draw inferences from the difference between the knockout organism and normal individuals.
this helps to understand the normal techniques related to biotechnology in a simple manner and provides you broad idea about the subject. A brief knowledge about the topic is presented in this presentation.
Cloning is the process of producing genetically identical individuals of an organism either naturally or artificially.
It is the process of taking genetic information from one living thing and creating identical copies of it. The copied material is called a clone.
Nature has been doing it for millions of years. For example, identical twins have almost identical DNA, and asexual reproduction in some plants and organisms can produce genetically identical offspring.
Cloning in biotechnology refers to the process of creating clones of organisms or copies of cells or DNA fragments (molecular cloning).
Introduction
What is cloning?
Why we want to do cloning?
History
Technique of cell cloning
Dolly – the sheep
Species cloned
Why persue animal cloning research?
Conclusion
Introduction
What is cloning?
Why we want to do cloning?
History
Technique of cell cloning
Dolly – the sheep
Species cloned
Why persue animal cloning research?
Conclusion
A gene knockout is a genetic technique in which one of an organism's genes is made inoperative ("knocked out" of the organism). However, gene knockout can also refer to the gene that is knocked out or the organism that carries the gene knockout. Knockout organisms or simply knockouts are used to study gene function, usually by investigating the effect of gene loss. Researchers draw inferences from the difference between the knockout organism and normal individuals.
this helps to understand the normal techniques related to biotechnology in a simple manner and provides you broad idea about the subject. A brief knowledge about the topic is presented in this presentation.
This presentation contains various details from history of cloning to what one should expect in the future from cloning and also different cloning methods
To Clone or not to Clone The Ethical Question Joseph Farnsw.docxturveycharlyn
To Clone or not to Clone: The Ethical Question
Joseph Farnsworth
A couple that had been married for only two years was in a terrible car accident. The
wife walked away with a few cuts and bruises. The husband, however was unconscious
when the paramedics arrived. He went into a coma shortly after arriving at the nearby
hospital. He came out of the coma but was never to be the same again. It turns out that
when he was in the accident he had severe head trauma, and would be a vegetable the rest
of his life. He could not take part in the reproduction of children. The wife is now
distraught because they will never have children together. She heard about the possibility
of cloning and believes that it is the only way that she will ever have children. Is it so?
Introduction
The ethics of human cloning has become a great issue in the past few years. The
advocates for both sides of the issue have many reasons to clone or not to clone. This is
an attempt to explore the pros and cons of human cloning and to provide enough
information of both sides of the arguments in order for the reader to make their own
informed decision on whether human cloning is ethical or not. Cloning will first be
defined. Then a brief explanation of why questions concerning cloning humans have
arisen will be presented. Some things cannot be known for sure unless it is tested, i.e.,
human cloning is allowed. Followed by that, a discussion of the facts and opinions that
support cloning will be presented and then the same against cloning. Please remember
that not all of this has proven true nor is able to be proven yet, but has simply been
argued as a scientific hypothesis. Finally, my own personal opinion will be stated.
Defining Human Cloning
When speaking of human cloning, what is meant? Different groups and organizations
define it differently. To use a specific definition, the American Medical Association
(AMA) defined cloning as “the production of genetically identical organisms via somatic
cell nuclear transfer. „Somatic cell nuclear transfer‟ refers to the process which the
nucleus of a somatic cell of an existing organism is transferred into an oocyte from which
the nucleus has been removed” (Council on Ethical and Judicial Affairs 1). In other
words, cloning is the method of produce a baby that has the same genes as its parent.
You take an egg and remove its nucleus, which contains the DNA/genes. Then you take
the DNA from an adult cell and insert it into the egg, either by fusing the adult cell with
the enucleated egg, or by a sophisticated nuclear transfer. You then stimulate the
reconstructed egg electrically or chemically and try to make it start to divide and become
an embryo. You then use the same process to implant the egg into a surrogate mother
that you would use with artificial insemination. (Eibert)
However, many groups have used a broader definition of cloni ...
This Notes covers Plasmids and Bacteriophages, types, compatibility and infectivity,
Watch this to Learn - https://youtu.be/HhOsWeQjINg
#Vectorsincloning
REPRODUCTIVE ISSUES DUE TO LOW SPERM COUNT.
DIAGNOSIS, TREATMENT, MANAGEMENT AND PREVENTION.
For Scientific Free Lectures, Visit - http://bit.ly/VisitZofirAcademy
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Salas, V. (2024) "John of St. Thomas (Poinsot) on the Science of Sacred Theol...Studia Poinsotiana
I Introduction
II Subalternation and Theology
III Theology and Dogmatic Declarations
IV The Mixed Principles of Theology
V Virtual Revelation: The Unity of Theology
VI Theology as a Natural Science
VII Theology’s Certitude
VIII Conclusion
Notes
Bibliography
All the contents are fully attributable to the author, Doctor Victor Salas. Should you wish to get this text republished, get in touch with the author or the editorial committee of the Studia Poinsotiana. Insofar as possible, we will be happy to broker your contact.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
2. History of Cloning:
1885 -
First-ever demonstration of artificial
embryo twinning.
Sea urchin
Hans Adolf Edward Dreisch
This experiment showed that each
cell in the early embryo has its own
complete set of genetic instructions
and can grow into a full organism.
1902 -
Artificial embryo twinning in a
vertebrate.
Salamander
Hans Spemann
This experiment showed that embryos
from a more-complex animal can also
be “twinned” to form multiple identical
organisms—but only up to a certain
stage in development.
1928 -
The cell nucleus controls embryonic
development.
Essentially the first instance of nuclear
transfer, this experiment showed that the
nucleus from an early embryonic cell
directs the complete growth of a
salamander, effectively substituting for
the nucleus in a fertilized egg.
Salamander
Hans Spemann
3. First successful nuclear transfer
Frog
- Robert Briggs and Thomas King
1952 -
Briggs and King transferred the nucleus from an
early tadpole embryo into an enucleated frog egg
(a frog egg from which the nucleus had been
removed). The resulting cell developed into a
tadpole
Most importantly, this experiment showed that
nuclear transfer was a viable cloning technique.
It also reinforced two earlier observations. First,
the nucleus directs cell growth and, ultimately,
an organism’s development. Second, embryonic
cells early in development are better for cloning
than cells at later stages.
Nuclear transfer from a differentiated cell
1958 -
This experiment showed that, despite previous
failures, nuclei from somatic cells in a fully
developed animal could be used for cloning.
Importantly, it suggested that cells retain all of
their genetic material even as they divide and
differentiate (although some wondered if the
donor DNA came from a stem cell, which can
differentiate into multiple types of cells).
John Gurdon
4. Rabbit
J. Derek Bromhall
This experiment showed that mammalian embryos
could be created by nuclear transfer. To show that
the embryos could continue developing, Bromhall
would have had to place them into a mother
rabbit's womb. He never did this experiment.
First mammalian embryo created by nuclear transfer
1975 -
First mammal created by nuclear transfer
1984 -
This experiment showed that it was possible to
clone a mammal by nuclear transfer—and that the
clone could fully develop. Even though the donor
nuclei came from early embryonic cells, the
experiment was considered a great success.
Sheep
Steen Willadsen
Nuclear transfer from embryonic cell
This experiment added cows to the list of mammals
that could be cloned by nuclear transfer. Still,
mammalian cloning was limited to using embryonic
cells as nuclear donors. Cloning using nuclei from
differentiated adult somatic cells still wasn’t thought
possible
Cow
Neal First, Randal Prather, and Willard
Eyestone
1987-
5. Dolly: First mammal created by somatic cell nuclear
transfer
Of 277 attempts, only one produced an embryo
that was carried to term in a surrogate mother.
This famous lamb, named Dolly, brought cloning
into the limelight. Her arrival started
conversations about the implications of cloning,
bringing controversies over human cloning and
stem cell research into the public eye.
Sheep
Ian Wilmut and Keith Campbell
1996-
1998-1999 - More mammals cloned by somatic cell nuclear transfer
2001 - Endangered animals cloned by somatic cell nuclear transfer
Primate embryonic stem cells created by somatic
cell nuclear transfer
2007 -
This experiment showed that nuclear transfer in
a primate, which researchers had tried for years
without success, was possible. It opened the
door to the possibility of human therapeutic
cloning: creating individual-specific stem cells
that could be used to treat or study diseases.
Rhesus monkey
Shoukhrat Mitalipov and colleagues
6. Human embryonic stem cells created by
somatic cell nuclear transfer
2013 -
In this experiment, researchers took a skin cell
from the patient and fused it with a donated
egg cell. Key to the success of the experiment
were modifications to the culture liquid in
which the procedure was done and to the
series of electrical pulses used to stimulate the
egg to begin dividing.
Shoukhrat Mitalipov and colleagues
No one truly knows the future of human cloning, but many believe
models will be cloned to make designer babies. It is highly probable that a
cloned human being lives among us now. You might read breaking
headlines about cloning but most of those are A few years behind. Some say
they just discovered a new process to human cloning in 2010, but in reality
it was completed in 2005. In 2001, there was such a stir in the human
cloning idea that hundreds of scientist did their work with out anyone
knowing. Thousands of dollars, eggs, adult cells ect. have been donated to
human cloning research. As citizens of the world we can not ignore
scientific research, but instead regulate it. “Either we control gene
technology today, or technology will redesign us by tomorrow.”
Future of Human Cloning
8. Religious issues
Some people believe that cloning is similar to playing God. They believe
that God should be the creator of all living and natural things.
It is believed that a human has the right for the full human development
in a natural environment and that the human embryo should be left alone
after the 14th day of fertilization.
Some religious people believe that if you clone a human being it has no
soul.
People believe human cloning takes away from an Individual being
unique and stresses Psychological and social development.
9. Medical issues
Technically, human gene grows older with age. It’s feared that the
cloned individual would retain the age of the donor’s genes.
Cloning animals through somatic cell nuclear transfer is simply
inefficient. The success rate ranges from 0.1 percent to 3 percent, which
means that for every 1000 tries, only one to 30 clones are made. Some
reasons include
•The enucleated egg and the transferred nucleus may not be compatible
•An egg with a newly transferred nucleus may not begin to divide or
develop properly
•Implantation of the embryo into the surrogate mother might fail
•The pregnancy itself might fail
Problems during later development
•Cloned animals that do survive tend to be much bigger at birth than
their natural counterparts. Clones with LOS(Large Offspring
Syndrome)have abnormally large organs. This can lead to breathing,
blood flow and other problems.
.
10. Abnormal gene expression patterns
• one challenge is to re-program the transferred nucleus to behave as
though it belongs in a very early embryonic cell. This mimics natural
development, which starts when a sperm fertilizes an egg.
• In a naturally-created embryo, the DNA is programmed to express a
certain set of genes. Later on, as the embryonic cells begin to
differentiate, the program changes.
• In cloning, the transferred nucleus doesn't have the same program as a
natural embryo. It is up to the scientist to reprogram the
nucleus Complete reprogramming is needed for normal or near-
normal development. Incomplete programming will cause the embryo
to develop abnormally or fail.
Telomeric differences
• As cells divide, their chromosomes get shorter. The telomere lengths of
cloned animals, found no clear answers. Chromosomes from cloned
cattle or mice had longer telomeres than normal. These cells showed
other signs of youth and seemed to have an extended lifespan
compared with cells from a naturally conceived cow
11. Pros Cons
Defective genes could be eliminated There is a possibility of faster aging.
Faster recovery from traumatic injury There is a reduced sense of
individuality.
Infertility could be eliminated. It may reduce the overall value of
human life.
Cloned body parts can serve as
backup systems for humans
Weaken diversity and ability of
adaptation.
Combat genetic diseases Production of undesirable traits.
Replicate animals for research
purposes & also alterations of plants &
animals
Invites malpractices into society.
Produce people with desirable traits. Humans acting as God
12. World views
Australia
Australia has prohibited human cloning, therapeutic cloning is now legal
in some parts of Australia.
Canada
Canadian law prohibits the following: cloning humans, cloning stem cells,
growing human embryos for research purposes, and buying or selling of
embryos, sperm, eggs or other human reproductive material.
India
India does not have specific law regarding cloning but has guidelines
prohibiting whole human cloning or reproductive cloning. India allows
therapeutic cloning and the use of embryonic stem cells for research
proposes
Argentina
Prohibits:: “experiments concerning cloning of human cells in order to
generate human beings .”
13. REFERENCE
• Wilmut I; Schnieke AE; McWhir J; Kind AJ; et al. (1997). "Viable offspring derived from
fetal and adult mammalian cells". Nature 385(6619): 810–3
• Campbell KH; McWhir J; Ritchie WA; Wilmut I (1996). "Sheep cloned by nuclear transfer
from a cultured cell line". Nature 380(6569): 64–6.
Supported by a Science Education Partnership Award (SEPA) Grant No.
R25RR016291 from the National Center for Research Resources, a component
of the NIH. The contents provided here are solely the responsibility of the
authors and do not necessarily represent the official views of NIH.
• Religious Opposition to Cloning, Journal of Evolution and Technology - Vol. 13 –
October 2003 http://jetpress.org/volume13/bainbridge.htm by William Sims Bainbridge,
Ph.D.
• Bainbridge, William Sims. 2003. "Sacred Algorithms: Exchange Theory of Religious
Claims," in Defining Religion edited by Aurthur L. Greil and David G. Bromley. Oxford:
JAI/Elsevier (Volume 10 of Religion and the Social Order).
• Benin, Mary Holland. 1985. "Determinants of Opposition to Abortion," Sociological
Perspectives, 28: 199-216.
Editor's Notes
Clones are organisms that are exact genetic copies. Every single bit of their DNA is identical. Clones can happen naturally—identical twins are just one of many examples. Or they can be made in the lab. Many people first heard of cloning when Dolly the Sheep showed up on the scene in 1997. Artificial cloning technologies have been around for much longer than Dolly, though.
So lets see how the cloning developed all these days.
1. The sea urchin is a relatively simple organism that is useful for studying development. Dreisch showed that by merely shaking two-celled sea urchin embryos, it was possible to separate the cells. Once separated, each cell grew into a complete sea urchin.
2. Spemann’s first challenge was to figure out how to split the two cells of an embryo much stickier than sea urchin cells. Spemann fashioned a tiny noose from a strand of baby hair and tightened it between two cells of a salamander embryo until they separated. Each cell grew into an adult salamander. Spemann also tried to divide more advanced salamander embryos using this method, but he found that cells from these embryos weren’t as successful at developing into adult salamanders.
3. Again using a strand of baby hair tied into a noose, Spemann temporarily squeezed a fertilized salamander egg to push the nucleus to one side of the cytoplasm. The egg divided into cells—but only on the side with the nucleus. After four cell divisions, which made 16 cells, Spemann loosened the noose, letting the nucleus from one of the cells slide back into the non-dividing side of the egg. He used the noose to separate this “new” cell from the rest of the embryo. The single cell grew into a new salamander embryo, as did the remaining cells that were separated.
1952- The scientists created many normal tadpole clones using nuclei from early embryos. But just like Spemann’s salamander experiments, cloning was less successful with donor nuclei from more advanced embryos: the few tadpole clones that did survive grew abnormally.
1958- Gurdon transplanted the nucleus of a tadpole intestinal cell into an enucleated frog egg. In this way, he created tadpoles that were genetically identical to the one from which the intestinal cell was taken.
1975- Mammalian egg cells are much smaller than those of frogs or salamanders, so they are harder to manipulate. Using a glass pipette as a tiny straw, Bromhall transferred the nucleus from a rabbit embryo cell into an enucleated rabbit egg cell. He considered the procedure a success when a morula, or advanced embryo, developed after a couple of days.
1984- Willadsen used a chemical process to separated one cell from an 8-cell lamb embryo. The he used a small electrical shock to fuse it to an enucleated egg cell. As luck would have it, the new cell started dividing. By this time, in vitro fertilization techniques had been developed, and they had been used successfully to help couples have babies. So after a few days, Willadsen placed the lamb embryos into the womb of surrogate mother sheep. The result was the birth of three live lambs.
1987- Using methods very similar to those used by Willadsen on sheep, First, Prather, and Eyestone produced two cloned calves. Their names were Fusion and Copy.
1996- Dolly was born on 5 July 1996 and had three mothers (one provided the egg, another the DNA and a third carried the cloned embryo to term). She was created using the technique of somatic cell nuclear transfer, where the cell nucleus from an adult cell is transferred into an unfertilized oocyte (developing egg cell) that has had its cell nucleus removed. The hybrid cell is then stimulated to divide by an electric shock, and when it develops into a blastocyst it is implanted in a surrogate mother, Dolly was the first clone produced from a cell taken from an adult mammal. The production of Dolly showed that genes in the nucleus of such a mature differentiated somatic cell are still capable of reverting to an embryonic totipotent state, creating a cell that can then go on to develop into any part of an animal. Dolly's existence was announced to the public on 22 February 1997. It gained much attention in the media. A commercial with Scottish scientists playing with sheep was aired on TV, and a special report in TIME Magazine featured Dolly the sheep. Science featured Dolly as the breakthrough of the year. Even though Dolly was not the first animal to be cloned, she gained this attention in the media because she was the first to be cloned from an adult cell.
After the successes leading up to Dolly and Polly, other scientists wanted to see if similar techniques could be used to clone other mammalian species. Before long, several more animals had been successfully cloned. Among them were transgenic animals, clones made from fetal and adult cells, and a male mouse; all previous clones had been female.
As the list of successfully cloned animals grew, scientists began to explore cloning as a way to create animals belonging to endangered or extinct species. A challenge to cloning endangered and extinct species is finding closely related animals to serve as egg donors and surrogates. The gaur and mouflon were chosen in part because they are close relatives of domestic cattle and sheep, respectively. In 2009, using goats as egg donors and surrogates, another group of researchers cloned the first extinct animal, a Spanish mountain goat called the bucardo. Sadly, the one kid that survived gestation died soon after birth due to a lung defect.
2007- Researchers took a cell from an adult monkey and fused it with an enucleated egg cell. The embryo was allowed to develop for a time, then its cells were grown in a culture dish. These cells, because they can differentiate to form any cell type, are called embryonic stem cells.
Overcoming decades of technical challenges, Mitalipov and colleagues were the first to use somatic cell nuclear transfer to create a human embryo that could be used as a source of embryonic stem cells. The resulting stem cell lines were specific to the patient they came from, a baby with a rare genetic disorder.
Sheep Cloned by Nuclear Transfer from a Cultured Cell Line" (1996), by Keith Campbell, Jim McWhir, William Ritchie, and Ian Wilmut - See more at: https://embryo.asu.edu/pages/sheep-cloned-nuclear-transfer-cultured-cell-line-1996-keith-campbell-jim-mcwhir-william#sthash.BIqOuI3I.dpuf