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Daily Archives: December 23, 2013
Genetic Engineering – Biology Questions and Answers
Posted: December 23, 2013 at 5:44 am
Learn the Fundamentals of Biotechnology
1. What is biotechnology?
Biotechnology is the application of biological knowledge to obtain new techniques, materials and compounds of pharmaceutical, medical, agrarian, industrial and scientific use, i.e., of practical use.
The pioneer fields of biotechnology were agriculture and the food industry but nowadays many other practical fields use its techniques.
2. What is genetic engineering?
Genetic engineering is the use of genetic knowledge to artificially manipulate genes: It is one of the fields of biotechnology.
3. At the present level of the biotechnology what are the main techniques of genetic engineering?
The main techniques of genetic engineering today are: the recombinant DNA technology (also called genetic engineering itself) in which pieces of genes from an organism are inserted into the genetic material of another organism producing recombinant beings; the nucleus transplantation technology, popularly known as cloning, in which a nucleus of a cell is grafted into a enucleated egg cell of the same species to create a genetic copy of the donor (of the nucleus) individual; the technology of DNA amplification, or PCR (polymerase chain reaction), that allows millions replications of chosen fragments of a DNA molecule.
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Genetic Engineering - Biology Questions and Answers
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Genetic Engineering | The Earth Times | Encyclopaedia
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Genetic engineering is a scientific development that involves the artificial manipulation of an organism's genes by using techniques such as molecular cloning and transformation in order to alter their nature and structure. Many of these transformations are achieved by manipulation of an organism's DNA, which effectively is the code inscribed in every cell to determine how it will function.
As with most scientific developments there are a number of arguments both for and against.
There has been a considerable amount of research into the genetic engineering of crops such as potatoes, tomatoes, soybean and rice, with the aim of obtaining new strains that have better nutritional qualities and better yields.
In a world where there is a continual need to produce more food; genetically engineered crops are being developed to grow on land that is currently not suitable for cultivation. By manipulating the genes in crops the aim is to improve their nutritional value, their rate of growth and their flavour.
Seeds can be engineered so that they are resistant to pests and can survive cultivation in relatively harsh climatic conditions. Biotechnology can also be used to slow down the process of food spoilage so that fruit and vegetables can have a longer shelf life.
Although on the face of it genetic engineering might appear to bring a number of very positive benefits, there is by no means a universal approval of this practice.
Greenpeace International is very firm in its opposition, pointing out that there is no adequate scientific understanding of the impact that genetically modified organisms might have on the world's environment and on human health.
Undesirable genetic mutations can lead to allergies in crops and critics believe that while genetic engineering might enhance taste and appearance of foodstuffs, it could also hamper the nutritional value. At the very least, in order to inform consumers, all foodstuffs or products that have been made from genetically modified food should be clearly labelled as such at point of sale.
Whole new substances such as proteins and other food nutrients can be produced as a result of genetic engineering. The genetic modification of foods can be used to increase their medicinal value, thus making available a range of homegrown medical vaccines.
Greenpeace maintains that commercial interests are the prime movers to introduce genetically modified organisms into the food chain and stresses that once these organisms have been released into the environment they cannot be recalled.
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Genetic Engineering | Buzzle.com
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Genetic Engineering is a very complex field where there is a direct manipulation of an organism's genes. It is also called recombinant DNA technology, which involves creating a DNA by bringing together DNA sequences which otherwise, normally would not be combined. Techniques like transformation and molecular cloning are used in genetic engineering to modify the structure and the characteristics of genes.
Interesting Examples of Genetic Engineering
Genetic engineering is the technique that gives the power to desirably manipulate the genome of an organism. This ability has been explored and experimented in several organisms, some of which have been commercialized whereas the...
Common Misconceptions in Genetics
In the mid-19th century, Gregor Mendel propagated his theories related to heredity. A lot of progress has been made in the field of genetics since then. However, even today, there exist a lot of misconceptions owing to incorrect...
Benefits of Genetic Engineering
Genetic engineering process manipulates the DNA sequence to create a new one. The write-up focuses on the various benefits of genetic engineering.
Genetic Engineering in Humans
With the advancements in the field of genetic engineering, science in the future may give us the power to genetically modify and create 'near perfect' life. Read this write-up to know more about genetic engineering in humans.
Pros and Cons of Genetic Engineering
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Human genetic variation – Wikipedia, the free encyclopedia
Posted: at 5:44 am
Human genetic variation is the genetic differences both within and among populations. There may be multiple variants of any given gene in the human population (genes), leading to polymorphism. Many genes are not polymorphic, meaning that only a single allele is present in the population: the gene is then said to be fixed.[1] On average, biochemically all humans are 99.9% similar to any other humans.[2]
No two humans are genetically identical. Even monozygotic twins, who develop from one zygote, have infrequent genetic differences due to mutations occurring during development and gene copy number variation.[3] Differences between individuals, even closely related individuals, are the key to techniques such as genetic fingerprinting. Alleles occur at different frequencies in different human populations, with populations that are more geographically and ancestrally remote tending to differ more.
Causes of differences between individuals include the exchange of genes during meiosis and various mutational events. There are at least two reasons why genetic variation exists between populations. Natural selection may confer an adaptive advantage to individuals in a specific environment if an allele provides a competitive advantage. Alleles under selection are likely to occur only in those geographic regions where they confer an advantage. The second main cause of genetic variation is due to the high degree of neutrality of most mutations. Most mutations do not appear to have any selective effect one way or the other on the organism. The main cause is genetic drift, this is the effect of random changes in the gene pool. In humans, founder effect and past small population size (increasing the likelihood of genetic drift) may have had an important influence in neutral differences between populations. The theory that humans recently migrated out of Africa supports this.
The study of human genetic variation has both evolutionary significance and medical applications. It can help scientists understand ancient human population migrations as well as how different human groups are biologically related to one another. For medicine, study of human genetic variation may be important because some disease-causing alleles occur more often in people from specific geographic regions. New findings show that each human has on average 60 new mutations compared to their parents.[4][5] Apart from mutations, many genes that may have aided humans in ancient times plague humans today. For example, it is suspected that genes that allow humans to more efficiently process food are those that make people susceptible to obesity and diabetes today.[6]
Genetic variation among humans occurs on many scales, from gross alterations in the human karyotype to single nucleotide changes.[7]
Nucleotide diversity is the average proportion of nucleotides that differ between two individuals. The human nucleotide diversity is estimated to be 0.1%[8] to 0.4% of base pairs.[9] A difference of 1 in 1,000 amounts to approximately 3 million nucleotide differences, because the human genome has about 3 billion nucleotides.
A single nucleotide polymorphism (SNP) is difference in a single nucleotide between members of one species that occurs in at least 1% of the population. It is estimated that there are 10 to 30 million SNPs in humans.
SNPs are the most common type of sequence variation, estimated to comprise 90% of all sequence variations.[10] Other sequence variations are single base exchanges, deletions and insertions.[10] SNPs occur on average about every 100 to 300 bases [10] and so are the major source of heterogeneity.
A functional, or non-synonymous, SNP is one that affects some factor such as gene splicing or messenger RNA, and so causes a phenotypic difference between members of the species. About 3% to 5% of human SNPs are functional (see International HapMap Project). Neutral, or synonymous SNPs are still useful as genetic markers in genome-wide association studies, because of their sheer number and the stable inheritance over generations.[10]
A coding SNP is one that occurs inside a gene. There are 105 Human Reference SNPs that result in premature stop codons in 103 genes. This corresponds to 0.5% of coding SNPs. They occur due to segmental duplication in the genome. These SNPs result in loss of protein, yet all these SNP alleles are common and are not purified in negative selection.[11]
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Human genetic variation - Wikipedia, the free encyclopedia
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Make a strawberry DNA cocktail – Video
Posted: at 5:44 am
Make a strawberry DNA cocktail
It #39;s mixology meets biology. Watch along as TED Fellow Oliver Medvedik walks you through the steps of how to create a yummy adult beverage that isolates stra...
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Make a strawberry DNA cocktail - Video
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DNA profiling – Wikipedia, the free encyclopedia
Posted: at 5:44 am
DNA profiling (also called DNA testing, DNA typing, or genetic fingerprinting) is a technique employed by forensic scientists to assist in the identification of individuals by their respective DNA profiles. DNA profiles are encrypted sets of numbers that reflect a person's DNA makeup, which can also be used as the person's identifier. DNA profiling should not be confused with full genome sequencing.[1] It is used in, for example, parental testing and criminal investigation.
Although 99.9% of human DNA sequences are the same in every person, enough of the DNA is different to distinguish one individual from another, unless they are monozygotic twins.[2] DNA profiling uses repetitive ("repeat") sequences that are highly variable,[2] called variable number tandem repeats (VNTRs), particularly short tandem repeats (STRs). VNTR loci are very similar between closely related humans, but so variable that unrelated individuals are extremely unlikely to have the same VNTRs.
The DNA profiling technique was first reported in 1984[3] by Sir Alec Jeffreys at the University of Leicester in England,[4] and is now the basis of several national DNA databases. Dr. Jeffreys's genetic fingerprinting was made commercially available in 1987, when a chemical company, Imperial Chemical Industries (ICI), started a blood-testing centre in England.[5]
The process begins with a sample of an individual's DNA (typically called a "reference sample"). The most desirable method of collecting a reference sample is the use of a buccal swab, as this reduces the possibility of contamination. When this is not available (e.g. because a court order may be needed and not obtainable) other methods may need to be used to collect a sample of blood, saliva, semen, or other appropriate fluid or tissue from personal items (e.g. toothbrush, razor, etc.) or from stored samples (e.g. banked sperm or biopsy tissue). Samples obtained from blood relatives (biological relative) can provide an indication of an individual's profile, as could human remains which had been previously profiled.
A reference sample is then analyzed to create the individual's DNA profile using one of a number of techniques, discussed below. The DNA profile is then compared against another sample to determine whether there is a genetic match.
The first methods for finding out genetics used for DNA profiling involved restriction enzyme digestion, followed by Southern blot analysis. Although polymorphisms can exist in the restriction enzyme cleavage sites, more commonly the enzymes and DNA probes were used to analyze VNTR loci. However, the Southern blot technique is laborious, and requires large amounts of undegraded sample DNA. Also, Karl Brown's original technique looked at many minisatellite loci at the same time, increasing the observed variability, but making it hard to discern individual alleles (and thereby precluding parental testing). These early techniques have been supplanted by PCR-based assays.
In 1985 (see Mullis and Faloona 1987) a process was reported by which specific portions of the sample DNA can be amplified almost indefinitely (Saiki et al. 1985, 1988). This has revolutionized the whole field of DNA study. The process, the polymerase chain reaction (PCR), mimics the biological process of DNA replication, but confines it to specific DNA sequences of interest.
In this process, the DNA sample is denatured into the separate individual strands. Two DNA primers are used to hybridize to two corresponding nearby sites on opposite DNA strands in such a fashion that the normal enzymatic extension of the active terminal of each primer (that is, the 3 end) leads toward the other primer. In this fashion, two new copies of the sequence of interest are generated.
Repeated denaturation, hybridization, and extension in this fashion produce an exponentially growing number of copies of the DNA of interest. The denaturation is generally performed by heating, and in this case using, replication enzymes that are tolerant of high temperatures (Taq DNA polymerase). Instruments that perform thermal cycling are now readily available from commercial sources. This process can produce a million-fold or greater amplification of the desired region in 2 hours or less.
With the invention of the polymerase chain reaction (PCR) technique, DNA profiling took huge strides forward in both discriminating power and the ability to recover information from very small (or degraded) starting samples. PCR greatly amplifies the amounts of a specific region of DNA, using oligonucleotide primers and a thermostable DNA polymerase. Early assays such as the HLA-DQ alpha reverse dot blot strips grew to be very popular due to their ease of use, and the speed with which a result could be obtained. However they were not as discriminating as RFLP. It was also difficult to determine a DNA profile for mixed samples, such as a vaginal swab from a sexual assault victim.
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DNA Evidence Proves That The First People In China Were Black
Posted: at 5:44 am
Details Published on Monday, 23 December 2013 14:40
The lower part of the face of the Emperor Pu-yi of Manchukuo, direct descendant of the Manchu rulers of China, is most distinctly Negroid/Kulture KriticCHINA is apparently finding out now what Black historians have been reporting for many years, the first inhabitants of China were in fact black.
H. Imbert, a French anthropologist said in his book, Les Negritos de la Chine,The Negroid races peopled at some time all the South of India, Indo-China and China. The South of Indo-China actually has now pure Negritos as the Semangs and mixed as the Malays and the Sakais.
Another author and professor, Chang Hsing-Lang, revealed similar information in writing The Importation of Negro Slaves to China under the Tang Dynasty, Even the sacred Manchu dynasty shows this Negro strain. The lower part of the face of the Emperor Pu-yi of Manchukuo, direct descendant of the Manchu rulers of China, is most distinctly Negroid.
These professors through their research and studies have reason to believe that a Negro Empire actually existed at the dawn of the countrys history citing evidence of substantial populations of Blacks in early China, including finding reports of a major kingdom ruled by Blacks being frequently mentioned in historical Chinese history documents. And,Chinese chroniclers report that a Negro Empire existed in the South of China at the dawn of that countrys history
The notion that blacks were the original inhabitants of China has been thwarted by white scientists and even some blacks as the result of a sweeping message of white superiority and inferiority of black Africans and their descendants spreading worldwide.
Negroid bone structure/Google ImagesIn 2005, DNA testing proved that the first inhabitants of China were black Africans. The study was conducted by a Chinese DNA specialist named Jin Li and a team of Chinese and other scientists. Li admits that he wasnt trying to prove this fact, instead he initially wanted to prove that the Chinese evolved from hmo erectus independently of all humans. After collecting more than 12000 DNA samples from 165 different ethnic groups, Li and his team found that early humans belonged to different species but modern humans had descended from the East African species.
One scientist on the team, Li Hui, said that 100,000 years ago humans began migrating through South and Southeast Asia into China from Africa. Their testing showed that 65 branches of Chinese all carry similar DNA mutations as the people of Southeast Asia.
Another scientist on the team, Jin Li had this to say about their findings, we did not see even one single individual that could be considered as a descendant of the hmo erectus in China, rather, everybody was a descendant of our ancestors from Africa.
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DNA Evidence Proves That The First People In China Were Black
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Human Genome Project Completion: Frequently Asked Questions
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The Human Genome Project Completion: Frequently Asked Questions
On April 14, 2003 the National Human Genome Research Institute (NHGRI), the Department of Energy (DOE) and their partners in the International Human Genome Sequencing Consortium announced the successful completion of the Human Genome Project.
A genome is an organism's complete set of deoxyribonucleic acid (DNA), a chemical compound that contains the genetic instructions needed to develop and direct the activities of every organism. DNA molecules are made of two twisting, paired strands. Each strand is made of four chemical units, called nucleotide bases. The bases are adenine (A), thymine (T), guanine (G) and cytosine (C). Bases on opposite strands pair specifically; an A always pairs with a T, and a C always with a G.
The human genome contains approximately 3 billion of these base pairs, which reside in the 23 pairs of chromosomes within the nucleus of all our cells. Each chromosome contains hundreds to thousands of genes, which carry the instructions for making proteins. Each of the estimated 30,000 genes in the human genome makes an average of three proteins.
Sequencing means determining the exact order of the base pairs in a segment of DNA. Human chromosomes range in size from about 50,000,000 to 300,000,000 base pairs. Because the bases exist as pairs, and the identity of one of the bases in the pair determines the other member of the pair, scientists do not have to report both bases of the pair.
The primary method used by the HGP to produce the finished version of the human genetic code is map-based, or BAC-based, sequencing. BAC is the acronym for "bacterial artificial chromosome." Human DNA is fragmented into pieces that are relatively large but still manageable in size (between 150,000 and 200,000 base pairs). The fragments are cloned in bacteria, which store and replicate the human DNA so that it can be prepared in quantities large enough for sequencing. If carefully chosen to minimize overlap, it takes about 20,000 different BAC clones to contain the 3 billion pairs of bases of the human genome. A collection of BAC clones containing the entire human genome is called a "BAC library."
In the BAC-based method, each BAC clone is "mapped" to determine where the DNA in BAC clones comes from in the human genome. Using this approach ensures that scientists know both the precise location of the DNA letters that are sequenced from each clone and their spatial relation to sequenced human DNA in other BAC clones.
For sequencing, each BAC clone is cut into still smaller fragments that are about 2,000 bases in length. These pieces are called "subclones." A "sequencing reaction" is carried out on these subclones. The products of the sequencing reaction are then loaded into the sequencing machine (sequencer). The sequencer generates about 500 to 800 base pairs of A, T, C and G from each sequencing reaction, so that each base is sequenced about 10 times. A computer then assembles these short sequences into contiguous stretches of sequence representing the human DNA in the BAC clone.
This is intentionally not known to protect the volunteers who provided DNA samples for sequencing. The sequence is derived from the DNA of several volunteers. To ensure that the identities of the volunteers cannot be revealed, a careful process was developed to recruit the volunteers and to collect and maintain the blood samples that were the source of the DNA.
The volunteers responded to local public advertisements near the laboratories where the DNA "libraries" were prepared. Candidates were recruited from a diverse population. The volunteers provided blood samples after being extensively counseled and then giving their informed consent. About 5 to 10 times as many volunteers donated blood as were eventually used, so that not even the volunteers would know whether their sample was used. All labels were removed before the actual samples were chosen.
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Human Genome Project Completion: Frequently Asked Questions
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Secrets Of Longevity In Humans: anti-aging secrets, live …
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What makes up the true factors of longevity? This site focuses on bringing together the best information from a variety of sources such as:
The latest health science and anti-aging research The healthy lifestyle factors found in every longevity society The anti-aging secrets of ancient cultures Instinctual, intuitive and common sense health philosophies
With the overabundance of health information on the internet, it is easy to get caught up in random anti-aging advice that is all theoretical and just plain fraudulent, such as the ridiculous, yet popular notion of taking Tylenol to protect your heart...
If you have enough self-respect to truly pursue human excellence within yourself, then you are going to love what this site has to offer! With humanity's average life expectancy predicted to grow exponentially over the coming years, it is very realistic that super centenarians will be the new 80. Along with living longer, you want to have vitality in these extra years. The information in these pages shows you how to achieve both!
Here are some examples of the types of articles and anti-aging secrets you will be able to find on this site:
~ A list of superfoods and adaptogenic herbs ~ The benefits of mind exercises such as meditation ~ Basic lifestyle habits for a long life ~ Why you don't need to inherit a long life gene ~ Why live, raw foods make up the best type of anti-aging diet ~ How sex and relationships impact your health ~ How you can get a high protein vegetarian diet if you need it ~ Why should people exercise?
"Stacking" a wide variety of healthy lifestyle factors and healthy habits into your daily routine is one of the key antiaging secrets I reveal in these pages. It's time to begin exploring your youth potential!
Embrace Life Without Limits, Zak
P.S. Please feel free to add me as a contact on any of the sites listed below:
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Eczema – Dermatitis Information – Home Health UK Ltd
Posted: at 5:43 am
What is eczema?
The word eczema comes from the Greek and means 'to boil over'. Eczema or dermatitis are two medical terms used to describe numerous skin conditions. Like many allergic conditions the severity of the disease can vary. Although it can sometimes look very unpleasant eczema is not contagious.
What are the symptoms of eczema?
The main symptoms of eczema is skin that is dry, red and inflamed. The area of skin that is affected is often very itchy and in some cases small blisters may form, which can weep and become crusted. Eczema is usually found on the face, hands, the insides of the elbows and the backs of the knees, but it can cover most of the body.
What causes eczema?
The cause of eczema depends on what type you have, read below for more information on the different types. However, in adults, eczema can be triggered off by certain chemicals so care may need to be taken in some jobs. Areas of work with a high risk include: hairdressing, nursing, cleaning, engineering, animal handling or plastering.
Types of eczema
There are many different forms of eczema, which may look and appear very similar but have very different causes.
Two of the most common types of eczema are atopic eczema and contact dermatitis:
Atopic eczema
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Eczema - Dermatitis Information - Home Health UK Ltd
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