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The S50 Series AC current clamp on CT along with the high content permalloy core makes them well suited for power quality applications.The S50 clamp on ct is a general purpose 1200A AC current clamp designed for use with DMMs & BNC, power loggers and energy meter calibration instruments that have a current input. FEATURES UL, CE CNAS mark; High content permalloy core; Holding wire diameter: φ52mm; Conforms to EN 61010, 600V CAT III; Low phase shift for power measurement; Industrial design & beautiful appearance; Improved ergonomic design & easy operation; Basic parameters : Ratio:1000: 1 , 2000:1, 1000:5 (customized) Accuracy class:0.1%, 0.2%, 0.5% Primary current: 0 - 500A AC and 0-1000A AC Secondary current: 0-1A or 0-5A AC Secondary voltage:0 - 0.5V AC and 0 - 1V AC; Load capacity:≤20Ω, standard 4Ω Over voltage category:CAT III 600V info@gfuve.com 86-15910663251 https: , //www.gfuvegroup.com/ac-current-clamp/1200a-2mhz-b , andwidth-oscilloscope- ac-current-clamp-on-ct.h , tml

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Motor series: low inertia, medium power. Rated output power: 30.0kw. Rated speed: 1500r / min with brake or not: No. Shaft end: Standard (straight shaft). Voltage: 400V type. Protection level: IP65 (p67) hg-sr202bj basic knowledge. Features: low inertia, from low speed to high speed, three modes can be selected, suitable for different application ranges. As a standard production port, hg-sr202bj is installed with 30kW or higher dry flange and feet Application examples: basic knowledge of injection molding machine, semiconductor manufacturing installation, large transmission machinery hg- sr202bj. High resolution encoder 131072p / rev (17 bits). High resolution encoder is included to ensure excellent performance and stability at low speed. All motors are the same size as the previous products and the wiring is compatible. Motor series: low inertia, low power. Rated output power: 0.75KW. Rated speed: 3000r / min. with brake or not: attached. Shaft end: keyway (slotted position). Protection level: IP55, excluding the shaft threading part and the basic knowledge of connector hg-sr202bj. Features: low inertia, suitable for high frequency operation. Application examples: inserter, assembly machinery. Motor series: medium inertia, medium capacity. Use serial pair / incremental encoder. Rated output power: 3.0kw. Rated speed: 1000rpm. With or without band brake: No. Shaft end: straight shaft. The stator structure of AC servo motor is basically similar to that of capacitor split phase single-phase asynchronous motor hg-sr202bj (type selection data). The stator is equipped with two windings whose positions are 90 ° different from each other. One is the excitation winding RF, which is always connected to the AC voltage UF, and the other is the control winding L, which is connected to the control signal voltage UC. Therefore, AC servo motor is also called two servo motors. Motor series: medium inertia, medium power. Rated output power: 3.5kw rated speed: 2000r / min. With brake or not: hg-sr202bj (model selection data) is attached. Shaft end: Standard (straight shaft). Protection level: IP65 (IP67). Features: there are three modes of medium inertia from low speed to high speed, which are suitable for different application ranges. Application examples: transmission machinery, robot, X-Y worktable. High resolution encoder 131072p / rev (17 bit) hg-sr202bj (selection data). High resolution encoder is included to ensure excellent performance and stability at low speed. All motors are the same size as the previous products and the wiring is compatible. Motor series: low inertia, medium power. Rated output power: 6.0kw. Rated speed: 1000r / min. with brake or not: attached. Shaft end: Standard (straight shaft). Protection level: IP65 (IP67) Features: low inertia, from low speed to high speed, three modes can be selected, suitable for different application ranges hg-sr202bj selection manual. As a standard production port, 30kW or higher power is suitable for dry process blue plate (type) installation and foot installation. Basic knowledge of hg-sr202bj. Application examples: injection molding machine, semiconductor manufacturing device, large conveying machinery. High resolution encoder 131072p / rev (17 bits). High resolution encoder is included to ensure excellent performance and stability at low speed. All motors are the same size as the previous products and the wiring is compatible.

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Extracting DNA from blood sounds like a forensic practice we would certainly see on television programs, however what is its energy? While blood is one of the most generally used examples to extract DNA, there are various other sources from which DNA can be removed. What is DNA? To begin with, let's cover what DNA is and its function in the human body. The acronym DNA stands for deoxyribonucleic acid, a complex molecule. This is the basic foundation for an individual's whole hereditary make-up. DNA has the guidelines required to develop as well as preserve life. These directions are written in a code with 4 letters that represent 4 molecules: Adenine (A), Thymine (T), Cytosine (C) and Guanine (G), which are collaborated in a particular way, A joins with T and C with G, forming a dual helix or spiral staircase. The complete series of DNA is called a genome. This is essentially our hereditary code. Every cell in our bodies-- with couple of exemptions-- contains a duplicate of our full genome. You can envision the DNA as one solitary long molecule that is free inside our body's cells yet it is constantly located in the center of the cells and it is also carefully affixed to details proteins. Surprisingly, although all of us have extremely different features from one another, and it is our particular hereditary code what determines our individual attributes, the biggest part of the DNA (99.9%) is the same in all humans. Distinctions in between somatic as well as germline DNA It is essential to set apart in between somatic as well as germline DNA. During embryogenesis all people are created from the union of an egg and a sperm. The genome of the brand-new living being will certainly be made with part of the mommy ´ s as well as the daddy ´ s DNA and all the cells that emerge from the zygote will have the very same hereditary product which is known as germline DNA. As we grow older, it is feasible that tissues may obtain specific genetic variants or anomalies that are not present in the rest of the microorganism, so when we obtain a sample from a specific cells and evaluate its hereditary product, this is known as somatic DNA. This is the reason there may be little differences between somatic and also germline DNA. DNA feature: our genetic code We could specify our hereditary code as our map of life. This indicates that the DNA contains all the required details basic to your growth, reproduction, as well as health and wellness. Moreover, although each cell has the very same info, depending upon its type, the details needed for each and every cell will certainly be activated, from neurons to muscle mass cells. Ultimately, DNA establishes our characteristic traits, from the colour of our eyes to our love of sweets or whether we might be prone to certain injuries or diseases. Taking a look at all these types of information all contained within DNA, it is simple to see its importance for examining it. Any kind of modifications within the DNA series can cause potential illness, vulnerabilities or hereditary characteristics, relying on the type of hereditary variation. Can DNA be removed from blood? We have seen thus far that DNA is present in essentially every cell in our bodies. Consequently, you can draw out DNA from blood-- actually, this is among the most frequently utilized resources for DNA testing. However, leukocytes are the only blood cells that have a center as well as, for that reason, the just one that actually consist of DNA So, extracting DNA from blood indicates analysing the DNA consisted of in leukocytes specifically. Just how is DNA extracted from blood? The first step is to acquire a blood sample which requires a certified person or phlebotomist to carry out the slit. It is a minimally invasive procedure. When the blood example arrives to the laboratory, the service technicians will process the example to obtain the cleansed DNA For this, lots of gadgets as well as equipments are needed, as well as a great deal of reagents. The blood sample is centrifuge which implies that the blood will spin around in an equipment to separate the different components of the blood, so the cells can be easily removed. When the cells have actually been separated, we need to remove the DNA. As you most likely understand, inside the cells we can locate a lots of various organelles and structures that we need to get ride off to detoxify the DNA. For that we need to lyse the cell, which suggests to break all the membrane layers and then include a reagent called protease to eliminate all the proteins. Lastly, nevertheless these procedures we will have our DNA separated. Click to know more about BGI gene test products if you are interested.

Many people have actually heard of genes, yet if you attempt to recognize it thoroughly, it is equally as difficult as discovering Mandarin. The inundation of info can be extremely frustrating when you initially start taking a look at the vast selection of genetic examinations offered online. In truth, everyone has a various factor for wanting to take a genetic examination. Some people want to find out whether they are at threat of dealing with particular diseases, others intend to find out exactly how their genetics might boost their showing off capability, or to discover their genealogical beginnings ... One point is clear when it concerns taking a hereditary examination: the cost mirrors the technology made use of as well as the degree of info it offers you. Every little thing in life has a rate ... so the expense usually gives you a pretty good sign of what you can get out of the test. Not all firms follow the exact same procedure when it involves reading human DNA, the enigma particle that holds the secret to each specific life. If we were to contrast these companies to DNA readers, and also DNA to a book, we might broadly differentiate 3 various kinds of visitor: readers who just check out single words throughout guide, viewers that review 3 or 4 essential web pages, and also those that check out the entire publication. In all three circumstances, the visitors check out actual words, but they acquire entirely various details. In the first case, if the viewers knows precisely which words to look for, they will possibly have the ability to provide you some fascinating info about those words, nevertheless, they will leave out a lot of various other info. We can contrast this to the examinations that just take a look at specific areas of the DNA (tiny variants), naturally linking some spaces in our expertise. These examinations consider extensively researched variations connecting to a certain quality, such as having even more muscular tissue power, having lower vitamin levels, or those revealing ancestral origins. Click to know more about BGI China and BGI gene test products if you are interested.

At-home hereditary testing, or direct-to-consumer (DTC) hereditary testing, can show up to clarify whatever from ancestry and also wellness to run the risk of for severe wellness problems like heart disease, congenital diseases and also cancer. By sending a basic saliva sample, you can have your DNA analyzed as well as get outcomes sent out directly to you. However, it can be tough to analyze every one of the information and recognize what it indicates for your day-to-day life, particularly when the integrity and validity of the information may be vague. Baylor College of Medicine hereditary counselor Tanya Eble supplies ideas on what to take into consideration prior to doing taking an at-home hereditary examination. Evaluate your needs with your physician First, Eble recommends thinking about what you hope to gain from genetic testing. If you have a passion in your ancestry, at-home DNA tests may be an entertainment way to find out more concerning your ancestral tree. But if you want to find out more about your risk for sure health problems or you have concerns about a congenital disease, Eble claims you should speak with your doctor before taking an examination to determine what's right for you. Depending upon your concerns, you might be described a medical geneticist or a genetic counselor. " Genetic testing is just one piece of your threat assessment," claimed Eble, assistant professor of molecular and also human genetics as well as manager of the grown-up genetics clinic at Baylor. "When a client concerns our center for a hereditary analysis, we go through their case history and also a comprehensive family history. We take that information, assess the individual's threat and also determine which examination might be one of the most ideal for them, if any kind of. You miss a great deal of that risk analysis if all you obtain is the record from an at-home test." Take into consideration the scope of the test When taking an at-home hereditary examination, remember that your results might not offer a full photo of your danger for sure health problems. As an example, many examinations try to find anomalies on the BRCA1 and BRCA2 genes, which are connected to enhanced threat of breast as well as ovarian cancer cells. Click to know more about BGI China and BGI gene test products if you are interested.

Huntington's condition (HD) is an acquired problem affecting the mind feature in a progressive manner. This implies that it can be transferred from moms and dads to kids and that its start might begin rather unnoticed, with slow and steady growth affecting the person. A lot of typically, Huntington's symptoms show up in adults aged 35-44. If it develops prior to the age of 20, it is identified as juvenile Huntington's condition. An early-onset implies a little various signs and symptoms and can progress faster than the common HD. Individuals influenced by Huntington's disease normally survive on for regarding 15-18 years after the onset, when it comes to the typical type of the disease, and about 10-15 years for the juvenile HD. Nonetheless, in many cases symptoms are absent until their 50s or 70s. For European populaces, the ordinary occurrence of Huntington's condition is around 9-17:100,000. The disease is less common in other populaces, with values ranging from 0.1 to 2 in 100,000 within native African populations in South Africa, as an example. What causes Huntington's condition? Huntington's condition is triggered by anomalies in the HTT gene. This genetics gives instructions for making huntingtin, a protein that appears to play a vital function in nerve cells in the mind. It was the first disease-associated genetics to be molecularly mapped to a human chromosome in 1983. Especially, the anomaly that creates Huntington's condition is a CAG trinucleotide repeat i.e., a sequence of cytosine, adenine as well as guanine that is repeated numerous times. As a whole, we expect to see 10-35 repeatings of these trinucleotides in the HTT genetics. Nonetheless, in individuals with Huntington's illness, the CAG segment is duplicated 36 to 120 times or even more. Click to know more about BGI gene test products if you are interested.

Genetic tests for genetic cancer cells are created to confirm or eliminate if you have hereditary genetic anomalies that are danger factors for a certain sort of cancer. However what are the benefits of recognizing if you have this predisposition? This short article describes all of it carefully! What is cancer as well as where does it come from? If you have read our articles, "Genetic cancer, can it be avoided?" and "Features of cancer cells as well as hereditary examinations", you will recognize that cancer cells is one of the biggest health and wellness worries affecting culture today, both in regards to the health and wellness effect on sufferers as well as the increase in diagnoses recently: it is estimated that 1 in 3 individuals will certainly establish cancer in their lifetime. What exactly is cancer? Firstly, there are more than 200 sorts of cancer cells, each with extremely various qualities. So why do we utilize the umbrella term "cancer cells"? Because they all have a common measure: exactly how they stem. All cancers take place when cells in a certain tissue begin to multiply frantically. One of the primary troubles with cancer cells is that these cells can migrate from the first cells and also spread to various other parts of the body, where they remain to spread and potentially impair body organ feature, a process known as transition. Cancer cells is a multifactorial illness, which implies that it has both hereditary and also ecological threat variables. The complying with area discusses the influence of genetic factors. The partnership between cancer cells, genes and also inheritance In the write-up "Genes and also chromosomes: just how do they determine our life and our health?", we liken DNA to a publication which contains directions for how our bodies function. Often these directions include mistakes, also known as mutations. And these anomalies, which are changes in the DNA, can bring about various illness, consisting of cancer If one of the a number of genetics that controls cellular division mutates, it can possibly lead to uncontrollable cellular division, causing a tumor. Click to know more about BGI China and BGI gene test products if you are interested.

Did you know that the likelihood of having a boy or a girl is determined by genes? After all, foetal sex relies on whether the sperm cell lugs an X or Y sex chromosome. Do you wish to know why? It's all in this post, where we likewise talk with you about the new techniques for learning the sex of your infant before your 16-week ultrasound scan. What is the hereditary distinction between a women and also a male embryo? We have currently seen this in short articles such as What is DNA?, in each of our cells, humans have 23 sets of chromosomes (overall, 46 chromosomes). The initial 22 pairs of chromosomes are called "autosomal" and coincide in both sexes. However, the chromosomes of set 23 are different in men as well as ladies and also are called sex chromosomes: Pair 23 chromosomes in women: XX. Pair 23 chromosomes in males: XY. The likelihood of having a kid or a girl according to genetics To start with, we should talk a little regarding gametogenesis, which is the process in which sex cells are produced. That is, sperm in the case of men, and eggs in females. These sex cells, i.e. the egg as well as sperm cells, do not include 23 pairs of chromosomes like the remainder of the cells in the body, however have 23 chromosomes each. Therefore, when a sperm cell fertilises an egg, they create a zygote which will certainly have all 46 chromosomes, 23 from the mommy and also 23 from the father. Eggs constantly have an X sex chromosome because, as explained above, females have two X chromosomes. Sperm, nevertheless, can either have an X or a Y chromosome. Therefore, if a sperm with an X chromosome fertilizes an egg, the resulting zygote will certainly be female (XX). On the other hand, if the sperm which fertilizes the egg has a Y chromosome, the zygote will certainly be male (XY). Basically, genetically, the likelihood of having a child or a lady depends on whether the sperm that fertilizes the egg is X or Y. What aspects can affect this process? Now that you recognize exactly how the sex of human beings is established, you may be asking yourself if there are elements that influence whether the sperm that reaches the egg is X or Y. In cases of twin pregnancies, if there is a Y chromosome present, we can figure out that at the very least one of the fetus is male, and if there is no Y chromosome, we can assume that both foetuses are women. Click to know more about BGI China and BGI gene test products if you are interested.

When it involves health as well as condition-- as well as, naturally, several other facets of life-- one thing is particular: genes matter. A single gene mutation can cause some conditions, such as sickle cell anemia and cystic fibrosis. More frequently, several genes are involved in disease advancement, and also they act jointly with nongenetic variables, such as diet regimen or workout, to impact disease danger. A number of companies provide you the chance to consider your genes. However just how might that assist you from a wellness viewpoint? And exactly how do such examinations vary from the hereditary screening a doctor might recommend? Consider the instance of domestic hypercholesterolemia (FH), a problem in which multiple variations of numerous various genes result in considerably high cholesterol. This significantly increases the risk of cardiac arrest, stroke, and other health issue. FH impacts concerning one in 300 adults, which suggests it isn't rare. Among adults that have one of the most usual genetic variants that create it, cardiac arrest or sudden cardiac death may take place in middle age. Children that have a double dosage of a genetics variant linked to this problem might pass away of heart disease before age 20. Earlier treatments intended to reduce the danger of complications, such as cholesterol-lowering medications, are offered if a child or adult is known to have a mutation connected to FH. Hereditary screening gets on the surge Recently, there's been a dramatic increase in hereditary screening. It was virtually uncommon just a few years ago. Currently, you or somebody you recognize has likely had hereditary screening within the in 2015 or more. And while healthcare providers can currently purchase even more genetic tests for their people than in the past, you do not need a doctor's order to request this. 23andMe, BGI China, and a number of other testing firms are ready and also ready to check your genetics for variations associated with specific health conditions, as well as your family origins. In fact, costs on direct-to- consumer hereditary screening is forecasted to reach $2.5 billion within the next couple of years. Click to know more about BGI China and BGI gene test products if you are interested.

During the past century, the scientific area has actually made significant discoveries which played an essential duty in analyzing the human genome: chromosomes were uncovered to be the basis of inheritance; the DNA double helix was seen for the very first time; the organic system by which the cells read the details consisted of in the genes was developed. This last discovery and also the wonderful developments in technology led to the brand-new scientific field of genomics. Ever since, hundreds of genetics and whole genomes have been decrypted. Nowadays, we have learned a significant amount of information regarding genomics, we know more concerning whether a condition is hereditary and just how it may impact us and our youngsters. All this started with the Human Genome Project, which led the way for the application of genomics in analysis and also preventive medicine. What is a genome? Before delving into the background and the innovation behind the Human Genome Project, allowed's establish the basis of what a genome is and the significant role it plays in individualized medication. As covered formerly, DNA is the chemical substance within all our cells that holds the instructions for creating and also creating life. It is mainly made up of 4 nucleotides (to name a few molecules): Adenine (A), Guanine (G), Cytosine (C) and also Thymine (T). These are collaborated in a really particular means: A with T and C with G organized in 2 complementary strands in the form of a double helix appearing like a spiral staircase. The microorganism's full collection of DNA is called the genome. Put simply, the genome is the biological publication of directions forever, including all the info required to establish, function, and duplicate. This code will be transferred from parents to kids. The genome includes all the genetics, the standard units of genes, pieces of DNA that have actually the information required to generate proteins that inevitably accomplish multiple functions in the microorganism. The Human Genome Project In 1990, The Human Genome Task (HGP) was introduced with the goal of figuring out the substantial majority of the human genome. This required the discovery of all human genes and situating them along the genome, along with comprehending the quantity of coding DNA we have, obtaining expertise regarding human advancement, physiology, medicine as well as advancement. Ultimately, the purpose was to advance biomedical research by decoding essential information concerning exactly how the whole genetic product works. To achieve this objective, The International Consortium for Human Genome Sequencing was formed, an open partnership team including twenty centres in six countries to sequence the human DNA. The consortium included numerous researchers at 20 sequencing centres in China, France, Germany, Great Britain, Japan as well as the USA. We might think that this job consisted of sequencing the DNA of a solitary person, nonetheless, this task was carried out with the involvement of numerous volunteers whose identifications have actually been kept secret. Prospects were selected from a diverse populace who provided a number of blood examples. Not all the requested samples were made use of as well as therefore not even the volunteers themselves know whether their DNA was inevitably made use of for this task or otherwise. Click to know more about BGI China and BGI gene test products if you are interested.

Do you know your blood group? This is a question we must all have the ability to address. It includes important details for circumstances such as blood contributions, transfusions or maternities. It is likewise extremely fascinating to understand just how blood groups are inherited, a very common question asked in medical consultations. Do you want to know why? This article clarifies everything: The relationship in between red blood cells and blood group Blood is composed of different cell types put on hold in a fluid called "plasma". Blood is considered a cells as well as consists mainly of red blood cells, platelets, and white blood cells. Blood group are identified by "antigens", which are particles located on the surface of red cell. Each sort of cell does a different feature: Platelets: these cells do not have a center and also are associated with blood clotting when a blood vessel has actually burst. Leukocyte: also called leukocytes, these cells are part of the body's body immune system, battling infection as well as disease. Red blood cells: additionally called erythrocytes, they provide the blood its distinct red colour and also are in charge of moving oxygen as well as carbon dioxide. The antigens that are located on the cell surface develop the various blood groups. Both essential and also popular antigenic systems are the ABO system as well as the RH system The ABO blood group system. The so-called ABO system was uncovered by the Austrian pathologist and also biologist Karl Landsteiner in 1901. Up until that factor, some human to human blood transfusions had been confirmed to be effective and others not, yet the factor was unknown. Click to know more about BGI China and BGI gene test products if you are interested.

CDid you understand that all humans share 99.9% of their hereditary info? This implies our individuality lies in the remaining 0.1%, which varies between individuals and also establishes our physical characteristics (phenotype), in addition to how we react to environmental aspects. Intend to find out even more? In this short article we explore the various types of hereditary modifications which can occur in the genome, as well as just how scientific knowledge and remedies have proceeded considering that the magazine of the whole sequence of the human genome in 2003. Trick Ideas In order to comprehend the feasible genetic modifications that develop our "uniqueness", we should make clear a few key ideas. As we discussed in "Genetics and chromosomes: exactly how do they establish our life and also our health and wellness?" as well as other posts on our blog site, DNA stands for Deoxyribonucleic Acid, a complicated molecule found in the center of the substantial majority of our body's cells. DNA brings the guidelines for the development and procedure of our body's cells: from the colour of our hair to the genetic diseases we might develop. The DNA series is represented in a streamlined way according to the nucleotide base: Adenine (A). Thymine (T). Guanine (G). Cytosine (C). The nucleotides are thus differentiated by their base, and also the DNA sequence is stood for in a streamlined way according to the nucleotide base as A, T, C or G. DNA's structure has two complementary nucleotide strands, which bind in a particular way: A with T and also C with G, and form the nucleotide base sets of DNA. Both chains are wrapped around each other to form a dual helix. Central dogma of molecular biology. DNA includes the directions, but it can not execute all the functions that happen in the body alone. Proteins are in charge of performing these features, as well as the process by which we obtain from DNA to a healthy protein is captured by the main dogma of molecular biology. In the DNA sequence we can find particular locations known as genetics, which include the information for creating proteins. These proteins carry out certain features in the body. There is an entire mechanism within the cells to ensure that this process is carried out properly. First, the DNA is transcribed into carrier RNA (mRNA) in the cell nucleus. In this process the T (thymine) nucleotide is changed by U (Uracil) in the mRNA (single-stranded) leaving the nucleus and, thanks to unique structures called ribosomes, it is equated right into healthy protein which is formed by a series of amino acids. However ... if RNA is formed with a mix of 4 bases and healthy proteins are developed with a mix of 20 various amino acids, how does translation job? The answer hinges on the genetic code described in the 1960s, for which RW Holley, G Khorana and MW Nirenberg were granted the Nobel Reward for medication. In the mRNA sequence the nucleotides are read in 3s, creating a codon that is translated into a details amino acid, as displayed in the table listed below. These "signals" or codons inscribe the amino acids that will create the proteins. Among these, there are 4 unique signals:. AUG: marks the beginning of the translation. UAA, UAG, UGA: these are the quit codons, which suggest that the translation is total. Ultimately, what is the difference in between genome and also exome? The whole set of DNA in a microorganism is called the genome. For humans, the genome has more than 6 billion nucleotides. In fact, if we took the whole DNA series of a single cell as well as stretched it out, it would more than 2 metres long. But of those 6 billion nucleotides, only a small component (approximately 2%) are currently known to contain protein-forming info, that little portion being the exome. Consequently, we define the exome as the coding region of the DNA, while the remainder of the DNA consists of non-coding regions, which do not have info for healthy protein synthesis. So if it does not code for proteins, what is the function of non-coding DNA? For a very long time, it was considered to be "junk DNA", nonetheless, scientific advancements have disclosed that non-coding DNA has several features, the most essential of which is to control the expression of various other genetics. Click to know more about BGI China and BGI gene test products if you are interested.

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