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What else can I help you with?
What other types of controls would be useful to increase reliability of the phenylalanine Deaminase test?
Implementing positive and negative controls, maintaining proper storage conditions for the test reagents, and using standardized testing protocols could help increase the reliability of the phenylalanine Deaminase test. Regularly calibrating equipment and verifying results through a secondary testing method can also enhance the reliability of the test.
Is phenylalanine an acid or a base?
Isoleucine is an amino acid. All amino acids contain an amine functional group, a, carboxylic acid functional group, and a side chain of varying nature. Since amines are generally basic, and carboxylic acids are obviously acidic, there is a self-neutralization of the two groups by themselves. As a side note, the linking of the acid group of one amino acid to the base group of another is called a peptide bond, and is how amino acids are joined to form proteins. Thus, the acidity or bascicity of a pure amino acid in solution is determined by the side chain. Since the side chain of isoleucine is a hydrocarbon (only C-H bonds) which is also neutral, a solution of isoleucine would be neutral as well, with a pH of around 7.
How do you share 3.60 equally?
To share 3.60 equally among a group of people, you would divide 3.60 by the number of people. If there are 3 people, each person would receive 1.20.
If you need to multiply the reaction by 2 to be an intermediate reaction in a hess law problem what would be the final value for the enthalpy of reaction you use for this intermediate reaction?
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Why would running out of Gallium be a problem?
Running out of Gallium would be a problem because it is a key component in certain technologies, such as semiconductors and LEDs. These technologies are widely used in electronics and renewable energy applications, so a shortage of Gallium could disrupt supply chains and hinder technological advancement.
What problem would people have if they did not have phenylalanine hydroxylase?
Phenylalanine hydroxylase deficiency, traditionally known as phenylketonuria or PKU. Untreated it can cause:Intellectual disability, behavioral, emotional and social problems, psychiatric disorders. neurological problems that may include seizures.Fair skin and blue eyes, because phenylalanine cannot transform into melanin — the pigment responsible for hair and skin tone and an abnormally small head (microcephaly).There are different levels of this disorder and a diet very low in proteins can help. This is the first genetic disease that is tested for in infants.
What problem would people have if they did not have phenylalnine?
There is a disease called PKU which is caused by the lack of a working gene that makes an enzyme to break down the amino acid (phenylalanine) which is found in proteins.A person who this rare genetic defect called phenylalanine hydroxylase deficiency, traditionally known as phenylketonuria (PKU) will show signs of intellectual disability (formerly called mental retardation), delayed development, behavioral, emotional and social problems, psychiatric disorders, neurological problems that may include seizures, hyperactivity, poor bone strength, and skin rashes like eczema.Also seen is fair skin and blue eyes, because phenylalanine cannot transform into melanin — the pigment responsible for hair and skin tone and an abnormally small head (microcephaly).Notice that most of the symptoms are due to nervous system damages.
What are the treatments for PKU?
Phenylketonuria is a genetic defect in which a baby is missing phenylalanine hydroxylase, and so prevents the breakdown of certain amino acids found in many proteins.The treatment is a controlled diet that restricts the intake of phenylalanine which would would otherwise build up to damaging levels.Improved answer: according to "Lachel Story, PhD, RN", Pathophysiology, A practical Approach source2012. pg. 26.Treatment for PKU involves a diet low in phenylalanine. Newborns may be breastfed, but the quantity has to be monitored. Special infant formulas are available for supplementation. Dietary restrictions include avoiding proteins and minimizing starches. Oral medications are available to lower phenylalanine (e.g., sapropterin {Kuvan}, and gene thereapy has also demonstrated promise in treating PKU.
What chemical reaction would produce aspartame from aspartic acid and phenylalanine?
Please see this link.
What type of interaction would you expect between phenylalanine and leucine in a tertiary structure?
Phenylalanine and leucine are both nonpolar amino acids, so they would likely interact through hydrophobic interactions in the tertiary structure of a protein. These interactions help stabilize the protein's structure by minimizing contact with water molecules.
What is PKU in biology?
Phenylketonuria (PKU)Is a genetic disease, which is passed on from the mother or father. A associated chromosome is 12. It is a recessive inheritance. Some symptoms may be; irritability, bad odor to skin, vomiting the cause of weight loss, dry skin and itchy rashes, and your skin being senistive to light. The effects it will have on your body may be; weight loss, seizures, mental retardation, head size below normal. Dr. Ivar folling is the discoverer (1934) Tests used to diagnose this disease would be a simple blood or urine test.-Here is some of the information i found. you out, and none of it is false.Sincerely,Gina.
In an individual has no genetic code for phenylalanine?
An individual who cannot produce phenylalanine would not be viable so I believe what you are asking about is Phenylketonuria which is a genetic disorder found is infants who cannot properly digest phenylalanine (they can manufacture it).Hospitals test for this disorder in newborns because it is imperative to place babies that test positive on a strict diet to prevent the mental retardation that is associated with the disorder. Early intervention results in a nearly normal life.
Is hunger a problem in Ireland?
It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.It is not a big problem, but like every modern country in the world, there are some poor people in Ireland who would sometimes be hungry.
If an individual has no genetics code for phenylalanine what kind of danger does it pose to him?
An individual who cannot produce phenylalanine would not be viable so I believe what you are asking about is Phenylketonuria which is a genetic disorder found is infants who cannot properly digest phenylalanine (they can manufacture it). Hospitals test for this disorder in newborns because it is imperative to place babies that test positive on a strict diet to prevent the mental retardation that is associated with the disorder. Early intervention results in a nearly normal life.
What problem would cognitive behavioral therapy be good for?
To treat people
Is the ingredient phenylalanine in stride gum?
Yes, it is in Stride Gum. One place too look would be the back of the container. "Phenylketonurics: Contains Phenylalanine" Also, as a general rule. Most food items do contain it. Beef/Egg whites/fruits (significant amounts in bananas) It is essential to everyone's diet.
Is phenylalanine in Coca Cola Fanta or Sprite bad for your health?
Well its an essential amino acid, so your body needs it, and cannot make it by itself. So you would have to get it from somewhere. Probably Fanta and Coca Cola are bad for your health if you consume enough of it to give you the amount of phenylalanine you need daily though ;)
