Sentences with phrase «protein into»

When you eat a low calorie diet, especially a diet low in carbohydrates, your body breaks down protein into amino acids.
Casein is best as a meal replacement since it's more filling and slowly releases protein into the blood stream.
The final test in this section is for bacterial breakdown of protein into amino acids.
Watch the Full Recipe Video for these 2 Chia Pudding Recipes: Lately, I have been trying to incorporate more plant - based protein into my meals.
By introducing a specific protein into the womb, researchers prevented the defect from taking hold in three children.
Breaking down this protein into amino acids the body can use takes energy, so by co-ingesting protein and carbohydrates you are guaranteeing you'll get the most out of both.
At 6 grams of protein per tablespoon, Gelatin is also an easy way to get some added protein into our diets.
There are so many ways to get this good - for - you protein into your daily diet.
Furthermore, try to include a source of protein into every meal and snack, as protein can also help balance your blood sugar and it has a high thermic effect.
Often when we're trying to «be good» or lose weight, we starve ourselves of carbohydrates (think Paleo and low - carb diets), which encourage our body to convert fat and protein into the glucose our brain needs.
This process efficiently breaks down protein into needed amino acids, allowing for a clean, efficient burn.
Next, they used another virus to insert a gene that put a light - sensitive protein into the amygdala neurons.
Babies and young children can digest mama's milk because they have an active LCT gene that produces lactase in the intestines, a protease that breaks down the lactose protein into more simple sugars as it moves through the digestive system.
We applied an integrated proteomic and genetic strategy by targeting a tandem affinity purification (TAP) tag and Venus fluorescent protein into the endogenous Arc gene in mice.
Inserting it into the nuclear genome helps to protect the gene from oxidative damage, while our tagging system will help guide the functional protein into the mitochondria where it is needed.
The heat of dilution was determined by independent titrations (protein into buffer) and was subtracted from the experimental data.
«It turns out that when you put this protein into the cell, it clears away the damaged tau very nicely,» said Kosik.
«Conversion of the monomeric red fluorescent protein into a photoactivatable probe.»
This molecule cuts the protein into smaller fragments, which float aimlessly around in the cell and wreak havoc on many vital cell structures.
To be able to better measure the properties of the protein, the researchers introduced the genetic information for the BvSUT1 protein into yeast cells or into the ova of an African clawed frog.
By placing aSyn and the huntingtin protein into the library separately and then monitoring each cell's reaction, they were able to deduce which genes are important for the cells to survive the toxic insult from aSyn, and which ones are needed to help the cells survive the huntingtin protein.
Conversion of red fluorescent protein into a bright blue probe.
Conversion of Red Fluorescent Protein into a Bright Blue Probe.
Still, so far all the attempts at converting the full size adiponectin protein into a viable drug have failed.
Howard Hughes Medical Institute researchers have discovered that all the necessary information to sculpt a protein into its proper shape and function is contained in a relatively simple set of...
In the case of the Icelandic mutation though, the alanine is replaced by threonine, which directs BACE1 to cut the protein into shorter strands that are less sticky.
Genetic engineers directly transferred the gene for the toxic protein into crops to give them built - in resistance.
One method is to remove some tumour cells from the patient at the time of surgery, insert a gene for an immune - stimulating protein into them, and return them to the body.
Optogenetics works by inserting the gene of a light - sensitive protein into live neurons, from a single cell to an entire family of them.
Next, using another virus, they inserted a gene encoding a light - sensitive protein into these neurons.
He then places a soluble capsule containing the protein into the hole and seals it with beeswax or plastic film.
The team had also inserted a green glowing protein into the mice that lights up cells during autophagy.
They hypothesized that expressing NeuroD1 protein into the reactive glial cells at the injury site might help to generate new neurons — just as it does in the hippocampus.
Zhang and colleagues engineered the human ubiquitin protein into a new form that paralyses a key MERS enzyme, stopping the virus from replicating.
The combination of both of these changes transform the protein into the one found on the bird flu version of the 1918 virus.
Rather than being toxic itself, it likely is an enzyme that converts a nontoxic protein into something toxic.
To test these predictions, Oka introduced a light - sensitive protein into cells in the SFO, enabling the scientists to selectively activate those cells in the mice.
To find out the role sFlt1 might play, the researchers injected the protein into the tail vein of pregnant rats.
There also a couple of factors that you need to have, as well: You need to have the genetic susceptibility, and you need to have something called a leaky gut, which you can think of as the ability for the intestine to let through this gluten protein into the bloodstream, where it can incite the activity of the immune system and thus create this autoimmune problem.
Computer simulations at the Ohio Supercomputer Center (OSC) helped the researchers visualize what was going on: where the water moved a certain way, the protein folded nanoseconds later, as if the water molecules were nudging the protein into shape.
A prion version of a protein can perpetuate itself in an infectious manner by converting normal forms of that protein into the prion version.
Ironically, these were introduced to Xochimilco in the 1970s and 1980s through programmes run by the Food and Agriculture Organization of the United Nations, with the aim of getting more protein into local diets.
The group inserted an algal gene that codes for a light - responsive protein into mouse embryonic stem cells.
They spliced the gene for this transporter protein into Escherichia coli bacteria and found it enabled the bacteria to pull in presynthesized X and Y bases as well.
Molecular biologist Angela Rmer - Oberdrfer of the Friedrich - Loeffler - Institut in Germany and her colleagues inserted a gene controlling expression of a key flu protein into NDV's genome.
He used this genetically altered version as a Trojan horse to implant the protein into tobacco plants, which could then manufacture their own pesticides.
In their study, the NIAID scientists injected infectious scrapie prion protein into the brains of mice.
Brandis and Hughes changed many different codons and showed that changing even a single codon in the gene for this protein into any one of the alternative «synonymous» codons reduced the «fitness» of Salmonella.
When the researchers injected the protein into the heart muscle of old mice, it became «younger» — thinner and better able to pump blood.
Spiders have been able to turn an insulinlike protein into a powerful poison, for example, thanks to a duplicated hormone gene.
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