This actually shows the scaffold.

Here we take a scaffold, and we basically scaffold can be like a piece of paper here.

And we can then tubularize this scaffold.

You now have your fully seeded scaffold.

We take the cells, we expand them, we place the cells on the scaffold, and we then place the scaffold back into the patient.

We then grow the cells outside the body, take the scaffold, coat the scaffold with the cells the patient's own cells, two different cell types.

Animal protein.

Protein structure is the biomolecular structure of a protein molecule.

We then take a scaffold that we shape like a bladder.

As he's climbing the scaffold, he slips and says, that figures!

A viral protein is a protein encoded by a virus genome.

An antigen is just a protein or part of a protein.

Right here, these green kind of scaffold like molecules, that's chlorophyil A.

Protein DataBank Format

But actually, before placing the scaffold into the patient, we actually exercise it.

And then a few weeks later we can take out the cartilage scaffold.

Miss Plimsoll, how alluring you look, waiting like a hangman on the scaffold.

Just this one protein.

I find the protein.

It's a protein structure.

Found the protein collagen.

So let's say they bond to that special protein, bond to that special protein.

So you have other protein complexes, protein molecular complexes here that also span the membrane.

Marcel Dicke It's all protein.

Animal protein won't allow it.

One can express the active concentration of the protein as the percent of the total protein.

Protein binding is based upon hydrophobic interactions, as well as charged interactions between the membrane and protein.

And we thought it had something to do with this protein called AMP kinase, an energy protein.

Major research efforts in the field include sequence alignment, gene finding, genome assembly, drug design, drug discovery, protein structure alignment, protein structure prediction, prediction of gene expression and protein protein interactions, genome wide association studies, and the modeling of evolution.

In 1981, Lappé relaxed her position on protein combining in a revised edition of Diet for a Small Planet , in which she wrote In 1971 I stressed protein complementarity because I assumed that the only way to get enough protein ... was to create a protein as usable by the body as animal protein.

Now BRD4 is an interesting protein.

RNA provides the information for protein.

Spider silk is almost entirely protein.

It's like a hangover from protein.

Their cones are packed with protein.

Now, BRD4 is an interesting protein.

Preparative methods to purify large amounts of protein, require the extraction of the protein from the electrophoretic gel.

When these small RNA are combined with the protein factors, they make an RNA protein complex called snRNP.

The actual protein might be this big cloud of protein and then your sodiums bond there, there, and there.

Let's say we have a protein here.

This is an MHC class II protein.

And this yellow line represents more protein.

Well folks, we have a protein problem.

And this is a little protein molecule.

What the hell is a sustainable protein?