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Miscellaneous Bioseparation
Miscellaneous Bioseparation

... Moreover, most proteins bind a constant amount of ion, so that the net charge per protein is well regulated Under these conditions, different proteins in a mixture may be separated according to size only The molar mass of each constituent protein is estimated by comparing its mobility in its rod-lik ...
JSB-302
JSB-302

... The JSB-302 is designed for nucleic acid screening electrophoresis. The maximum suggested applied voltage for the electrophoresis of DNA in agarose gels using the JSB-302 is 150 volts. In a 1% TBE gel, this translates into a run time of approximately 1 hour. Lower voltages may be used, of course, an ...
CH 3 RG 2014 Carbon and the Molecular Diversity of Life
CH 3 RG 2014 Carbon and the Molecular Diversity of Life

... 8. Enzymes are globular proteins that exhibit at least tertiary structure. As you study Figure 3. In your text, use this figure to identify and explain each interaction that folds this protein. ...
Department of Microbiology, Lab 016 instructions Standard gel
Department of Microbiology, Lab 016 instructions Standard gel

... Standard agarose 1-1,5 %. Dissolve 1-1,5 gram in 100 ml 1xTAE buffer (diluted with Aqua dest from a 100 x stock solution). Heat in micro oven. Pour the gel and select appropriate combs to produce wells of desired size. TAE-Puffer (100x): 4 M Tris, 1 M Natriumacetate, 0,1 M EDTA. Mix with Aqua dsest. ...
w12-proteins
w12-proteins

... o Useful for small sets of specific proteins (e.g. cytokines)  2D gels separate a protein mixture based on two properties, typically size and pH/charge o Compare 2D coordinates to reference positions for identification  Tandem mass-spectrometry (MS-MS) = shotgun sequencing for proteins o Protein m ...
The basis of specific ligand recognition by proteins
The basis of specific ligand recognition by proteins

... Interfaces of molecular complexes with proteins exhibit significant and relevant mobility, also referred to as fluctuating networks of interactions; these often involve water molecules with very short residence times. The general problem of mobility will be addressed by specifically looking at inter ...
Prediction practice - unlinked
Prediction practice - unlinked

... Gel electrophoresis • Used to separate fragments of DNA or proteins according to size (uses an electric field to separate charge molecules) DNA is all negatively charged so everything moves in the same direction. Small fragments move faster, so in a given time they will move a greater distance. ...
Precipitation of Proteins at isoelectric Point
Precipitation of Proteins at isoelectric Point

... Precipitation of Proteins at isoelectric Point Protein solubility • There are many factors that contribute to protein solubility. • The most important determinant its electrostatic charge. • The solubility of proteins in aqueous buffers depends on the distribution of hydrophilic and hydrophobic ami ...
Mass Spectrometry
Mass Spectrometry

... A potential application of MS is for the early detection of certain cancers. MALDITOF-MS offers the opportunity to rapidly detect and monitor oncoprotein expression against a background of normal protein activity An promising application of MS is the analysis of tissue samples for molecular distribu ...
BIOMOLECULES UNIT 3 Chemistry Review: Atoms
BIOMOLECULES UNIT 3 Chemistry Review: Atoms

... Ionic- electron stealing Covalent- electron sharing Van der Waal’s forces- attraction between positive and negatively charged ions that cumulatively are strong, (Gecko feet), but not as strong as the other types. Hydrogen bonds- attraction between water molecules, and other molecules Elements- pure ...
Proteins*
Proteins*

... What do you think is happening to the proteins within these eggs???? ...
Name Period
Name Period

... 1. An ionic bond forms when electrons are 2. A covalently bonded compound is formed by the 3. What is a polar molecule? 4. How does a hydrogen bond form? 5. What is adhesion? 6. What is cohesion? 7. What is high specific heat? 8. What is heat of vaporization? 9. What is unique about the freezing of ...
Cell Building Blocks
Cell Building Blocks

... The term is more-specifically used to refer to fatty-acids and their derivatives (including tn-, di-, and mono-glyccrides and phospholipids) as well as other fatsoluble sterol-containing metabolites such as cholesterol. Lipids serve many functions in living organisms including energy storage, serve ...
Review For Final I - NAU jan.ucc.nau.edu web server
Review For Final I - NAU jan.ucc.nau.edu web server

... • divide the difference by 40 for the percent score you need ...
Activities 3
Activities 3

... Lysine Tyrosine Glutamate Isoleucine ...
SOLUGEL Protein Gummies Leaflet
SOLUGEL Protein Gummies Leaflet

... Triple your gummies’ protein content with SOLUGEL®! The traditional gummy bear contains around 6g of protein per 100g, entirely from its gelatin content. With SOLUGEL®, it is now possible to create a gummy rich in collagen protein that looks and tastes like any other gelatin gummy, but contains more ...
2.4 review
2.4 review

... 3) Discuss why the same 20 amino organisms are used by most organisms to make proteins. 4) Distinguish between a polypeptide and a protein. 5) What is an “R” group? How many different ones are there? 6) Give an example of the largest and smallest proteins in the human body and their relative size. 7 ...
SDS-PAGE and Western blotting
SDS-PAGE and Western blotting

... Fig.1Before SDS:  Protein (pink line) incubated with the denaturing detergent SDS showing negative and  positive charges due to the charged R‐groups in the protein.  The large H's represent hydrophobic domains where nonpolar R‐groups have collected in an attempt to get  away from the polar water th ...
Biological Molecules
Biological Molecules

... •All of these organic molecules always contain the elements Carbon (C), Hydrogen (H) and Oxygen (O). Proteins contain Nitrogen as well, and sometimes sulfur. Nucleic acids have C, H, O, N and phosphorus (P). ...
Tris-Borate-EDTA buffer
Tris-Borate-EDTA buffer

... RNase/DNase activity Format Composition Volume pH (25°C) Shelf life ...
Standard B-2
Standard B-2

... of a chemical reaction; is not consumed or altered during a chemical reaction, so, it can be used over and over again. o Enzymes: proteins that serve as catalysts in living organisms. o Enzymes are very specific. Each particular enzyme can catalyze only one chemical reaction by working on one partic ...
HS SDS-PAGE (msword 21,1 kB)
HS SDS-PAGE (msword 21,1 kB)

... front of the fume hood. In case of a long power or ventilation failure the lab must be evacuated. 4. Run the gel (electrophoresis) Ensure all equipment is in good working order, and that lid is always on electrophoresis tank when in operation. It is important to note that the voltage and currents us ...
Document
Document

... c.) in the promoter? Ask yourself—What acts at the promoter?! RNA Polymerase…Okay, there are some critical regions in the promoter (namely –10 and –35) that serve as binding sites for RNA Polymerase. If those were mutated, could that possibly result inproduction of a non-functional protein? YES! Mut ...
TABLE 3–1 Some Common Types of Enzymes
TABLE 3–1 Some Common Types of Enzymes

... catalyze the rearrangement of bonds within a single molecule. catalyze polymerization reactions such as the synthesis of DNA and RNA. catalyze the addition of phosphate groups to molecules. Protein kinases are an important group of kinases that attach phosphate groups to proteins. catalyze the hydro ...
3.2 Proteins - Biology with Radjewski
3.2 Proteins - Biology with Radjewski

... • Disulfide bridges hold a folded polypeptide together • Hydrogen bonds stabilize folds • Hydrophobic side chains can aggregate • van der Waals interactions between hydrophobic side chains • Ionic interactions ...
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QPNC-PAGE

QPNC-PAGE, or quantitative preparative native continuous polyacrylamide gel electrophoresis, is a high-resolution technique applied in biochemistry and bioinorganic chemistry to separate proteins by isoelectric point. This standardized variant of native gel electrophoresis is used by biologists to isolate active or native metalloproteins in biological samples and to resolve properly and improperly folded metal cofactor-containing proteins or protein isoforms in complex protein mixtures.
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