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yes - Learnblock
yes - Learnblock

... The aim of the experiment was to show that hydrophobic interactions drive water soluble proteins to fold Intuitively the statement is correct but didn’t they think that before got results? ...
The protein folding problem consists of two parts: 1)Creating a
The protein folding problem consists of two parts: 1)Creating a

... Here is an examples of the helical bundle fold in which we have this double layer of hydrophobic residues in the interior of the protein. ...
gfp - Ana Maria Caputo
gfp - Ana Maria Caputo

... essential nutrients required for cell growth in order to tell if the bacteria were not completely killed because of the shock treatment. Then, some of the sample is added to a place with ampicillin on which only the colonies that contain the plasmid will grow because part of the plasmid codes for th ...


... important residues and helix-packing interactions (11). In general, the biochemical studies correctly identified mechanistically critical residues in the LacY ligand-binding site. However, an additional important observation from the structures of LacY, GlpT, and other membrane proteins is that tran ...
Biotechnology and IP - University of Windsor – EPICentre
Biotechnology and IP - University of Windsor – EPICentre

PYRUVATE DEHYDROGENASE COMPLEX
PYRUVATE DEHYDROGENASE COMPLEX

A novel protein transport system involved in the biogenesis of
A novel protein transport system involved in the biogenesis of

... are an additional determinant that prevents the signal peptide functionally interacting with the Sec pathway [17]. A ¢nal di¡erence between Tat and Sec signal peptide is their length. Sec signal peptides generally comprise no more that 26 amino acids while Tat signal peptides are normally 26^60 amin ...
Efficiency assay of detergent removal columns on - G
Efficiency assay of detergent removal columns on - G

... MS/MS mass spectrometer. TOF mass and product ion spectra were acquired using information dependent data acquisition (IDA) in Analyst QS v1.1 with the following parameters: mass ranges for TOF MS and MS/MS were m/z 300‐2000 and 70‐2000, respectively. Every second, a TOF MS precursor ion spectrum was ...
6. Protiens
6. Protiens

... A. Protein Digestion 1. In the Stomach a. Protein is denatured by hydrochloric acid. b. Pepsinogen (a proenzyme) is converted into its active form pepsin in the presence of hydrochloric acid. c. Pepsin cleaves proteins into smaller polypeptides. 2. In the Small Intestine a. Proteases hydrolyze prot ...
Full Text
Full Text

Translation
Translation

... ___________ molecule serves as the instructions for the order in which amino acids should be joined together to produce a polypeptide. ...
Investigating the role of plant SNFI
Investigating the role of plant SNFI

... 57710. It contains all the invariant residues and conserved domains typical of eukaryotic protein kinases, including the sequence Asp-Leu-Lys-ProGlu-Asn, which is indicative of serinelthreonine specificity [ 111. It is significantly more similar to the SNFl protein kinase than to any other; the GAP ...
Proteomic analyses of the time course responses of mice infected
Proteomic analyses of the time course responses of mice infected

... The membranes were blocked for 1 h at room temperature with 5% skimmed milk in Tris-buffered saline containing 0.1% Tween-20 (TBS-T) to remove nonspecific binding, followed by washing three times for 20 min with TBS-T. The membrane blots were incubated overnight at 4 °C with a 1 : 500 diluted soluti ...
structure_property
structure_property

... The structural elements that allow a sharp change of direction of the polypeptide chain are called reverse turns. Reverse turns are very abundant in globular proteins and generally occur at the surface of the molecule. It has been suggested that turn regions act as nucleation centres during protein ...
2 -1 -2 -1 1 2 K
2 -1 -2 -1 1 2 K

... structure  One or more compact globular regions called domains  The tertiary structure associated with a domain region is also described as a protein fold Multi-domain  Proteins with polypeptide chains fold into several domains  Nearly half the known globular structures are multidomain, more tha ...
DNA and Protein Concentration Measurements Using Fluorescence
DNA and Protein Concentration Measurements Using Fluorescence

... Three Molecular Probes Quant-iT Assay Kits were used to review the Curie’s performance. The Quant-iT PicoGreen dsDNA Assay Kit (P7589) and the DNA Broad Range DNA Assay Kit (Q33130) were used to measure double-stranded DNA (dsDNA) in solution. The Quant-iT Protein Assay Kit (Q33210) was used to meas ...
CHAPTER 5 CARBON CONTENT: LOW LARGE HYDROPHOBIC
CHAPTER 5 CARBON CONTENT: LOW LARGE HYDROPHOBIC

... amino acid pattern which are vital for understanding protein stability and its function as well as these pattern prefers to be folded one with a compact 3D structure. So that the problem of protein-protein & protein –DNA specific interactions, protein-small-molecule interaction and evolutionary unde ...
Reading Pages 136-141: Topics to focus on—
Reading Pages 136-141: Topics to focus on—

... specificity? Tunnel to allow hydrophilic items to pass the membrane that cannot get through the lipid bilayer—very specific (allow glucose but not fructose) 6. Define and explain diffusion. Molecules spread out into available space—random for each molecule but directional for population of molecules ...
Cloning and Sequencing of DNA from a Plasmid Library
Cloning and Sequencing of DNA from a Plasmid Library

... In order to investigate the physiology and central metabolic pathways of Geobacter metallireducens Strain GS-15, a plasmid library of EcoRI-digested chromosomal DNA fragments was constructed in E. coli. A probe for a nirS homolog from Pseudomonas stutzeri and an oligonucleotide probe based on cytoch ...
structural
structural

... The three dimensional structure of the protein is stabilized by all types of bonds between the side chains… ionic between charged AA’s, Hydrogen bonds between polar AA’s, van der Waals forces, and even covalent bonds between sulfurs. ...
Analysis of protein carbonylation
Analysis of protein carbonylation

... interaction with pre-formed reactive carbonyl species). Data in Table 3 are sufficient to illustrate the variety ...
Label-free
Label-free

... -Biomarker research -Tracking specific metabolic pathways -Tracking low abundant proteins in challenging sample (f.ex., in serum) ...
exam 1 1 soln
exam 1 1 soln

... binding Protein X or a problem with deriving energy to transport the molecule? Provide a reason for your choice based on the structure or energy capacity of the nucleotide (i.e. – do not simply refer to the data above). The data show that GTP does not bind Protein X. This is most likely because ATP ...
printed handout sheet
printed handout sheet

... entire system from one state to the other. Insulin reinforces this control by inducing all the key lipogenic enzymes - ATP:citrate lyase, acetyl CoA carboxylase, “malic” enzyme and fatty acid synthase, BUT this takes several hours and the main decision depends on cyclic AMP. ...
h-Barrel membrane protein folding and structure viewed through the
h-Barrel membrane protein folding and structure viewed through the

... for the observation of monomeric and oligomeric states that were resistant to cleavage in the glycine-rich region when bound to the surface of a rabbit erythrocyte, and it was also deficient in pore formation. Membrane binding may occlude the proteolysis sites located in the glycine-rich loop, hinde ...
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Western blot



The western blot (sometimes called the protein immunoblot) is a widely used analytical technique used to detect specific proteins in a sample of tissue homogenate or extract. It uses gel electrophoresis to separate native proteins by 3-D structure or denatured proteins by the length of the polypeptide. The proteins are then transferred to a membrane (typically nitrocellulose or PVDF), where they are stained with antibodies specific to the target protein. The gel electrophoresis step is included in western blot analysis to resolve the issue of the cross-reactivity of antibodies.There are many reagent companies that specialize in providing antibodies (both monoclonal and polyclonal antibodies) against tens of thousands of different proteins. Commercial antibodies can be expensive, although the unbound antibody can be reused between experiments. This method is used in the fields of molecular biology, immunogenetics and other molecular biology disciplines. A number of search engines, such as CiteAb, Antibodypedia, and SeekProducts, are available that can help researchers find suitable antibodies for use in western blotting.Other related techniques include dot blot analysis, immunohistochemistry and immunocytochemistry where antibodies are used to detect proteins in tissues and cells by immunostaining, and enzyme-linked immunosorbent assay (ELISA).The method originated in the laboratory of Harry Towbin at the Friedrich Miescher Institute. The name western blot was given to the technique by W. Neal Burnette and is a play on the name Southern blot, a technique for DNA detection developed earlier by Edwin Southern. Detection of RNA is termed northern blot and was developed by George Stark at Stanford.
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