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Parallel analysis of translated ORF (PLATO)
Parallel analysis of translated ORF (PLATO)

... Procedure :-Baits bound on a support -Molecule of interest is tagged with a fluorescent dye -Detection by fluorescence >Pattern of +/-spots >Signal intensity is proportional ...
Macromolecules Worksheet #2
Macromolecules Worksheet #2

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No Slide Title

... Protein folding is a “grand challenge” problem in biology the deciphering of the second half of the genetic code, of pressing practical significance Problem 1: given a protein’s amino acid sequence, predict its 3D structure, which is related to its function Problem 2: “… use the protein’s known 3D s ...
Chemiluminescent and Fluorescent Westerns
Chemiluminescent and Fluorescent Westerns

... across a variety of laboratories, and many facilities provide the necessary darkroom and developer for documentation with x-ray film. The technique is popular because it is relatively easy to perform and can be extremely sensitive; substrates can be purchased that detect proteins in the femtogram ra ...
His-tag pull-down assay Possible interaction between PprI protein
His-tag pull-down assay Possible interaction between PprI protein

... Possible interaction between PprI protein and N-terminal part of DdrO(N-DdrO, a.a. 1-108)were tested using His-tag pull-down assay. 20 µg of purified N-DdrO protein with N-terminal His-tag was incubated with Ni-NTA agarose beads in 1 ml of pull-down buffer (167mM NaCl, 20 mM Tris-HCl pH 8.0, 5% glyc ...
Stimulation of G-Protein-linked Receptors Activates G
Stimulation of G-Protein-linked Receptors Activates G

... Some G Proteins Regulate Ion Channels The target proteins for G-protein subunits are either ion channels or membrane bound enzymes. Different targets are affected by different types of G proteins, and these various G-proteins are themselves activated by different classes of cell surface receptor. I ...
MCB100A/CHEM130A In-Section Quiz #2 (Aathavan Karunakaran)
MCB100A/CHEM130A In-Section Quiz #2 (Aathavan Karunakaran)

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The Body`s Essential Building Blocks, Article by Gloria Gilbère, N.D.
The Body`s Essential Building Blocks, Article by Gloria Gilbère, N.D.

... proper pH balance in the gastrointestinal tract and body tissues. Scientific research confirms that proAUTHORS NOTE biotics are a vital necessity in the supThose that follow my work and writings know port of overall human health, that I credit goat-milk products for a major role in my specifically d ...
Solid Tumour Section Kidney: t(X;17)(p11.2;q23) in renal cell carcinoma
Solid Tumour Section Kidney: t(X;17)(p11.2;q23) in renal cell carcinoma

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Group : Nanochemical Biology Project : Tyrosine cross

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Muscle Juice 2544 - Ultimate Nutrition
Muscle Juice 2544 - Ultimate Nutrition

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Seminar L11- Laboratorija za molekularno biologijo in
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... This presentation gives a brief overview on Microscale Thermophoresis (MST), a new technology to study biomolecule interactions. The term Microscale Thermophoresis refers to the directed movement of molecules in optically generated microscopic temperature gradients. This thermophoretic movement is d ...
A1991FN73000001
A1991FN73000001

... I was genuinely delighted by these result, and believed that a method had been hamd for protein sequencing at the picomole level. I was eager to Ibid an application toprove it. In 1978, I brought the DA811C method to the lab of L Wittmann-Llebold at the Max Planch Institute in Berths. There, I relbi ...
lecture08_12
lecture08_12

... Where it is expressed ? Motif (or fingerprint): • a short, conserved region of a protein • typically 10 to 20 contiguous amino acid residues ...
Tertiary Structure to X-Ray Crystallography
Tertiary Structure to X-Ray Crystallography

... very middle of the structure of 3EWC is a bound molecule, visible in the center of the structure. This bound molecule blocks of the function of adenosine deaminase and inhibits its function. Since tertiary structure describes the three-dimensional shape of a protein, another level of protein structu ...
week 5 no answers
week 5 no answers

... Denaturants => cause large, structural change and loss of function i. Usually cause abrupt loss of function -> protein unfolding is cooperative. ii. Important- > do not break covalent Denaturants will distrupt hydrophobic interactions. Eg. _____________________? ___________________________? Experime ...
g-protein-coupled-receptor-presentation
g-protein-coupled-receptor-presentation

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An Introduction to Protein Structure Databases
An Introduction to Protein Structure Databases

... The superposition of 2 (or more) 3D structures, so that as many atoms as possible match. Alignment usually only by c-alpha atoms. 3D alignments are not sequence alignments, but they can converted into sequence alignments. Structural alignment also important for evolutionary comparisons and functiona ...
Spectrophotometric methods for determination of proteins
Spectrophotometric methods for determination of proteins

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STUDIES ON MAMMALIAN MATURATION ANTIGEN(SMA2)
STUDIES ON MAMMALIAN MATURATION ANTIGEN(SMA2)

... To understand the involvement of the antigens in the event of fertility as well as the cause of the infertility of male and female,the characterization of the sperm antigens and their antibodies that can be used in blocking these events are essential.The major goat sperm maturation antigen (SMA2) is ...
Multidrug Resistance-related protein cMOAT/MRP2, clone M2II-12
Multidrug Resistance-related protein cMOAT/MRP2, clone M2II-12

... Rev. 08/04 Cat.# MNS-MON9032 ...
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Bimolecular fluorescence complementation



Bimolecular fluorescence complementation (also known as BiFC) is a technology typically used to validate protein interactions. It is based on the association of fluorescent protein fragments that are attached to components of the same macromolecular complex. Proteins that are postulated to interact are fused to unfolded complementary fragments of a fluorescent reporter protein and expressed in live cells. Interaction of these proteins will bring the fluorescent fragments within proximity, allowing the reporter protein to reform in its native three-dimensional structure and emit its fluorescent signal. This fluorescent signal can be detected and located within the cell using an inverted fluorescence microscope that allows imaging of fluorescence in cells. In addition, the intensity of the fluorescence emitted is proportional to the strength of the interaction, with stronger levels of fluorescence indicating close or direct interactions and lower fluorescence levels suggesting interaction within a complex. Therefore, through the visualisation and analysis of the intensity and distribution of fluorescence in these cells, one can identify both the location and interaction partners of proteins of interest.
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