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Fundamentals of Biochemistry
Fundamentals of Biochemistry

... • Explain how an antibody could be useful for purifying a protein and for determining its concentration. • Describe the basis for separating proteins by ion exchange, hydrophobic interaction, gel filtration, and affinity chromatography. • Describe the processes of gel electrophoresis, SDS-PAGE, and ...
Determination of Protein Concentration
Determination of Protein Concentration

... and tryptophan, and thus the UV detection is highly sensitive to pH and ionic strength at which measurement is taken. Many other cellular components, and particularly nucleic acids, also absorb UV light. The ratio of A 280 /A 260 is often used as a criterion of the purity of protein or nucleic acid ...
File
File

... Many plant proteins are low in one of the essential amino acids (i.e, grains are short of lysine) – thus it is important for vegetarians to have a vast _______________ of vegetable and grain proteins. ...
Leukaemia Section del(11)(q23q23) MLL/ARHGEF12 Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section del(11)(q23q23) MLL/ARHGEF12 Atlas of Genetics and Cytogenetics in Oncology and Haematology

... domain: methyltransferase; methylates H3, including histones in the HOX area for allowing chromatin to be open to transcription. MLL is cleaved by taspase 1 into 2 proteins before entering the nucleus: a p300/320 Nterm protein called MLL-N, and a p180 C-term protein, called MLL-C. The FYRN and a FRY ...
Introduction
Introduction

... ubiquitin. To study the behaviour of ubiquitin in living cells, we fused the Green Fluorescent Protein (GFP) to the N-terminus of ubiquitin as was described before by Yewdell and Dantuma. In this system we are able to compare the ubiquitin and the ...
Leukaemia Section t(9;9)(q34;q34) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(9;9)(q34;q34) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... contains two leucine zipper dimerization domains, and FG repeats at the C-terminus, which are homologous to those observed in other members of the nucleoporin family; expressed in thymus, spleen, bone marrow, kidney, brain and testis, but hardly in all other tissues or in whole embryos during develo ...
File
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... Small Polar Molecules. ...
Whole Foods Production NS430
Whole Foods Production NS430

... grains, legumes, and leafy green vegetables.  Combine some incomplete proteins with complete ...
How to start to crystallise proteins
How to start to crystallise proteins

... How to start to crystallise proteins The sparse matrix design is probably the most common search strategy in use today for initial screening of crystallization conditions. Its popularity is due to its success and its ease of use, now that the formulations are available as commercial kits. Recent dat ...
投影片 1
投影片 1

... The fluorescence lifetime refers to the average time the molecule stays in its excited state before emitting a photon. Fluorescence typically follows first-order kinetics: where [S]t is the concentration of excited state molecules at time t, [S]0 is the initial concentration and Γ is the decay rate ...
CCND1 antibody - middle region (AVARP03037_P050)
CCND1 antibody - middle region (AVARP03037_P050)

... Rabbit Polyclonal Cyclin D1 This is a rabbit polyclonal antibody against CCND1. It was validated on Western Blot using a cell lysate as a positive control. Aviva Systems Biology strives to provide antibodies covering each member of a whole protein family of your interest. We also use our best effort ...
Health significance of protein
Health significance of protein

... amino acids (AAs) also play a role ...
Protein structure
Protein structure

... made up of such elements as carbon, hydrogen, nitrogen, phosphorus, oxygen, and sulfur. All proteins are polymers of amino acids. The polymers, also known as polypeptides consist of a sequence of 20 different L-α-amino acids, also referred to as residues. For chains under 40 residues the term peptid ...
PPT (without movies)
PPT (without movies)

... important scientific research. Join this free online game and help us predict the folds of unsolved proteins as well as designing new proteins to cure diseases. We’re collecting data to find out if humans' pattern-recognition and puzzle-solving abilities make them more efficient than existing comput ...
Module 5
Module 5

... (or motifs) common to homologous proteins. These motifs, usually of the order of 10-20 amino acids in length, usually correspond to key functional or structural elements, often domains, and are extremely useful in identifying such features in new uncharacterized proteins. There is a number of such s ...
Problem 2
Problem 2

... Finally, a -loop was indicated, and I had no idea what one of those was either. So here it is: ...
In this activity you will be translating the mRNA codons into the final
In this activity you will be translating the mRNA codons into the final

... representing a type of covalent bond called a disulfide bond.) 3. What do you think would happen to this protein if codon #7 changed to GGU? Would the protein still work? Why or why not? 4. What do you think would happen to this protein if codon #7 was instead changed to UGA? Would the protein still ...
Modelling proteomes
Modelling proteomes

... like Salmonella and ...
ACUTE PHASE PROTEIN CONCENTRATIONS IN PERITONEAL
ACUTE PHASE PROTEIN CONCENTRATIONS IN PERITONEAL

... fragilis, the concentrations of C-reactive protein increased after 4 HAI, then declined for the next two hours, and reached a second peak level by 48 HAI. Discussion: C-reactive protein binds directly to several microorganisms, degenerating cells and cell remnants, activates complement by the classi ...
Nerve activates contraction
Nerve activates contraction

... can cause HUGE changes… Hemoglobin - an important protein used by red blood cells to transport Oxygen throughout the body. It is 146 Amino Acids long!! BUT, If you replace Glutamic acid (AA) with Valine (AA) at the sixth position, the hemoglobin cannot fold correctly. ...
Poster presentations
Poster presentations

... (The list is open till september 14) (A printable MSWord version of this page) Aharonovsky Elik (University of Haifa) Protein sequence modules and their relation to closed loops. Akabayov Barak, Irit Sagi (Weizmann Institute) The metal ion in the RNA helicase DbpA acts as a single atom turnover swit ...
Attachment 3 Speakers(English version)
Attachment 3 Speakers(English version)

... circle amplification" (RCA) and "rolling circle transcription" (RCT), which are isothermal DNA/RNA amplification methods widely used in the literature. Also important were Kool's early and ongoing developments in DNA-templated chemistry, a field that is now practiced in many labs worldwide; Kool was ...
proteins
proteins

... Protein Folding and Processing ...
Protein Quality Matters
Protein Quality Matters

... • Topline results: After completing nine months of resistance training, all participants experienced increases in lean muscle mass. The gains for participants consuming whey protein (3.3 kg) were significantly greater than for participants consuming soy protein (1.8 kg), and the whey group had mo ...
Sonac introduces new natural products for aqua feed
Sonac introduces new natural products for aqua feed

... One of the essential nutrients for shrimps is cholesterol. Driven by the increasing scarcity of conventional sources of cholesterol, Sonac recently developed Phosterol. This hydrolyzed protein of animal origin is produced in accordance with all relevant EU regulations and is readily available from r ...
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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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