Why does Coomassie Brilliant Blue R interact differently with different proteins? A partial answer.
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Cloning of a cDNA coding for human factor V, a blood coagulation factor homologous to factor VIII and ceruloplasminThe organisation of Ebola virus reveals a capacity for extensive, modular polyploidyIntrinsically disordered and pliable Starmaker-like protein from medaka (Oryzias latipes) controls the formation of calcium carbonate crystalsSegmental Isotope Labelling of an Individual Bromodomain of a Tandem Domain BRD4 Using Sortase AMissense mutation Lys18Asn in dystrophin that triggers X-linked dilated cardiomyopathy decreases protein stability, increases protein unfolding, and perturbs protein structure, but does not affect protein function.Optimization of the Production Process and Characterization of the Yeast-Expressed SARS-CoV Recombinant Receptor-Binding Domain (RBD219-N1), a SARS Vaccine Candidate.Stepwise loss of fluorescent core protein V from human adenovirus during entry into cells.Mass spectrometry and next-generation sequencing reveal an abundant and rapidly evolving abalone sperm protein.Ribose sugars generate internal glycation cross-links in horse heart myoglobin.The outer dynein arm-docking complex: composition and characterization of a subunit (oda1) necessary for outer arm assemblyCdk2-dependent phosphorylation of p21 regulates the role of Cdk2 in cisplatin cytotoxicityISWI remodelling of physiological chromatin fibres acetylated at lysine 16 of histone H4.Digestion assays in allergenicity assessment of transgenic proteins.Lysine-Specific Demethylase 1A (KDM1A/LSD1): Product Recognition and Kinetic Analysis of Full-Length Histones.Apolipophorin III lysine modification: Effect on structure and lipid binding.Quantitative proteomics: assessing the spectrum of in-gel protein detection methods.Heterologous expression of moss light-harvesting complex stress-related 1 (LHCSR1), the chlorophyll a-xanthophyll pigment-protein complex catalyzing non-photochemical quenching, in Nicotiana sp.Reduction of cytotoxicity of benzalkonium chloride and octenidine by Brilliant Blue GUse of Nonspecific, Glutamic Acid-Free, Media and High Glycerol or High Amylase as Inducing Parameters for Screening Bacillus Isolates Having High Yield of Polyglutamic Acid.Systematical optimization of reverse-phase chromatography for shotgun proteomics.Membrane protein phosphotyrosine phosphatase in rabbit kidney. Proteolysis activates the enzyme and generates soluble catalytic fragments.Purification and characterization of a membrane protein (gp45-70) that is a cofactor for cleavage of C3b and C4b.Should digestion assays be used to estimate persistence of potential allergens in tests for safety of novel food proteins?An Albumin-binding Polypeptide Both Targets Cytotoxic T Lymphocyte Vaccines to Lymph Nodes and Boosts Vaccine Presentation by Dendritic Cells.DnaC, the indispensable companion of DnaB helicase, controls the accessibility of DnaB helicase by primase.Rapid and ultra-sensitive quantitation of disease-associated α-synuclein seeds in brain and cerebrospinal fluid by αSyn RT-QuIC.Subunit organization of a synechocystis hetero-oligomeric thylakoid FtsH complex involved in photosystem II repair.
P2860
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P2860
Why does Coomassie Brilliant Blue R interact differently with different proteins? A partial answer.
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1985 nî lūn-bûn
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1985年の論文
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1985年学术文章
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1985年学术文章
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1985年学术文章
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Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@en
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
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type
label
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@en
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@nl
prefLabel
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@en
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@nl
P2093
P1476
Why does Coomassie Brilliant B ...... nt proteins? A partial answer.
@en
P2093
P304
P407
P577
1985-08-01T00:00:00Z