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The variable and conserved interfaces of modeled olfactory receptor
The variable and conserved interfaces of modeled olfactory receptor

... An important question is whether some or all the variable OR residues may line the putative ligand-binding interface. Such interfaces are known to be located in the barrel interior in other ...
GABA RECEPTORS GABA RECEPTORS
GABA RECEPTORS GABA RECEPTORS

... GABA is the major inhibitory amino acid transmitter of the mammalian central nervous system and it is present in some 40% of all neurones. Most of the early studies, carried out with iontophoretic application of GABA in the CNS, indicated that it generally produced inhibitory hyperpolarizing respons ...
Document
Document

... responses at 10- to 100-fold lower levels than dust mite and cat allergens.6,7 Despite sharing sequence homology with the aspartic proteinase family of proteolytic enzymes, Bla g 2 lacked proteolytic activity in a standard milk-clotting assay that used casein as a substrate.8 A molecular model of Bl ...
Allosteric Inhibition of Aminoglycoside Phosphotransferase by a
Allosteric Inhibition of Aminoglycoside Phosphotransferase by a

... To obtain crystals of APH in complex with the selected AR protein inhibitor, AR_3a, a mutant APH (mAPH) was created in which the two surface cysteine residues (C19, C156) of APH were replaced by serine. In wildtype APH (wtAPH), both cysteines can form intermolecular C19-C156 disulfide bonds, which m ...
Combinatorial Chemistry and High Throughput Screening
Combinatorial Chemistry and High Throughput Screening

... blocks in each well depends on the sequence of the target peptide on the pin it Corresponds to. ...
Structural Characterization of Humanized Nanobodies with
Structural Characterization of Humanized Nanobodies with

... structure-stabilizing bridge in a β-roll structure within each RTX-Block region [10–12]. Moreover, CyaA is synthesized as an inactive precursor which requires a palmitoyl group be added at Lys983 by CyaC acyltransferase [7,13,14]. The CyaA-RTX subdomain is involved in toxin binding to target cells t ...
OptCDR: a general computational method for the design
OptCDR: a general computational method for the design

... majority of antibody-binding interactions. Humanization (Almagro and Fransson, 2008) is a common experimental technique where the CDRs from a non-human antibody are attached to the framework of a human antibody, thereby retaining the binding properties of the non-human antibody while decreasing or e ...
Model Description Sheet
Model Description Sheet

... population, especially poor, developing countries, as it kills approximately 2 million people each year according to the World Health Organization. Because of overuse and increasing resistance to current antibiotics, researchers are working to develop new drugs to more effectively treat tuberculosis ...
CUCURBIT[7]URIL HOST-GUEST COMPLEXES WITH DRUG MOLECULES CONTAINING ISOQUINOLINE GROUPS Julian Kwok by
CUCURBIT[7]URIL HOST-GUEST COMPLEXES WITH DRUG MOLECULES CONTAINING ISOQUINOLINE GROUPS Julian Kwok by

... the polymethylene chain length is between six and ten carbons, or is replaced with a pxylyl group, the first CB[7] will bind over the central bridge, resulting in both of the polar portals forming ion-dipole interactions with both positively charged nitrogens. A second CB[7] binds to a terminal isoq ...
Comparative Models of GABAA Receptor
Comparative Models of GABAA Receptor

... Fig. 1. Alignment of nACh and GABAA receptor helical domains. a, a subset of a superfamily alignment of the four segments that make up the helical (transmembrane) domain of the subunit chains is shown. The position of the missing “cytoplasmic loop” between helices 3 and 4 is indicated by a double-ga ...
A Chemical Approach To Illustrate the Principal of Signal
A Chemical Approach To Illustrate the Principal of Signal

... for signal transduction. Generally, the sequential process is initiated by the binding of an extracellular signal to a receptor culminating in one or more specific cellular responses In this way, a signal, for example, can be transferred from the outside of the cell en route to the nucleus—a process ...
Structure and Gas-Phase Stability of Zn(II)—Molecule Complexes
Structure and Gas-Phase Stability of Zn(II)—Molecule Complexes

... in the majority of these enzymes zinc cation Zn2+ is directly involved in the catalytic mechanism [1]. It has been shown that presence of a potent Zn2+ binding functional group in the molecule of inhibitor may significantly influence the overall binding affinity to the enzyme active site (e.g. up to 60 ...
Pore-Exposed Tyrosine Residues of P
Pore-Exposed Tyrosine Residues of P

... pH 7.8, containing rh123 (Sigma-Aldrich) at a final concentration of 0.2 mg/ml (0.53 mM) and incubated at 37°C under gentle continuous agitation for 30 minutes. Loading was terminated by chilling tubes on ice and cells were washed twice with ice-cold DMEM, pH 7.4. Efflux was initiated by resuspendin ...
Stereo Isomerism
Stereo Isomerism

...  If rotation was counterclockwise = Λ  If rotation was clockwise = Δ ...
Enzymes
Enzymes

... High sensitivity and precision For purification, specific activities of most enzymes are very low. Therefore, the assay must be highly sensitive. The accuracy and precision of an enzyme assay usually depend on the underlying chemical basis of techniques that are used. For example, if an assay is ca ...
O A RIGINAL RTICLE
O A RIGINAL RTICLE

... virtual screen or performing a ROCS-based alignment for design always involve choosing a reference or bioactive conformation [17-23]. Finding good reference conformations for virtual screening is not always easy to do, especially for a diverse set of ligands. In this case, multiple queries or refere ...
Kinetic analysis of cooperativity of phosphorylated L
Kinetic analysis of cooperativity of phosphorylated L

... calculated from Eq. (10). As the simultaneous influence of both substrates on the reaction rate was taken into account by this model, these parameters do not depend on the concentration of either of the two substrates. Therefore the constant K A should explicitly characterize the interaction of ADP ...
N Goalby chemrevise.org 1 2.5 Transition Metals Substitution
N Goalby chemrevise.org 1 2.5 Transition Metals Substitution

... This chelate effect can be explained in terms of a positive entropy change in these reactions as more molecules of products than reactants [Cu(H2O)6]2+ (aq) + EDTA4- (aq)  [Cu (EDTA)]2- (aq) + 6H2O (l) The copper complex ion has changed from having unidentate ligands to a multidentate ligand. In th ...
Modifications of a Nanomolar Cyclic Peptide
Modifications of a Nanomolar Cyclic Peptide

... extracellular ligand-binding domain (LBD) of EphA4 are available.2 Peptides appear to have greater potential than small molecules (such as rhynchophylline and bile acid derivatives) for high affinity, selective binding to the ephrinbinding pocket of EphA4 due to its broad surface and conformational fle ...
Åpne - Munin
Åpne - Munin

... accumulate in the environment and evidence suggests that most people have varying degrees of toxic compounds within their body. This can result in disruption of many physiological processes in the human body and the development of several central nervous system (CNS) diseases, including Alzheimer’s ...
Succinyl-CoA Synthetase Activity Colorimetric Assay Kit
Succinyl-CoA Synthetase Activity Colorimetric Assay Kit

... Succinyl-CoA Synthetase (SCS, also called Succinyl-CoA ligase, Succinate Thiokinase) (EC 6.2.1.5) is a critical enzyme in the citric acid cycle and an important metabolic intermediate for porphyrin, heme and ketone body biosynthesis. It is located in the mitochondrial matrix and is a heterodimer com ...
Mitochondrial permeability transition pore
Mitochondrial permeability transition pore

... X ...
Sign of enthalpy changes Exothermic vs endothermic Acid
Sign of enthalpy changes Exothermic vs endothermic Acid

... • Molar Hm = Cp,m T • Total H = Cp T = nCp,m p m T • Specific heat capacity (Cp per unit mass) may be useful. WHAT IS IT FOR H2O? • Calculation assumes that Cp is not changing within the temp. range of the experiment. • T = H/(nC H/(n Cp,m) • Cp,m= H/(nT) ...
Neurotransmitter Systems
Neurotransmitter Systems

... Studying Neurotransmitter Systems Localization of Transmitters and their Synthesis Enzymes Whatever the inspiration, the first step in confirming the hypothesis on a new neurotransmitter is to show that the molecule is, in fact, localized in, and synthesized by, particular neurons. Many methods h ...
NICKEL(II) PINCER COMPLEXES SUPPORTED BY 2,6
NICKEL(II) PINCER COMPLEXES SUPPORTED BY 2,6

... The starting material of the ligand synthesis, 2,6-dicarboxaldehye was prepared from 2,6-dimethanol pyridine through oxidation with SeO2/Dioxane (Figure 9). Then, tolualdehyde was stirred at room temperature for 5 h with 4-methylacetophenone and NaOH in EtOH/H2O to form 1,3-bis(4-tolyl)-2-propen-1-o ...
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Ligand binding assay

Ligand Binding Assays (LBA) is an assay, or an analytic procedure, whose procedure or method relies on the binding of ligand molecules to receptors, antibodies or other macromolecules. A detection method is used to determine the presence and extent of the ligand-receptor complexes formed, and this is usually determined electrochemically or through a fluourescence method. This type of analytic test can be used to test for the presence of target molecules in a sample that are known to bind to the receptor.There are numerous types of ligand binding assays, both radioactive and non-radioactive. As such, ligand binding assays are a superset of radiobinding assays, which are the conceptual inverse of radioimmunoassays (RIA). Some newer types are called ""mix-and-measure"" assays because they do not require separation of bound ligands.Ligand binding assays are used primarily in pharmacology for various demands. Specifically, despite the human body’s endogenous receptors, hormones, and other neurotransmitters, pharmacologists utilize assays in order to create drugs that are selective, or mimic, the endogenously found cellular components. On the other hand, such techniques are also available to create receptor antagonists in order to prevent further cascades. Such advances provide researchers with the ability not only to quantify hormones and hormone receptors, but also to contribute important pharmacological information in drug development and treatment plans.
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