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Ultraviolet-Visible Spectroscopy
Ultraviolet-Visible Spectroscopy

...  Scatter in solution Large molecules Air bubbles • Normalized by comparison to reference cell  Contains only solvent Measurement for transmittance is compared to results from reference cell ...
1 Biochemistry 462a – Hemoglobin Structure and Function Reading
1 Biochemistry 462a – Hemoglobin Structure and Function Reading

... 3. The presence of BPG aids the delivery of O2 by favoring the deoxy conformation. 4. Deoxy Hb binds CO2. 5. The deoxy Hb returns to the lungs where the pH is higher, the O2 content higher and the CO2 content is lower. All these factors favor reverse of carbamate formation (loss of bound CO2), depro ...
2-7 Active-Site Geometry
2-7 Active-Site Geometry

... orientation and the collision will be non-productive. Thus, if both molecules first bind to an enzyme active site, and do so in such a way that their reactive portions are juxtaposed, the probability of a reaction is optimized. In solution, when two molecules collide but do not react they bounce off ...
1 From Chemical Invariance to Genetic Variability - Wiley-VCH
1 From Chemical Invariance to Genetic Variability - Wiley-VCH

... Next we note that evolutionary variability is not uniform throughout the structure of a metalloenzyme. Variability increases and invariance decreases from the (innermost) transition metal through the (inner) ligators to the (outer) ligand moieties. Hence, in the course of evolution central transitio ...
Complex Formation Between Iron(III) and
Complex Formation Between Iron(III) and

... The pKa value for the ligand was determined spectrophotometrically by the method of Albert and Sergent (1971) using boric acid and borax of ionic strength 0.1 mol dm-3 and 0.025 mol dm-3 as buffer for INHA ligand. In each case, the ligand stock solution was 5.0 x 10-4 mol dm-3 diluted five folds in ...
Caffeoylquinic acids as inhibitors for HIV-I protease and HIV
Caffeoylquinic acids as inhibitors for HIV-I protease and HIV

... Three types of docking were used on this study. In rigid docking, the possible binding conformations of a ligand (small molecule) in a specific area of the receptor are evaluated by rotating its bonds and translating the molecule. Flexible docking is similar to rigid docking in the sense that the se ...
Caffeoylquinic acids as inhibitors for HIV-I protease and HIV
Caffeoylquinic acids as inhibitors for HIV-I protease and HIV

... Three types of docking were used on this study. In rigid docking, the possible binding conformations of a ligand (small molecule) in a specific area of the receptor are evaluated by rotating its bonds and translating the molecule. Flexible docking is similar to rigid docking in the sense that the se ...
Gene Section IGFBP6 (insulin-like growth factor binding protein 6)
Gene Section IGFBP6 (insulin-like growth factor binding protein 6)

... binding preference for IGF-II over IGF-I. It therefore is a relatively specific inhibitor of IGF-II actions (Bach, 1999; Bach, 2005; Bach et al., 2013). It is antiproliferative and proapoptotic in a number of cell lines in vitro (Bach, 1999; Bach, 2005; Bach et al., 2013). At least some of its actio ...
Reading - Chapter 15 and the Appendix to Chapter 15
Reading - Chapter 15 and the Appendix to Chapter 15

... The differences in O2 affinity between T-State (deoxy) and R-State (oxy) Hb can be understood in terms of the changes in quaternary structure that accompany the conversion of deoxy Hb to oxy Hb. o The shift from the deoxy to oxy conformation arises from the fact that in deoxy Hb the iron lies out of ...
Transition
Transition

... • Two catalytic modes based on binding properties can each increase reaction rates over 10,000-fold : (1) Proximity effect - collecting and positioning substrate molecules in the active site ...
DOPAMINE RECEPTORS
DOPAMINE RECEPTORS

... • Role in pleasure and motivation • Controls the flow of information from other areas of the brain ...
Analysis of Cell Ageing
Analysis of Cell Ageing

... Ligands bind to receptors which directly bind to specific regions of the genome which regulate the transcription of specific genes. The receptors have 3 regions – N terminus which is a transcription activating domain, then a DNA binding domain and a hormone binding at the C terminus. The hormone bin ...
Relationship between the structure and function of proteins
Relationship between the structure and function of proteins

... • When Hb is oxygenated it ionizes to free one H+ for each O2 bound as seen in the equation. • Since the reaction is a reversible reaction , increasing the [ H+ ] will cause the equilibrium to shift to the left releasing the O2 . • The relationship between pH and the Hb %Oxygen saturation is directl ...
Structure-function of the ADP/ATP carrier
Structure-function of the ADP/ATP carrier

... the cytosolic side by use of peptide-directed aritibodies [ 3 ] .It remains controversial whether there is an even or uneven nurnber of transmembrane segments. No direct evidence for the location of the Cterminus of the AAC has been produced so far. I Iowever, in the similar uncoupling protein o f b ...
Our work was originally motivated my collaboration with Drs
Our work was originally motivated my collaboration with Drs

... a phage virion, while the genetic material encoding each variant resides on the inside (1-3). This creates a physical linkage between each variant protein sequence and the DNA encoding it, which allows rapid partitioning based on binding affinity to a given target molecule (antibodies, enzymes, cell ...
Topic 4 Proteins as Drug Targets
Topic 4 Proteins as Drug Targets

... • Many common receptors belong to this same family • Implications for drug selectivity depending on similarity (evolution) • Membrane bound receptors difficult to crystallise • X-Ray structure of bacteriorhodopsin solved - bacterial protein similar to rhodopsin • Bacteriorhodopsin structure used as ...
High resolution crystal structures of unliganded
High resolution crystal structures of unliganded

... model, provided that they were not close to the putative ligand molecules or Zn2þ ions. Three 30 -phosphate-AMP moieties of the ligand molecules had clear continuous density in the initial (Fo # Fc) ac maps and these fragments were added in the model (molecules C1, D1, and P1; C1 is bound to monomer ...
Lecture PPT - Carol Eunmi LEE
Lecture PPT - Carol Eunmi LEE

... mineralocorticoid receptor evolved by a stepwise selective process • Ancestral gene resurrection demonstrates that long before the hormone evolved, the receptor’s affinity for aldosterone was present due to its similarity to more ancient ligands (probably DOC) – also, ancestral receptor was less spe ...
Practice Exam II
Practice Exam II

... a). The difference in Gibbs free energy between the reactant and product before catalysis. b). The difference in Gibbs free energy between the reactant and product after catalysis. c). The difference in Gibbs free energy between an enzyme in the active (R-state) and inactive (T-state) ...
Practice Exam II answers
Practice Exam II answers

... : (c), Release of Pi causes an increase in the binding affinity of myosin to actin, and allows for the power stroke of muscle contraction. 25). What result on Hb would you expect in the mutation of E87  Y in the heme pocket, where Y now interacts with the heme iron? a). Fe3+ would be stabilized. b ...
to find the lecture notes for lecture 5 cellular communication click here
to find the lecture notes for lecture 5 cellular communication click here

... called kinases – kinases act to phosphorylate their targets – either activating them or inhibiting them – this speeds up/slows down physiological responses within the cell – phosphodiesterase inactivates cAMP quickly many second messengers are made in cells in response to specific hormones ...
Gwy-Am Shin
Gwy-Am Shin

... IMS (Immunomagnetic separation) ...
Document
Document

... specific selectivity and affinity to different inorganics. This database can be analysed for atom-atom preferences, torsion angle preferences, and other characteristics to define energy functions and move sets for performing protein structure simulations. We will combine this with our all-atom energ ...
Splice variant - Journal of Pharmacology and Experimental
Splice variant - Journal of Pharmacology and Experimental

... [3H]GABA uptake assay and FLIPR® membrane potential assay in mammalian cells transiently expressing the human GATs Cell culture and transfections – tsA201 cells (a transformed HEK293 cell line) were cultured in GlutaMAX-I DMEM supplemented with 10% fetal bovine serum, penicillin (100 U/mL), and str ...
immuno 2015 - hippocampus
immuno 2015 - hippocampus

... method. Include the protocol, information about the antibodies and their concentrations, the microscope, filter sets, and image acquisition program, as well as any programs used to process your images. Results: Describe the pattern of immunoreactivity. You should print out copies of your images to i ...
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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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