transparent sealing tape (Revvity)
Revvity is a verified supplier 
Revvity manufactures this product 
90
Structured Review
Revvity
transparent sealing tape
Transparent Sealing Tape, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/transparent+sealing+tape/Plateseal%2C+Permanent+Seal+for+Microplates%2C+100%2Fpk/pmc09564337-153-6-13
Average 90 stars, based on 10 article reviews
Transparent Sealing Tape, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/transparent+sealing+tape/Plateseal%2C+Permanent+Seal+for+Microplates%2C+100%2Fpk/pmc09564337-153-6-13
Average 90 stars, based on 10 article reviews
transparent sealing tape - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
other:Article Title: Conjugation of Short Peptides to Dibenzodiazepinone-Type Muscarinic Acetylcholine Receptor Ligands Determines M2R Selectivity Article Snippet: Muscarinic acetylcholine receptors (MRs), comprising five subtypes (M1R-M5R) in humans, exhibit a high degree of structural similarity.. Therefore, subtype-selective MR agonists and antagonists are lacking.. We present an approach to highly M2R-selective MR antagonists based on the conjugation of dior tripeptides to M2R-preferring dibenzodiazepinone-type MR antagonists. Article Title: Development of a Neurotensin-Derived 68 Ga-Labeled PET Ligand with High In Vivo Stability for Imaging of NTS 1 Receptor-Expressing Tumors Article Snippet: The plates were sealed with a Article Title: N(ω)-Carbamoylation of the Argininamide Moiety: An Avenue to Insurmountable NPY Y1 Receptor Antagonists and a Radiolabeled Selective High-Affinity Molecular Tool ([(3)H]UR-MK299) with Extended Residence Time. Article Snippet: Subscriber access provided by FLORIDA INTL UNIV Journal of Medicinal Chemistry is published by the American Chemical Society.. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society.. Copyright © American Chemical Society. Article Title: M2 Subtype preferring dibenzodiazepinone-type muscarinic receptor ligands: Effect of chemical homo-dimerization on orthosteric (and allosteric?) binding. Article Snippet: A series of new dibenzodiazepinone-type muscarinic receptor ligands, including two homo-dimeric compounds, was prepared.. Sixteen representative compounds were characterized in equilibrium binding studies with [H]N-methylscopolamine ([H]NMS) at the muscarinic receptor subtype M2, and seven selected compounds were additionally investigated at M1, M3, M4 and M5 with respect to receptor subtype selectivity.. The side chain of the known M2 preferring muscarinic receptor antagonist DIBA was widely varied with respect to chain length and type of the basic group (amine, imidazole, guanidine and piperazine). Article Title: Mimicking of Arginine by Functionalized Nω-Carbamoylated Arginine As a New Broadly Applicable Approach to Labeled Bioactive Peptides: High Affinity Angiotensin, Neuropeptide Y, Neuropeptide FF, and Neurotensin Receptor Ligands As Examples Article Snippet: Derivatization of biologically active peptides by conjugation with fluorophores or radionuclide-bearing moieties is an effective and commonly used approach to prepare molecular tools and diagnostic agents.. Whereas lysine, cysteine, and N-terminal amino acids have been mostly used for peptide conjugation, we describe a new, widely applicable approach to peptide conjugation based on the nonclassical bioisosteric replacement of the guanidine group in arginine by a functionalized carbamoylguanidine moiety.. Four arginine-containing peptide receptor ligands (angiotensin II, neurotensin(8−13), an analogue of the C-terminal pentapeptide of neuropeptide Y, and a neuropeptide FF analogue) were subject of this proof-of-concept study. Radioactivity:Article Title: Radiolabeled Dibenzodiazepinone-Type Antagonists Give Evidence of Dualsteric Binding at the M2 Muscarinic Acetylcholine Receptor Article Snippet: The dualsteric ligand approach, aiming at ligands with improved subtype selectivity, has been increasingly applied to muscarinic receptors (MRs).. In this article we present the synthesis and characterization of a M2R subtype-preferring radiolabeled dibenzodiazepinone-type antagonist ([H]UNSW-MK259, [H]19) and its homodimeric analog [H]UR-AP060, ([H]33).. Saturation binding studies at the M2R, using the orthosteric antagonist atropine to determine unspecific binding, proved that the monomeric and the dimeric compound bind to the orthosteric binding site (apparent Kd: 0.87 and 0.24 nM, respectively). |