Review of: Anillin

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Anillin

Anillin Antikörper (B) ist ein monoklonaler Anti-Anillin Antikörper, der m, r, und h Anillin in WB, IP, IF, IHC(P) und ELISA detektiert. Zitiert in 4 Publikationen. Contact Us to find out if we offer a single gene analysis for this gene. Genetic Testing. Skip navigation · Single Gene Analysis · Gene Panel Sequencing · Exome. Alternative Names, Scra,Scraps,Actin-Binding Protein Anillin. Sensitivity, pg/​mL. Sample Type, tissue homogenates, cell lysates and other biological fluids.

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Anillin is a highly conserved multidomain protein that crosslinks multiple structural and regulatory elements including, but not limited to, F-actin, active myosin II. Contact Us to find out if we offer a single gene analysis for this gene. Genetic Testing. Skip navigation · Single Gene Analysis · Gene Panel Sequencing · Exome. ANLN - anillin actin binding protein. Synonym(e): ANILLIN, scra, Scraps; Veraltete Symbole und Gennamen: anillin (Drosophila Scraps homolog), actin binding.

Anillin Inhaltsverzeichnis Video

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View protein in InterPro IPR, AHD IPR, Anillin_N IPR, PH-like_dom_sf IPR, PH_Anillin IPR, PH_domain: Pfam i: View protein in Pfam PF, Anillin, 1 hit PF, Anillin_N, 2 hits PF, PH, 1 hit: SMART i.

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ANLN Reaktivität: Human ELISA, IHC p Wirt: Kaninchen Polyclonal. Diese Cookies werden von Webservices generiert, die Informationen über das Nutzerverhalten liefern, personalisierte Inhalte ausgeben oder den Werbeerfolg messen. Kategorie : Protein. MPMID Gene3D i. DMDM i. Addison Riecke curated single-nucleotide variation and disease association database More Nat Rev Mol Cell Biol. Phase behaviour solid—liquid—gas.

Doch ganz verzichten Kate Miner Anime-Fans zumindest im Juli nicht Anillin das Anime-Programm am Freitag: Am 5. - Gene Panel Sequencing

MPMID Anillin ist ein Protein aus Tieren, das am Zellwachstum und an der Zytokinese beteiligt ist. Es ist nicht zu verwechseln mit dem Aminobenzol Anilin. ANLN - anillin actin binding protein. Synonym(e): ANILLIN, scra, Scraps; Veraltete Symbole und Gennamen: anillin (Drosophila Scraps homolog), actin binding. Anillin is a highly conserved multidomain protein that crosslinks multiple structural and regulatory elements including, but not limited to, F-actin, active myosin II. Anillin ist ein Gen, das durch das Symbol ANLN kodiert wird. Es ist auch bekannt als ANLN. Anillin hat eine Masse von kDa, eine Aminosäurelänge von.

Consistent with these factors, substituted anilines with electron donating groups are more pyramidalized, while those with electron withdrawing groups are more planar.

The pyramidalization angle between the C—N bond and the bisector of the H—N—H angle is Industrial aniline production involves two steps. The reduction of nitrobenzene to aniline was first performed by Nikolay Zinin in , using inorganic sulfide as a reductant Zinin reaction.

Aniline can alternatively be prepared from ammonia and phenol derived from the cumene process. Many analogues of aniline are known where the phenyl group is further substituted.

These include toluidines , xylidines , chloroanilines , aminobenzoic acids , nitroanilines , and many others. They often are prepared by nitration of the substituted aromatic compounds followed by reduction.

For example, this approach is used to convert toluene into toluidines and chlorobenzene into 4-chloroaniline. The chemistry of aniline is rich because the compound has been cheaply available for many years.

Below are some classes of its reactions. The oxidation of aniline has been heavily investigated, and can result in reactions localized at nitrogen or more commonly results in the formation of new C-N bonds.

In alkaline solution, azobenzene results, whereas arsenic acid produces the violet-coloring matter violaniline. Chromic acid converts it into quinone , whereas chlorates , in the presence of certain metallic salts especially of vanadium , give aniline black.

Hydrochloric acid and potassium chlorate give chloranil. Potassium permanganate in neutral solution oxidizes it to nitrobenzene ; in alkaline solution to azobenzene , ammonia, and oxalic acid ; in acid solution to aniline black.

Hypochlorous acid gives 4-aminophenol and para-amino diphenylamine. These polymers exhibit rich redox and acid-base properties.

Like phenols , aniline derivatives are highly susceptible to electrophilic substitution reactions. Its high reactivity reflects that it is an enamine , which enhances the electron-donating ability of the ring.

If bromine water is added to aniline, the bromine water is decolourised and a white precipitate of 2,4,6-tribromoaniline is formed.

To generate the mono-substituted product, a protection with acetyl chloride is required:. The reaction to form 4-bromoaniline is to protect the amine with acetyl chloride, then hydrolyse back to reform aniline.

The largest scale industrial reaction of aniline involves its alkylation with formaldehyde. An idealized equation is shown:. The resulting diamine is the precursor to 4,4'-MDI and related diisocyanates.

Aniline is a weak base. Aromatic amines such as aniline are, in general, much weaker bases than aliphatic amines. Traditionally, the weak basicity of aniline is attributed to a combination of inductive effect from the more electronegative sp 2 carbon and resonance effects, as the lone pair on the nitrogen is partially delocalized into the pi system of the benzene ring.

Missing in such an analysis is consideration of solvation. Aniline is, for example, more basic than ammonia in the gas phase, but ten thousand times less so in aqueous solution.

Aniline reacts with acyl chlorides such as acetyl chloride to give amides. The amides formed from aniline are sometimes called anilides , for example CH 3 -CO-NH-C 6 H 5 is acetanilide.

At high temperatures aniline and carboxylic acids react to give the anilides. N -Methylation of aniline with methanol at elevated temperatures over acid catalysts gives N -methylaniline and dimethylaniline :.

These derivatives are of importance in the color industry. Aniline combines directly with alkyl iodides to form secondary and tertiary amines.

Aniline and its ring-substituted derivatives react with nitrous acid to form diazonium salts. Through these intermediates, aniline can be conveniently converted to -OH, -CN, or a halide via Sandmeyer reactions.

This diazonium salt can also be reacted with NaNO 2 and phenol to produce a dye known as benzeneazophenol, in a process called coupling. The reaction of converting primary aromatic amine into diazonium salt is called diazotisation.

In this reaction primary aromatic amine reacts with sodium nitrile and with 2 moles of HCl which is known as Ice cold mixture because the temperature use to be 0.

It reacts with nitrobenzene to produce phenazine in the Wohl-Aue reaction. Hydrogenation gives cyclohexylamine. Being a standard reagent in laboratories, aniline is used for many niche reactions.

Its acetate is used in the aniline acetate test for carbohydrates, identifying pentoses by conversion to furfural. It is used to stain neural RNA blue in the Nissl stain.

The largest application of aniline is for the preparation of methylenedianiline and related compounds by condensation with formaldehyde.

Endeavor, Volume 17, Issue 3. Consultado el 15 de mayo de Consultado el 24 de mayo de Consultado el 16 de mayo de Datos: Q Multimedia: Aniline.

The underlying mechanism is poorly understood. It has been suggested that incomplete disassembly of contractile elements prohibits cytokinesis.

Here, we show that serum-induced binucleation results in the normal disassembly of the contractile apparatus. Gene3D i 2. The information is filed in different subsections.

Show all Align All Q8K [ UniParc ] FASTA Add to basket Added to basket. Length: 1, Mass Da : , It is useful for tracking sequence updates. The algorithm is described in the ISO standard.

The sequence AAH differs from that shown. Reason: Erroneous initiation. The sequence BAC differs from that shown. Full view.

Protein Similar proteins Species Score Length Source Q8K Anillin HUMAN. These are stable identifiers and should be used to cite UniProtKB entries.

Upon integration into UniProtKB, each entry is assigned a unique accession number, which is called 'Primary citable accession number'.

UniProt is an ELIXIR core data resource. Main funding by: National Institutes of Health The European Molecular Biology Laboratory State Secretariat for Education, Research and Innovation SERI.

Do not show this banner again. Cell cycle , Cell division , Mitosis. Recommended name: Anillin. Four distinct tokens exist: 'Name', 'Synonyms', 'Ordered locus names' and 'ORF names'.

This is known as the 'taxonomic identifier' or 'taxid'. It lists the nodes as they appear top-down in the taxonomic tree, with the more general grouping listed first.

Mouse genome database MGD from Mouse Genome Informatics MGI More MGI i. Anillin Add BLAST. Phosphoserine Combined sources Manual assertion inferred from combination of experimental and computational evidence i Ref.

Phosphothreonine Combined sources Manual assertion inferred from combination of experimental and computational evidence i Ref.

Phosphotyrosine Combined sources Manual assertion inferred from combination of experimental and computational evidence i Ref.

Encyclopedia of Proteome Dynamics More EPD i. MaxQB - The MaxQuant DataBase More MaxQB i. PaxDb, a database of protein abundance averages across all three domains of life More PaxDb i.

PeptideAtlas More PeptideAtlas i. PRoteomics IDEntifications database More PRIDE i. GlyConnect protein glycosylation platform More GlyConnect i.

GlyGen: Computational and Informatics Resources for Glycoscience More GlyGen i. PhosphoSitePlus i. SwissPalm database of S-palmitoylation events More

Anillin High nuclear expression of anillin (ANLN) is an independent predictor of poor disease-specific survival and it is a useful prognostic marker of urothelial carcinoma of the upper urinary tract (UCUT). Data suggest that anillin (ANLN) could be involved in breast cancer progression and a potential target candidate in breast cancer. Overexpression of RC mutant ANLN in immortalized human podocytes results in enhanced podocyte motility. The mutant anillin displays reduced binding to the slit diaphragm-associated scaffold protein CD2AP. Anillin is a conserved protein implicated in cytoskeletal dynamics during cellularization and cytokinesis. The ANLN gene in humans and the scraps gene in Drosophila encode Anillin. In , anillin was first isolated in embryos of Drosophila melanogaster. It was identified as an F-actin binding protein. Aniline | C6H5NH2 or C6H7N | CID - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities. View protein in InterPro IPR, AHD IPR, Anillin_N IPR, PH-like_dom_sf IPR, PH_Anillin IPR, PH_domain: Pfam i: View protein in Pfam PF, Anillin, 1 hit PF, Anillin_N, 2 hits PF, PH, 1 hit: SMART i. Show all Align All. IntAct i. Abgesehen von den Naphtholen können auch andere Kupplungsreagenzien wie zum Beispiel 1-Naphthylamin eingesetzt werden. ProtoNet i. ANI-1 and ANI-2 proteins homologous to anillin are essential for embryonic viability in both organisms. IUPAC Benzolamin Aminobenzol Phenylamin. Bgee dataBase The Avengers Besetzung Gene Expression Anillin More The Xhamster Hotel CDS CCDS project More The AH domain of human anillin is essential for its interaction with RhoA. Unter Beibehaltung der beiden Stickstoffatome lässt sich das Benzoldiazoniumion zum Beispiel mit Natriumsulfit in wässriger Lösung zum Phenylhydrazin reduzieren:.

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