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AB141085

Wiskostatin, N-WASP inhibitor

Wiskostatin, N-WASP inhibitor

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(6 Publications)

MW 426.1 Da, Purity >99%. Selective neural Wiskott-Aldrich syndrome protein (N-WASP) inhibitor. Binds the GTPase binding domain stabilising the autoinhibited conformation. Prevents activation of Arp2/3 complex in the actin cytoskeleton.

別名を表示する

AI413597, AW045860, DDPAC, FLJ31424, FTDP 17, G protein beta1/gamma2 subunit interacting factor 1, MAPT, MAPTL, MGC134287, MGC138549, MGC156663, MGC2124, MGC60244, MSTD, MTBT1, MTBT2, Microtubule associated protein tau isoform 4, Microtubule-associated protein tau, Mtapt, Neurofibrillary tangle protein, PHF-tau, PPND, PPP1R103, Paired helical filament-tau, Protein phosphatase 1, regulatory subunit 103, RGP 4, RGS4_HUMAN, RNPTAU, Regulator of G protein signalling 4, Regulator of G-protein signaling 4, SCZD 9, Schizophrenia disorder 9, TAU_HUMAN, Tauopathy and respiratory failure, Tauopathy and respiratory failure, included, pTau

1 Images
Chemical Structure - Wiskostatin, N-WASP inhibitor (AB141085)
  • Chemical Structure

Lab

Chemical Structure - Wiskostatin, N-WASP inhibitor (AB141085)

2D chemical structure image of ab141085, Wiskostatin, N-WASP inhibitor

Key facts

CAS番号

253449-04-6

精製度

>99%

製品の状態

Solid

form

分子量

426.1 Da

分子式

C<sub>1</sub><sub>7</sub>H<sub>1</sub><sub>8</sub>Br<sub>2</sub>N<sub>2</sub>O

PubChem

2775510

由来

Synthetic

溶解性

Soluble in DMSO to 100 mM

化学名

Wiskostatin

生物学的記述

Selective neural Wiskott-Aldrich syndrome protein (N-WASP) inhibitor. Binds the GTPase binding domain stabilising the autoinhibited conformation. Prevents activation of Arp2/3 complex in the actin cytoskeleton.

Canonical smiles

CN(C)CC(CN1C2=C(C=C(C=C2)Br)C3=C1C=CC(=C3)Br)O

InChi

InChI=1S/C17H18Br2N2O/c1-20(2)9-13(22)10-21-16-5-3-11(18)7-14(16)15-8-12(19)4-6-17(15)21/h3-8,13,22H,9-10H2,1-2H3

InChiKey

XUBJEDZHBUPBKL-UHFFFAOYSA-N

IUPAC名

1-(3,6-dibromocarbazol-9-yl)-3-(dimethylamino)propan-2-ol

出荷温度及び保存条件

出荷温度
Ambient - Can Ship with Ice
短期保存温度
+4°C
長期保存温度
+4°C
保管に関する情報
The product can be stored for up to 12 months

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Tau also known as MAPT (Microtubule-Associated Protein Tau) is a protein that primarily functions in stabilizing microtubules. It plays an essential role in ensuring proper neuronal cell shape and intracellular transport. Tau has several isoforms generated through alternate splicing each with a specific mass ranging from 45 to 68 kDa. This protein is abundantly found in neurons within the central nervous system although its presence has also been detected in other cell types but at much lower levels.
Biological function summary

Tau acts to stabilize microtubules which are structural components critical for maintaining neuronal morphology and function. It may also interact with actin filaments and other cytoskeletal proteins. Tau’s stabilization of microtubules is important for axonal transport a process that delivers essential nutrients and signaling molecules across cells. tau is often associated with complexes involving cytoskeletal elements and various microtubule-associated proteins.

Pathways

The role of Tau plays in cellular signaling and transport makes it an important component of pathways like the MAPK/ERK pathway and PI3K/AKT signaling. These pathways are involved in cell differentiation survival and proliferation. Other notable proteins that share these pathways include amyloid precursor protein (APP) and glycogen synthase kinase 3 beta (GSK-3β). Tau's hyperphosphorylation can disrupt these pathways adversely affecting neuronal health.

The aggregation and malfunction of Tau are intensely linked to Alzheimer's disease and frontotemporal dementia. Abnormal phosphorylation of Tau leads to the formation of neurofibrillary tangles a hallmark of Alzheimer's pathology. In these conditions Tau interacts with proteins such as amyloid-beta (Aβ) found in amyloid plaques. These pathologies highlight Tau’s role not just as a structural protein but as a critical factor in neurodegenerative processes.

製品プロトコール

文献 (6)

Recent publications for all applications. Explore the full list and refine your search

Cell structure and function 50:103-113 PubMed40058796

2025

Macropinocytosis regulates cytokine expression through Erk signaling in LPS-stimulated macrophages.

Applications

Unspecified application

Species

Unspecified reactive species

Li Wang,Yanan Li,Yuxin He,Yuchen Fang,Hitomi Mimuro,Adam C Midgley,Sei Yoshida

Cell stem cell 31:640-656.e8 PubMed38701758

2024

Lumen expansion is initially driven by apical actin polymerization followed by osmotic pressure in a human epiblast model.

Applications

Unspecified application

Species

Unspecified reactive species

Dhiraj Indana,Andrei Zakharov,Youngbin Lim,Alexander R Dunn,Nidhi Bhutani,Vivek B Shenoy,Ovijit Chaudhuri

Journal of cellular physiology 238:1063-1079 PubMed36924084

2023

Identification of circular dorsal ruffles as signal platforms for the AKT pathway in glomerular podocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Rui Hua,Jinzi Wei,Mauricio Torres,Yuxin He,Yanan Li,Xiaowei Sun,Li Wang,Ken Inoki,Sei Yoshida

Development (Cambridge, England) 149: PubMed36469048

2022

N-WASP-Arp2/3 signaling controls multiple steps of dendrite maturation in Purkinje cells in vivo.

Applications

Unspecified application

Species

Unspecified reactive species

Koichi Hasegawa,Takeshi K Matsui,Junpei Kondo,Ken-Ichiro Kuwako

Neuron 93:854-866.e4 PubMed28231467

2017

Synaptic Vesicle Endocytosis Occurs on Multiple Timescales and Is Mediated by Formin-Dependent Actin Assembly.

Applications

Unspecified application

Species

Unspecified reactive species

Tolga Soykan,Natalie Kaempf,Takeshi Sakaba,Dennis Vollweiter,Felix Goerdeler,Dmytro Puchkov,Natalia L Kononenko,Volker Haucke

Journal of cell science 127:1052-1064 PubMed24424029

2014

Podosomes of dendritic cells facilitate antigen sampling.

Applications

Unspecified application

Species

Unspecified reactive species

Maksim Baranov,Martin Ter Beest,Inge Reinieren-Beeren,Alessandra Cambi,Carl G Figdor,Geert van den Bogaart
View all publications

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