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AB142228

AEC (3-Amino-9-ethylcarbazole),Peroxidase底物

AEC (3-Amino-9-ethylcarbazole), Peroxidase substrate

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(1 Publication)

AEC (ab142228 ) is a red chromogen supplied as 50X concentrate (0.095 mol/l). Used in peroxidase detection in immunoblotting and IHC applications. Molecular weight (MW) 210.27.

- Compatible with AEC Substrate Buffer (ab286857)

查看别名

AHR_HUMAN, Ah receptor, Aromatic hydrocarbon receptor, Aryl hydrocarbon receptor, Aryl hydrocarbon receptor precursor, Class E basic helix-loop-helix protein 76, HGNC:348, bHLHe76

1 Images
Chemical Structure - AEC (3-Amino-9-ethylcarbazole), Peroxidase substrate (AB142228)
  • Chemical Structure

Lab

Chemical Structure - AEC (3-Amino-9-ethylcarbazole), Peroxidase substrate (AB142228)

2D chemical structure image of ab142228, AEC (3-Amino-9-ethylcarbazole), Peroxidase substrate

关键信息

CAS 号

132-32-1

形式

Liquid

form

分子量

210.27 Da

分子式

C<sub>1</sub><sub>4</sub>H<sub>1</sub><sub>4</sub>N<sub>2</sub>

PubChem

8588

属性

Synthetic

生化试剂名称

3-Amino-9-ethylcarbazole

生物学描述

Peroxidase substrate. Insoluble, red chromogen used for antibody detection in immunohistochemistry supplied as a 50X concentrate (0.095 mol/l).

经典 SMILES

CCN1C2=C(C=C(C=C2)N)C3=CC=CC=C31

InChi

InChI=1S/C14H14N2/c1-2-16-13-6-4-3-5-11(13)12-9-10(15)7-8-14(12)16/h3-9H,2,15H2,1H3

InChiKey

OXEUETBFKVCRNP-UHFFFAOYSA-N

IUPAC 名

9-ethylcarbazol-3-amine

产品详情

This product is manufactured by BioVision, an Abcam company and was previously called 2122 AEC. 2122-10 is the same size as the 10 ML size of ab142228.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

性能和储存信息

运输条件
Ambient - Can Ship with Ice
推荐的短期储存条件
+4°C
推荐的长期储存条件
+4°C
储存信息
The product can be stored for up to 12 months

补充信息

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

The Aryl hydrocarbon Receptor (AhR) also known as the Ah receptor is a ligand-activated transcription factor expressed in various tissues including liver lung and skin. The AhR has a molecular mass of approximately 96 kDa. It forms a complex with the aryl hydrocarbon receptor nuclear translocator (ARNT) upon ligand binding. AhR can bind to several compounds including aryl azide influencing the expression of numerous genes involved in xenobiotic metabolism.
Biological function summary

The AhR plays an important role in the regulation of detoxification enzymes such as cytochrome P450s. This receptor functions as a sensor for environmental toxins activating detoxification pathways once bound to ligands. It also contributes to the modulation of immune responses and development processes. The AhR often forms part of a larger protein complex to exert its effects on gene expression and cellular processes.

Pathways

The AhR significantly participates in the xenobiotic metabolism pathway and the dioxin signaling pathway. It interacts with proteins such as ARNT and cytochrome P450 enzymes to mediate the cellular response to toxins. The activity of AhR regulates the expression of phase I and phase II detoxification enzymes making it an integral part of the body’s defense against environmental chemicals.

Disturbances in AhR activity have been linked to cancer and autoimmune diseases. Altered expression or function of AhR can contribute to aberrant cell proliferation and immune dysregulation. The AhR interacts with other proteins like peroxidase and its substrates playing a role in oxidative stress responses associated with these conditions. Understanding these links can offer insights into therapeutic targets for related diseases.

产品实验方案

文献 (1)

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

Current eye research 44:590-598 PubMed30803276

2019

Efficacy of Sunitinib, Sunitinib-Hesperetin, and Sunitinib-Doxycycline Combinations on Experimentally-Induced Corneal Neovascularization.

Applications

Unspecified application

Species

Unspecified reactive species

Yeliz Ekim,Selcuk Kara,Baran Gencer,Turan Karaca
View all publications

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