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Key Documents

AB9726

Sigma-Aldrich

Anti-Serotonin Transporter Antibody

serum, Chemicon®

Synonyme(s) :

Serotonin transporter antibody

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

rabbit

Niveau de qualité

Forme d'anticorps

serum

Type de produit anticorps

primary antibodies

Clone

polyclonal

Espèces réactives

mouse, rat

Fabricant/nom de marque

Chemicon®

Technique(s)

immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

Spécificité

Serotonin Transporter. By Western blot the antibody recognizes a strong band at ~64 kDa in rat brain extract. The antibody is suitable for detection of the serotonin transporter in the CNS, PNS and peripheral organs where the transporter is present.

Immunogène

Fusion protein from the N-terminal of rat Serotonin Transporter.

Application

Anti-Serotonin Transporter Antibody is an antibody against Serotonin Transporter for use in IH, IP & WB.
Immunohistochemistry on 4% paraformaldehyde fixed tissues.
Research Category
Neuroscience
Research Sub Category
Ion Channels & Transporters

Forme physique

Liquid

Stockage et stabilité

Maintain at -20°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.

Informations légales

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Nidhi Kaushal et al.
Neuropharmacology, 61(5-6), 992-1000 (2011-07-19)
Methamphetamine (METH) is a highly addictive psychostimulant drug of abuse. Low and high dose administration of METH leads to locomotor stimulation, and dopaminergic and serotonergic neurotoxicity, respectively. The behavioral stimulant and neurotoxic effects of METH can contribute to addiction and
Michael J Seminerio et al.
Pharmacology, biochemistry, and behavior, 98(1), 12-20 (2010-12-07)
Methamphetamine interacts with sigma (σ) receptors and AC927, a selective σ receptor ligand, protects against methamphetamine-induced dopaminergic neurotoxicity. In the present study, the effects of AC927 on methamphetamine-induced hyperthermia and striatal serotonergic neurotoxicity were evaluated. Male, Swiss Webster mice were
Alessandro Luchetti et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(25), 4936-4944 (2020-05-18)
Hippocampus receives dense serotonergic input specifically from raphe nuclei. However, what information is carried by this input and its impact on behavior has not been fully elucidated. Here we used in vivo two-photon imaging of activity of hippocampal median raphe
Xiufang Cui et al.
Molecular medicine reports, 21(4), 1934-1940 (2020-04-23)
Serotonin‑selective reuptake transporter (SERT) regulates extracellular availability of serotonin (5‑hydroxytryptamine; 5‑HT) and participates in the pathogenesis of functional disorders. Colonic SERT expression is decreased in colonic sensitized rats, and the glucagon‑like peptide‑1 analogue, exendin‑4, reduces visceral hypersensitivity by decreasing 5‑HT
Samuel J Erb et al.
The Journal of biological chemistry, 291(38), 19725-19733 (2016-07-20)
Depression is a significant public health problem for which currently available medications, if effective, require weeks to months of treatment before patients respond. Previous studies have shown that the G protein responsible for increasing cAMP (Gαs) is increasingly localized to

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