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  • mProX™ Human TAAR1 Stable Cell Line

    [CAT#: S01YF-0923-KX63]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Based on this stable cell line, we also provide cell-based in vitro assays to evaluate the effects of your compounds or antibodies.

    Sub Cat Product Name Target Protein Species Host Cell Type Assay Types Inquiry Datasheet
    S01YF-1122-KX969 Magic™ Rhesus macaque TAAR1 in Vitro cAMP Assay Rhesus monkey CHO-K1 cAMP Assay

    Product Information

    Target Protein
    TAAR1
    Target Family
    Trace Amine Family
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1; HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Cancer Research; CNS Research
    Related Diseases
    Superficial Urinary Bladder Cancer; Hypoparathyroidism-Deafness-Renal Disease Syndrome
    Gene ID
    UniProt ID

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The six functional human trace amine-associated receptors, or TAARs, are so termed because they can bind endogenous amines, which are found in trace amounts in tissues. TAAR1 is one of these receptors. Dopamine, norepinephrine, and serotonin neurons in the CNS are regulated by TAAR1 in a major way. Additionally, it has an impact on the immunological and monoaminergic systems via several methods. The immune system's TAAR1 uses active PKA and PKC phosphorylation cascades to relay information. Methamphetamine was found to have these effects in some studies, indicating that in addition to regulating brain monoamine levels, amphetamine-related substances may also have an impact on the immune system. One of the downstream consequences of activated TAAR1 in monoaminergic systems is to elevate cAMP in the presynaptic cell by activating adenylyl cyclase via Gαs. The customized TAAR1 stable cell line can be used in antibody discovery and development, potential drug candidate screening and signaling pathway researches.

    Protocols

    Please visit our protocols page.

    Customer Reviews

    chat Maria

    I was very pleased with the QCs of the cell line. Jun 16 2023

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    chat Dwight

    I had a wonderful encounter with this business. Excellent client service was provided. Aug 19 2022

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    FAQ

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    Published Data

    Fig.1 Following intrastriatal or MFB 6-OHDA injection, the levels of TH and the dopamine transporter were compared in WT and TAAR1 KO mice.

    Injections of striatal 6-OHDA decreased the levels of TH in the striatal tissue of mice with WT and TAAR1 KO mutations. In comparison to WT mice, TH levels were greater in the intact and lesioned hemispheres of TAAR1 KO mice.

    Ref: Alvarsson, Alexandra, et al. "Modulation by trace amine-associated receptor 1 of experimental parkinsonism, L-DOPA responsivity, and glutamatergic neurotransmission." Journal of Neuroscience 35.41 (2015): 14057-14069.

    Pubmed: 26468205

    DOI: 10.1523/JNEUROSCI.1312-15.2015

    Research Highlights

    The mammalian brain exhibits widespread expression of TAAR1, particularly in limbic and monoaminergic regions thought to be involved in mood, attention, memory, fear, and addiction. Since the TAAR1 signal is primarily intracellular, it is currently unclear how TAAR1 is distributed inside cells.
    Rutigliano, Grazia, Alice Accorroni, and Riccardo Zucchi. "The case for TAAR1 as a modulator of central nervous system function." Frontiers in pharmacology 8 (2018): 987.
    Pubmed: 29375386   DOI: 10.3389/fphar.2017.00987

    The ability of the trace amine-associated receptor 1 (TAAR1) to influence monoaminergic and glutamatergic neurotransmission has made it an attractive therapeutic target for neuropsychiatric illnesses. Due to the TAAR1-mediated control of dopaminergic tone, agonist drugs have attracted attention as potential therapies for schizophrenia and other psychoses.
    Dedic, Nina, et al. "Therapeutic potential of TAAR1 agonists in schizophrenia: evidence from preclinical models and clinical studies." International Journal of Molecular Sciences 22.24 (2021): 13185.
    Pubmed: 34947997   DOI: 10.3390/ijms222413185

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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