Product overview

Name TAT-D1 Peptide
Purity >95%
Description Selective D1-D2 heteromer antagonist
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Biological Data

Biological description Selective Dopamine D1-D2 heteromer antagonist which occludes the interaction site between the two receptors to inhibit D1-D2 heteromer expression and function. Alleviates behavioural despair symptoms and exerts antidepressant-like effects. Active in vivo.

Solubility & Handling

Storage instructions -20°C
Solubility overview Soluble in PBS (1 mg/ml), and in DMSO
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

Molarity

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Dilution

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Chemical Data

Purity >95%
Molecular Weight 3472.97
Molecular Formula C144H257N57O43

References for TAT-D1 Peptide

References are publications that support the biological activity of the product
  • Mitochondria-derived peptide SHLP2 regulates energy homeostasis through the activation of hypothalamic neurons.

    Kim SK et al (2023) Nature communications 14 : 4321
  • Effects of Mitochondrial-Derived Peptides (MDPs) on Mitochondrial and Cellular Health in AMD.

    Nashine S et al (2020) Cells 9 :
  • Modulation and functions of dopamine receptor heteromers in drugs of abuse-induced adaptations.

    Andrianarivelo A et al (2019) Neuropharmacology 152 : 42-50
  • The dopamine D1-D2 receptor heteromer exerts a tonic inhibitory effect on the expression of amphetamine-induced locomotor sensitization.

    Shen MY et al (2015) Pharmacology, biochemistry, and behavior 128 : 33-40
  • A peptide targeting an interaction interface disrupts the dopamine D1-D2 receptor heteromer to block signaling and function in vitro and in vivo: effective selective antagonism.

    Hasbi A et al (2014) FASEB journal : official publication of the Federation of American Societies for Experimental Biology 28 : 4806-20

5 Item(s)