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TACR3 belongs to a family of genes that function as receptors for tachykinins. Additionally we are shipping Tachykinin Receptor 3 Kits (32) and Tachykinin Receptor 3 Proteins (4) and many more products for this protein.
Showing 10 out of 90 products:
Human Polyclonal TACR3 Primary Antibody for EIA, IHC (p) - ABIN500361
Ding, Lü, Guan, Wang, Xu, Li et al.: Neurokinin B receptor (NK3)-containing neurons in the paraventricular and supraoptic nuclei of the rat hypothalamus synthesize vasopressin and express Fos following intravenous injection of ... in Neuroscience 1999
Show all 4 references for ABIN500361
Human Polyclonal TACR3 Primary Antibody for IHC (p), WB - ABIN318919
Haley, Flynn: Tachykinin NK3 receptor contribution to systemic release of vasopressin and oxytocin in response to osmotic and hypotensive challenge. in American journal of physiology. Regulatory, integrative and comparative physiology 2007
Show all 2 references for ABIN318919
Human Polyclonal TACR3 Primary Antibody for WB - ABIN658143
Kalsi, Kuo, Aliev, Alexander, McMichael, Patterson, Walsh, Zhao, Schuckit, Nurnberger, Edenberg, Kramer, Hesselbrock, Tischfield, Vladimirov, Prescott, Dick, Kendler, Riley: A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts. in Human molecular genetics 2010
mutations in TAC (show IL2RA Antibodies) and TACR3 are not a common cause for ICPP.
None of the 4 single polymorphisms studied in TACR3 are linked directly to puberty onset time, but A63P in TAC3 (show TAC3 Antibodies) is statistically associated with precocious puberty.
Elevated CRP (show CRP Antibodies) is likely a pathogenic factor contributing to preeclampsia by binding to phosphocholinated neurokinin B and preferentially activating NK3R.
data indicate that GPR54 (show KISS1R Antibodies) and TACR3 gene mutations are not a frequent cause of ICPP. The identified A/G synonymous SNP (dbSNP ID: rs10407968) located in exon 1 of the gene is not likely to have a pathogenic role in exon splicing
Studies indicate the molecular mechanisms by which NK3R mutations cause GnRH deficiency.
Expression of the gene encoding TACR3 is significantly up-regulated in leiomyomas, compared with matched myometrium.
Rare variants in the TAC3 (show TAC3 Antibodies) and TACR3 genes were identified in patients with central pubertal disorders and loss-of-function variants of TACR3 were associated with the normosmic IHH (show IHH Antibodies) phenotype.
Data suggest that mutations in TACR3 and GNRHR (show GNRHR Antibodies) are the most common causative mutations in normosmic idiopathic hypogonadotropic hypogonadism in families in Turkey.
NKB (show TAC3 Antibodies)/NK(3)R and kisspeptin/KISS1R (show KISS1R Antibodies) are present in female peripheral reproductive tissues with colocalization of both systems in some non-neuronal cell populations of the human female genital tract.
The gonadotropin axis dysfunction associated with nCHH due to TAC3 (show TAC3 Antibodies)/TACR3 mutations is related to a low GnRH (show GNRH1 Antibodies) pulsatile frequency leading to a low frequency of alpha-subunit (show POLG Antibodies) pulses and to an elevated FSH (show BRD2 Antibodies)/LH ratio.
Data suggest that activation of neurokinin 3 and kappa-opioid receptors (NK3R and KOR (show OPRK1 Antibodies)) excites and inhibits kisspeptin, neurokinin B (NKB), and dynorphin (KNDy neurons).
NKB (show TAC3 Antibodies)-NK3R signaling plays a role in pubertal maturation; its alterations may contribute to pubertal disorders linked to metabolic stress and negative energy balance.
although capable of fertility, Tacr3-deficient mice have central reproductive defects
neurokinin 3 receptor activation in the median preoptic nucleus modulates body temperature
Tachykinin NK3 receptor genes are expressed in uterine cells, oocytes, ovaries and embryos from mice, and may play a role in female reproductive function.
The co-expression of NK-3R and NMDA/AMPA (show GRIA3 Antibodies) receptor subunits in the nigral neurons has provided a structural basis for functional modulation of neuronal glutamate (show GRIN1 Antibodies) receptors by neurokinin-3.
In neurokinin 1 receptor knockout retinas no major changes were detected: neurokinin 3 receptor mRNA levels as well as substance P (show TAC1 Antibodies) and neurokinin 3 receptor immunostainings were similar to wild types.
these results support a role for the NK(3) receptor in performance of operant tasks and in spatial learning but not in working memory
Together, these results support a role for the NK3 receptor in reactivity to dopaminergic stimuli, but the lack of robust changes indicates that the sensitivity to dopamine may be activity-dependent or benign in nature.
Evidence for tachykinin NK3 receptors-triggered peptide YY release from isolated guinea-pig distal colon
[MePhe]-NKB and senktide caused bronchoconstriction in guinea pig through activation of the tachykinin NK-receptors but the tachykinin NK- and/or NK-receptors are also involved in the response.
This gene belongs to a family of genes that function as receptors for tachykinins. Receptor affinities are specified by variations in the 5'-end of the sequence. The receptors belonging to this family are characterized by interactions with G proteins and 7 hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin neurokinin 3, also referred to as neurokinin B.
tachykinin receptor 3
, neuromedin-K receptor-like
, NK-3 receptor
, neurokinin B receptor
, neurokinin beta receptor
, neuromedin-K receptor
, Nk3 receptor
, neurokinin 3 receptor
, neuromedin K receptor
, Neuromedin K receptor (Neurokinin B/Tachikin 3)
, tachikin receptor 3
, neurokinin receptor subtype NK3
, neurokinin-3 receptor
, tachykinin neurokinin-3 receptor