磷酸化神经色氨酸羟化酶2抗体
规格：1mg/1ml
英文名： phospho-TPH2 (Ser19)
别名： TPH2 (phospho S19); p-TPH2 (phospho S19); MGC138871; ADHD7; FLJ37295; HGNC:20692; MGC138872; Neuronal tryptophan hydroxylase; NTPH; TPH 2; Tph2; TPH2_HUMAN; TRPO; Tryptophan 5-hydroxylase 2; Tryptopha
分子量： 56kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：Polyclonal
亚型：IgG
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthesised phosphopeptide derived from human
交叉反应：Human, Dog, Horse,
细胞定位：
磷酸化神经色氨酸羟化酶2抗体产品介绍：background: Phenylalanine hydroxylase (PAH), tyrosine hydroxylase (TH), tryptophan hydroxylase (TPH) and tryptophan hydroxylase 2 (TPH2) comprise a small family of monooxygenases that catalyze the rate-limiting step in the catabolism of aromatic L-amino acids and utilize tetrahydropterine as a cofactor. TPH2 is highly expressed in the central nervous system (CNS), mainly in the brain. TPH2 catalyzes the first step in the biosynthesis of serotonin in the CNS and melatonin in the pineal gland, and may be involved in the pathology of several neuropsychiatric disorders. Glucocorticoid-mediated reduction of TPH2 is associated with the etiology of mood disorders, specifically psychotic major depression, and TPH2 may be related to dysregulation of serotonin neurotransmission in the brain which commonly leads to suicidal behavior. Tissue Specificity: Brain specific. DISEASE: Genetic variation in TPH2 may influence susceptibility to major 磷酸化神经色氨酸羟化酶2抗体depressive disorder (MDD) [MIM:608516]. Defects in TPH2 are the cause of susceptibility to attention deficit-hyperactivity disorder type 7 (ADHD7) [MIM:613003]. ADHD is a neurobehavioral developmental disorder and is primarily characterized by the co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone. Note=Naturally occurring variants of TPH2 with impaired 磷酸化神经色氨酸羟化酶2抗体enzyme activity could cause deficiency of serotonin production and result in an increased risk of developing behavioral disorders. Similarity: Belongs to the biopterin-dependent aromatic amino acid hydroxylase family. Contains 1 ACT domain. Database links: Entrez Gene: 618062 Cow Entrez Gene: 216343 Mouse Entrez Gene: 317675 Rat Entrez Gene: 407712 Zebrafish Entrez Gene: 415103 Zebrafish SwissProt: Q2KIQ5 Cow SwissProt: Q8CGV2 Mouse SwissProt: Q8CGU9 Rat Unigene: 31597 Mouse Unigene: 28510 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
磷酸化神经色氨酸羟化酶2抗体产品应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：细胞生物 神经生物学 信号转导 糖尿病
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid