phospho-TPH2 (Ser19) Rabbit pAb (一抗) | Bioss

2026-03-02~2026-04-30,KXJ26032026-03-02~2026-04-30,促销赠品
phospho-TPH2 (Ser19) Rabbit pAb (一抗) | Bioss
货号:bs-17166R
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概述

产品编号
bs-17166R
产品类型
磷酸化抗体、宠物抗体、农牧业/家禽抗体
英文名称
phospho-TPH2 (Ser19) Rabbit pAb
中文名称
磷酸化神经色氨酸羟化酶2抗体
英文别名
TPH2 (phospho-S19); p-TPH2; phospho-TPH2; TPH2 (phospho-Ser19); ADHD7; NTPH; T23O_BOVIN; TDO2; TDO; Tryptamin 2,3-dioxygenase; Tryptophan oxygenase (TO | TRPO); Tryptophan pyrrolase; Tryptophanase; 1.13.11.11; TPH2_HUMAN; TPH2; Neuronal tryptophan hydroxylase; Tryptophan 5-monooxygenase 2; 1.14.16.4; TPH2_MOUSE; TPH2_RAT;
抗体来源
Rabbit
免疫原
KLH conjugated synthesised phosphopeptide derived from human TPH2 around the phosphorylation site of Ser19: GF(p-S)LD
亚型
IgG
性状
Liquid
纯化方法
affinity purified by Protein A
克隆类型
Polyclonal
理论分子量
56 kDa
浓度
1mg/ml
储存液
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SWISS
Gene ID
保存条件
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
背景资料
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.
磷酸化神经色氨酸羟化酶2抗体-bs-17166R

产品应用

应用已检合格种属预测种属推荐稀释比例
IHC-PRatHuman, Dog, Horse1:100-500
IHC-FRatHuman, Dog, Horse1:100-500
IFRatHuman, Dog, Horse1:100-500

交叉反应

交叉反应: Rat (predicted: Human, Dog, Horse)

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靶标

基因名
TPH2
蛋白名
Tryptophan 5-hydroxylase 2
组织特异性
Brain specific.
疾病
Genetic variation in TPH2 may influence susceptibility to major 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 enzyme activity could cause deficiency of serotonin production and result in an increased risk of developing behavioral disorders.
相似性
Belongs to the biopterin-dependent aromatic amino acid hydroxylase family.
Contains 1 ACT domain.

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