TPH2 Antibody

中文名稱：

TPH2兔多克隆抗體
貨號：

CSB-PA809000LA01HU
規格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human liver tissue using CSB-PA809000LA01HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human colon cancer using CSB-PA809000LA01HU at dilution of 1:100

Immunofluorescent analysis of HepG2 cells using CSB-PA809000LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)

Western Blot
Positive WB detected in: Rat heart tissue, Mouse stomach tissue
All lanes: TPH2 antibody at 3μg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 57 kDa
Observed band size: 57 kDa
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) TPH2 Polyclonal antibody
Uniprot No.：

Q8IWU9
基因名：

TPH2
別名：

TPH2; NTPH; Tryptophan 5-hydroxylase 2; Neuronal tryptophan hydroxylase; Tryptophan 5-monooxygenase 2
宿主：

Rabbit
反應種屬：

Human, Mouse, Rat
免疫原：

Recombinant Human Tryptophan 5-hydroxylase 2 protein (44-225AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，TPH2 Antibody (CSB-PA809000LA01HU)，的標記方式是Non-conjugated。對于TPH2 Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產品名稱	應用
HRP	CSB-PA809000LB01HU	TPH2 Antibody, HRP conjugated	ELISA
FITC	CSB-PA809000LC01HU	TPH2 Antibody, FITC conjugated
Biotin	CSB-PA809000LD01HU	TPH2 Antibody, Biotin conjugated	ELISA

克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA, WB, IHC, IF

推薦稀釋比：

Application	Recommended Dilution
WB	1:200-1:5000
IHC	1:20-1:200
IF	1:50-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) Protocol
Immunofluorescence (IF) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

基因功能參考文獻：
1. These findings indicate that TPH1, TPH2, and SLC6A4 variants moderate the subjective effects of cocaine in non-treatment-seeking cocaine-dependent participants. PMID: 28590957
2. results provide new evidence for the role of regulatory genetic variants that could modulate human TPH2 expression in the antidepressant response to fluoxetine. PMID: 28456685
3. This study firstly demonstrated evidence for an association between aberrant cortical folding in the PFC and ACC and TPH2 polymorphism gene related to the pathophysiology of major depressive disorder. PMID: 27807918
4. This study shown that theTPH2 genotype is likely to modulate the risk for addictive behaviors in PD on dopaminergic therapy. PMID: 27237108
5. social anxiety disorder entails an overactive presynaptic serotonergic system that, in turn, seems functionally influenced by the TPH2 G-703T polymorphism in emotionally relevant brain regions PMID: 27189957
6. nine ADHD candidate single nucleotide polymorphisms (SNPs) in seven genes were tested for association with PD in 5333 cases and 12,019 healthy controls. No significant association was observed. PMID: 28176268
7. Tryptophan hydroxylase synthesizes Serotonin and is over-expressed in Suicides.TPH2 mRNA was greater in Suicide Nonsmokers than Suicide Smokers.The absence of altered TPH2 expression in non-suicide smokers suggests no pharmacological effect of Smoking. PMID: 26954509
8. This study shown the significant results were found with TPH2 rs4570625 involved with fast visual processing as assessed by metacontrast. PMID: 27926628
9. Genetic variation in TPH2 is associated with antidepressant response and may also interact with childhood trauma to influence outcome of antidepressant treatment. PMID: 27521242
10. 2-way interaction between TPH2 rs4290270 and general traumas revealed that TT homozygotes with history of general traumas had an increased risk for suicide attempt. 3-way interaction of general traumas, TPH2 rs4290270 and ADARB1 rs4819035 indicated that highest predisposition to suicide attempt was observed in individuals who experienced general traumas and were TT homozygote for rs4290270 and TT homozygote for rs4819035. PMID: 28084537
11. The catalytic domain of TPH1 shares a sequence identity of 81% with TPH2. Despite the high sequence identity, differences in the kinetic parameters of the isoforms have been identified; i.e., only TPH1 displays substrate tryptophan inhibition. PMID: 29035515
12. results confirm the role of TPH1, TPH2, 5HT2A, CRHR1 and ACP1 variants in the risk of suicidal behavior. PMID: 27479537
13. There was no association between rs11179000, rs136494 and rs4570625 polymorphisms of the tryptophan hydroxylase 2 gene and major depressive disorder in a sample of the Colombian population PMID: 28193370
14. This study demonstrates that both TPH1 and TPH2 are expressed in human and mouse placenta throughout pregnancy and helps to better understand the placental serotonin system, which is crucial for healthy pregnancy and fetal development. PMID: 28751217
15. This study provides the first evidence that, at least among Han Chinese patients with PD, AC genotype at rs78162420 in the TPH2 gene increase risk of depression. PMID: 28320136
16. interaction between SNP rs4570625 and BDNF Val66Met predicts a high-Risk emotional phenotype PMID: 27695066
17. Subjects with the TPH2 rs4570625 TT genotype, especially males, exhibit less aggression and a favourable impulsivity profile, and develop anxiety disorders by young adulthood less often PMID: 28342337
18. Study reports an association between functional variation on the TPH2 promotor region and rich club-a densely mutually connected set of hub regions in the brain, thought to serve as a processing and integration core-organization PMID: 26975194
19. Altered TPH2 expression in colonic serotonergic nerves of patients with Hirschsprung's disease complicated by enterocolitis may contribute to intestinal secretory and motor disturbances, including recurrent HAEC. PMID: 27217698
20. The purposes of this study were to investigate the potential association of TPH-2 polymorphisms with susceptibility to ODD in a Han Chinese school population. In single marker analyses,there was a significant difference in the genotype (chi (2) = 4.163, P = 0.041) and allele frequency (chi (2) = 3.930, P = 0.047) of rs1386494 between ODD and control groups. PMID: 27871272
21. the association studies between TPH2 and Bipolar disorder was investigated. PMID: 26365518
22. Carriers of the TPH-2 allele may be at increased risk for PTSD. COMT rs4633C and TPH-2 rs11178997T alleles jointly explained 7% of the variance in PTSD severity scores. These findings provide biological support for dividing DSM-IV category C symptoms into DSM-5 categories C and D. PMID: 25451452
23. Study demonstrated that 5-HTTLPR, VNTR In2, and TPH2 rs1386497 polymorphisms mediate working memory performance and that their effects on working memory depend on cocaine use of participants PMID: 26013962
24. We also found that early family structure directly influences the levels of dysregulation problems in early adolescence, both alone and in interaction with TPH2. PMID: 26583347
25. Chinese Han individuals with at least oners11178997T allele or rs120074175A allele are susceptible to MD even in the relative absence of high-negative life events. PMID: 26386440
26. loss of function mutation in Tph2 results in greater motivation for ethanol consumption under aversive conditions and may confer enhanced sensitivity to alcohol use disorder PMID: 26497913
27. TPH2 expression is regulated by DNA methylation of the TPH2 promoter region in patients with major depressive disorder. PMID: 25955598
28. results provide evidence for an association between the rs7305115 polymorphism of the TPH-2 gene and suicidal behavior in a Mexican population. PMID: 26028568
29. mood disorders and HTR1A G allele variation, the C-1019G polymorphism of the transcriptional control region of the 5-HT1A receptor, independently predicted the incidence of IFN-induced depression in HCV patients PMID: 26001668
30. A potential role of TPH2 in alcohol dependencies suggested. TPH2 genetic variability may be also associated with anxiety and aggression traits in alcohol dependent subjects. PMID: 26232682
31. 1,25-Dihydroxyvitamin D regulates expression of the tryptophan hydroxylase 2 and leptin genes: implication for behavioral influences of vitamin D. PMID: 26071405
32. Case-control genetic association study in multi-ethnic Malaysian population. Strong linkage disequilibrium was detected between rs1386495 and rs1386494 in pooled subjects; however, no significant association was found in the haplotype analysis. PMID: 24376086
33. TPH2 polymorphism may be associated with cognitive function in late onset depression patients. PMID: 26057341
34. With regard to G-703 T/A-473 T/G19918A TPH-2 variants, this up-to-date meta-analysis could not detect any significant association between those genetic variants and suicidal behavior .[review and meta-analysis] PMID: 25005534
35. genetic contribution to phenotypic facets related to obsessive-compulsive symptoms and perfectionism in healthy subjects; association of TPH2 s4570625 and DRD2 TaqIA SNPs with the subscales scrupulousness and perseverance of the BFQ factor conscientiousness were found PMID: 25283578
36. results provide evidence on the possible role of genetic variations in 5-HT neurotransmission on development of personality traits, and suggest a functional interaction between two key proteins in the serotonergic system. PMID: 25455586
37. The results of this study indicated that in the Han Chinese population TPH2 may be a potential susceptibility gene for bipolar disorder. Further studies are needed to validate this association. PMID: 25152196
38. findings support that TPH2 may play an important functional role in the development of PTSD and contribute to the limited literature regarding the genetic basis and the sex-specific expression of PTSD's symptoms PMID: 25014617
39. This study showed that an interaction among childhood abuse and genetic variants of TPH2. PMID: 25214390
40. Data show that a marginal association between TPH2 rs11179023 and symptom improvement was observed in only the group of major depressive disorder patients treated with interpersonal counseling. PMID: 24958631
41. Tryptophan hydroxylase 2 gene allele variants might be risk factors for psychiatric conditions in TLE [temporal lobe epilepsy ]. PMID: 24491795
42. findings suggest that greater TPH2 gene expression is the basis for more TPH2 protein in the Dorsal Raphe Nucleus and Median Raphe Nucleus in alcoholics. PMID: 24942188
43. TPH2 variant and maternal stress and depression are associated with difficulty disengaging attention from fearful facial expressions. PMID: 24304270
44. Results show that a single nucleotide loss of function polymorphism in tph2 is sufficient to induce gene-dose-dependent cognitive deficits in mice PMID: 24196946
45. The main finding was that carriers homozygous for the G allele(TPH2 -703 G/T) showed increased target-related induced gamma-band synchronization when combined with the A/A genotype of the (NE) transporter variation. PMID: 23258345
46. Our findings suggest that common genetic variations of TPH2 are likely to contribute to genetic susceptibility to paranoid schizophrenia in Han Chinese. PMID: 24668623
47. polymorphic tph2 enzyme has increased activity, but decreased enzyme stability and serotonin production PMID: 24899127
48. None of the genetic markers within SLC6A4, MAOA, TPH1 and TPH2 were significantly associated with completed suicide or suicide method in the basic association tests. PMID: 23313272
49. The results of this study showed no association between tryptophan TPH2 gene polymorphisms and the complication of medication overuse headaches in patients with migraines. PMID: 24458851
50. None of the three gene variants, 5-HTTLPR, COMTval158met and TPH2 G-703T, was associated with long-term response to CBT for SAD. PMID: 24260145
顯示更多

收起更多
相關疾病：

Major depressive disorder (MDD); Attention deficit-hyperactivity disorder 7 (ADHD7)
蛋白家族：

Biopterin-dependent aromatic amino acid hydroxylase family
組織特異性：

Brain specific.
數據庫鏈接：

HGNC: 20692

OMIM: 607478

KEGG: hsa:121278

STRING: 9606.ENSP00000329093

UniGene: Hs.736576

Most popular with customers

YWHAG Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
XRCC5 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC, IF

Species Reactivity: Human
XPNPEP1 Recombinant Monoclonal Antibody

Applications: ELISA, IHC, FC

Species Reactivity: Human
XDH Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WT1 Recombinant Monoclonal Antibody

Applications: ELISA, WB, IHC

Species Reactivity: Human
WFDC2 Recombinant Monoclonal Antibody

Applications: ELISA, WB, FC

Species Reactivity: Human
VIM Recombinant Monoclonal Antibody

Applications: ELISA, IHC, IF

Species Reactivity: Human