PER3 Antibody, FITC conjugated

說明書

中文名稱：

PER3兔多克隆抗體, FITC偶聯
貨號：

CSB-PA017788LC01HU
規格：

￥880
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) PER3 Polyclonal antibody
Uniprot No.：

P56645
基因名：

PER3
別名：

2810049O06Rik antibody; Cell growth inhibiting gene 13 protein antibody; Cell growth-inhibiting gene 13 protein antibody; Circadian clock protein PERIOD 3 antibody; GIG13 antibody; gPER3 antibody; Growth inhibiting protein 13 antibody; HGNC:8847 antibody; hPER3 antibody; mPer3 antibody; Per3 antibody; PER3_HUMAN antibody; Period 3 antibody; Period circadian clock 3 antibody; Period circadian protein 3 antibody; Period circadian protein homolog 3 antibody; Period homolog 3 (Drosophila) antibody; Period homolog 3 antibody; Period homolog 3; Drosophila antibody; Period3 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Period circadian protein homolog 3 protein (1-131AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

FITC
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
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

功能：

Originally described as a core component of the circadian clock. The circadian clock, an internal time-keeping system, regulates various physiological processes through the generation of approximately 24 hour circadian rhythms in gene expression, which are translated into rhythms in metabolism and behavior. It is derived from the Latin roots 'circa' (about) and 'diem' (day) and acts as an important regulator of a wide array of physiological functions including metabolism, sleep, body temperature, blood pressure, endocrine, immune, cardiovascular, and renal function. Consists of two major components: the central clock, residing in the suprachiasmatic nucleus (SCN) of the brain, and the peripheral clocks that are present in nearly every tissue and organ system. Both the central and peripheral clocks can be reset by environmental cues, also known as Zeitgebers (German for 'timegivers'). The predominant Zeitgeber for the central clock is light, which is sensed by retina and signals directly to the SCN. The central clock entrains the peripheral clocks through neuronal and hormonal signals, body temperature and feeding-related cues, aligning all clocks with the external light/dark cycle. Circadian rhythms allow an organism to achieve temporal homeostasis with its environment at the molecular level by regulating gene expression to create a peak of protein expression once every 24 hours to control when a particular physiological process is most active with respect to the solar day. Transcription and translation of core clock components (CLOCK, NPAS2, ARNTL/BMAL1, ARNTL2/BMAL2, PER1, PER2, PER3, CRY1 and CRY2) plays a critical role in rhythm generation, whereas delays imposed by post-translational modifications (PTMs) are important for determining the period (tau) of the rhythms (tau refers to the period of a rhythm and is the length, in time, of one complete cycle). A diurnal rhythm is synchronized with the day/night cycle, while the ultradian and infradian rhythms have a period shorter and longer than 24 hours, respectively. Disruptions in the circadian rhythms contribute to the pathology of cardiovascular diseases, cancer, metabolic syndromes and aging. A transcription/translation feedback loop (TTFL) forms the core of the molecular circadian clock mechanism. Transcription factors, CLOCK or NPAS2 and ARNTL/BMAL1 or ARNTL2/BMAL2, form the positive limb of the feedback loop, act in the form of a heterodimer and activate the transcription of core clock genes and clock-controlled genes (involved in key metabolic processes), harboring E-box elements (5'-CACGTG-3') within their promoters. The core clock genes: PER1/2/3 and CRY1/2 which are transcriptional repressors form the negative limb of the feedback loop and interact with the CLOCK|NPAS2-ARNTL/BMAL1|ARNTL2/BMAL2 heterodimer inhibiting its activity and thereby negatively regulating their own expression. This heterodimer also activates nuclear receptors NR1D1, NR1D2, RORA, RORB and RORG, which form a second feedback loop and which activate and repress ARNTL/BMAL1 transcription, respectively. Has a redundant role with the other PER proteins PER1 and PER2 and is not essential for the circadian rhythms maintenance. In contrast, plays an important role in sleep-wake timing and sleep homeostasis probably through the transcriptional regulation of sleep homeostasis-related genes, without influencing circadian parameters. Can bind heme.
基因功能參考文獻：
1. Study identified several CpG sites and specifically several CpGs in the PTPRS and PER3 genes differentially methylated between obese and non-obese children, suggesting a role for DNA methylation concerning development of childhood obesity. PMID: 28614626
2. these findings suggest that rhythmic expression of the circadian clock gene PER3 is associated with the amount of daily physical activity and physical fitness in older adults PMID: 28045078
3. PER3 polymorphisms links with chronotype and affective dimensions PMID: 28708003
4. data suggest that, PER3(4/4) genotype may accelerate the course of disease in multiple sclerosis susceptible individuals especially in women PMID: 29055480
5. The impact of PER3 polymorphisms on sleep cycle and insomnia in older adults is reported. PMID: 28276850
6. there is a significant association between the PER3 polymorphism and the extraversion personality trait PMID: 28055273
7. PER34/4 genotype may accelerate the course of disease in multiple sclerosis susceptible individuals. PMID: 29055479
8. CLOCK rs1801260*C and PER3(4/4) influence myelination processes by regulating sleep quality and quantity. PMID: 27996307
9. 4 and 5 variable-number tandem-repeat polymorphisms appear to influence sensitivity to the effects of stressful urban environments on sleep PMID: 27593530
10. Data suggest that three E box-like response elements are located upstream of PER3 transcription start sites; these response elements appear to additively contribute to cell-autonomous transcriptional oscillation of PER3 and other circadian proteins. PMID: 28821614
11. This study showed that Lack of Association between Genetic Polymorphism of PER3 gene with Late Onset Depression and Alzheimer's Disease in a Sample of a Brazilian Population PMID: 27335043
12. This study shown a possible association between Per3 polymorphism and consciousness recovery level in Disorders of Consciousness patients. PMID: 26359345
13. PER3 variants may be associated with decreased risk for depressive symptoms, including subthreshold levels of depressive symptoms, in older adults. PMID: 25892098
14. The PER1 c.2884C > G polymorphism and PER3 54bp VNTR were associated with annual percent changes in bone mineral density of femoral neck after 1 year of hormone therapy. PMID: 26624862
15. PER3 polymorphism is associated with sleep quality after a mild traumatic brain injury. PMID: 26440425
16. PER3 VNTR polymorphism influences both response to antidepressant chronotherapeutics and total sleep time after the repeated sleep deprivation treatment in patients with bipolar depression. PMID: 26707349
17. No association between cluster headache, PER3 VNTR polymorphism and chronotype was found in this study. PMID: 26922944
18. There was no significant association between the PER3 VNTR polymorphism and the irregularity of the menstrual cycle in Korean adolescents. PMID: 26453284
19. A role for PER3 in modulating circadian clock and mood during seasonal changes PMID: 26903630
20. This work suggests a role of PER3 rs10462020 in predicting a prognosis in Diffuse large B-cell lymphoma overall survival of patients. PMID: 26406960
21. evidence of an association between PER3 gene and planning performance in a sample of healthy subjects PMID: 25798540
22. PER3 VNTR genotype does not explain the difference in chronotype between South African and Dutch marathon runners PMID: 26102236
23. minor polymorphisms of PER3 may be associated with poor morning gastric motility, and may have a combinatorial effect with CLOCK. PMID: 25775462
24. The findings support the notion that PER3 polymorphisms could be a potential genetic marker for an individual's circadian and sleep phenotypes. PMID: 25201053
25. PER3 long allele carriers were more vulnerable to sleep-loss associated attentional lapses than those with the short allele. PMID: 25940842
26. length polymorphism in the Period 3 gene is associated with sleepiness and maladaptive circadian phase in night-shift workers PMID: 25545397
27. In patients with non-small cell lung cancer, those with lower expression of Per1, Per2 and Per3 had a shorter survival time than those with higher expression. PMID: 25550826
28. PERIOD3 clock gene length polymorphism may have a role in colorectal adenoma formation PMID: 25501848
29. The data indicate that humans homozygous for the PER3(5/5) allele are more sensitive to NIF light effects, as indexed by specific changes in sleep EEG activity. PMID: 24893318
30. no evidence supporting a global association of PER3 genetic variants with the incidence of cancer (Meta-Analysis) PMID: 25837749
31. The polymorphisms studied in PER3 did not demonstrate any relationship with Bone Mineral Density or the odds of osteoporosis in postmenopausal Korean women. PMID: 24678593
32. Provide some evidence that circadian rhythm of flight cadets with the PER3 (5) allele are less likely to be affected compared to those with the PER3 (4) allele. PMID: 25400784
33. A wild genotype of rs228729 in PER3 was the primary risk factor contributing to Chinese hepatocellular carcinoma patients recurrence-free survival. PMID: 25344870
34. An association is outlined of Per3 five repeat allele with T2DM occurrence and suggest that individuals with five repeat allele may be at a greater risk for T2DM as compared to those carrying the four repeat allele. PMID: 25390010
35. PER3, at least partially, was targeted by miRNA-103, which might affect cells apoptosis in G2/M phase by modulating apoptosis-related gene in p53 pathway. PMID: 24393525
36. Per3 VNTR may contribute to modulation of cardiac functions and interindividual differences in development and progression of myocardial infarction PMID: 24866331
37. Per3 variable number tandem repeat polymorphism is not a major risk factor for chronic heart failure (CHF) or a factor modulating the severity of the CHF in this population. PMID: 23128810
38. there is significant association between diurnal preference and a polymorphism in PER3 and a novel nominally significant association between diurnal preference and a polymorphism in ARNTL2 PMID: 24635757
39. Five SNPs (rs228727, rs228644, rs228729, rs707467, rs104620202) in the period 3 (PER3) gene are significant correlation with genotype and allele frequency in lung cancer. PMID: 24821610
40. No association with SNPs or haplotypes of the PER3 gene was observed in prophylactic lithium response. PMID: 24636202
41. there is a greater detrimental impact of sleep deprivation in PER3(5/5) than PER3(4/4) carriers. the group with greater attentional performance impairment due to sleep deprivation (PER3(5/5) carriers) is superior at initiating sleep over the 24-h cycle. PMID: 24439663
42. Women with the 4/5 or 5/5 PER3 genotype had a nonstatistically significant 33% increased odds of breast cancer. PMID: 24903750
43. PER3 genotype predicted circadian rhythm period lengthening by lithium, specifically among bipolar disorder cases. PMID: 24150227
44. the association of rs934945 with "morning alertness" and rs2640909 with "morningness". PMID: 23969301
45. there is significant daily variation in PER2, PER3, and ARNTL1 expression with earlier timing of expression in women than in men PMID: 23606611
46. polymorphisms more behaviorally salient with increasing severity and/or duration of sleep restriction PMID: 23171222
47. These data document for the first time that the expression of BMAL1, PER3, PPARD and CRY2 genes is altered in gestational diabetes compared to normal pregnant women. deranged expression of clock genes may play a pathogenic role in GDM. PMID: 23323702
48. Studies indicate that in the cytoplasm, PER3 protein heterodimerizes with PER1, PER2, CRY1, and CRY2 proteins and enters into the nucleus, resulting in repression of CLOCK-BMAL1-mediated transcription. PMID: 23546644
49. Cortisol secretion was modified among police officers with different PER3 VNTR clock gene variants. PMID: 23524621
50. the association study of the 54-nucleotide repeat in exon 18 of the hPer3 gene with a predisposition to opioid dependence among residents of the West Siberian region of Russia PMID: 22976125
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相關疾病：

Advanced sleep phase syndrome, familial, 3 (FASPS3)
亞細胞定位：

Cytoplasm. Nucleus.
數據庫鏈接：

HGNC: 8847

OMIM: 603427

KEGG: hsa:8863

STRING: 9606.ENSP00000355031

UniGene: Hs.162200

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