Recombinant Human Pro-neuropeptide Y (NPY)
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货号:CSB-YP016034HU
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规格:
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来源:Yeast
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其他:
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货号:CSB-EP016034HU
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规格:
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来源:E.coli
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其他:
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货号:CSB-EP016034HU-B
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规格:
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来源:E.coli
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共轭:Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
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其他:
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货号:CSB-BP016034HU
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规格:
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来源:Baculovirus
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其他:
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货号:CSB-MP016034HU
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规格:
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来源:Mammalian cell
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其他:
产品详情
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纯度:>85% (SDS-PAGE)
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基因名:
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Uniprot No.:
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别名:C-flanking peptide of NPY; CPON; Neuropeptide tyrosine; Neuropeptide Y precursor; NPY; NPY_HUMAN; Pro neuropeptide Y; PYY 4; PYY4; Y Neuropeptide
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种属:Homo sapiens (Human)
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蛋白长度:Partial
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表达区域:29-64
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氨基酸序列YP SKPDNPGEDA PAEDMARYYS ALRHYINLIT RQRY
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蛋白标签:Tag type will be determined during the manufacturing process.
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially. -
产品提供形式:Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand. -
复溶:We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
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储存条件:Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
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保质期:The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C. -
货期:Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
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注意事项:Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
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Datasheet :Please contact us to get it.
相关产品
靶点详情
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功能:NPY is implicated in the control of feeding and in secretion of gonadotrophin-release hormone.
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基因功能参考文献:
- Neuropeptide Y (NPY) is a pleiotropic gene implicated in stress resilience and is associated with higher levels of conscientiousness. Along with environmental factors such as stressful life events, this gene may be a factor in the neurobiology of human personality. PMID: 29494882
- We found the suicide-associated gene coexpression network. The reconstructed network consisted of 104 genes. Topological analysis showed that in total, CCK, INPP1, DDC, and NPY genes are the most fundamental hubs in the network. PMID: 29381655
- Data indicated that NPY plays a protective role in ER stress-induced neuronal cell death through activation of the PI3K-XBP1 pathway. PMID: 29650257
- This study provided proof that SNPs within NPY is significantly associated with the susceptibility to and the prognosis of cervical vertigo. PMID: 29197114
- Data suggest that up-regulation of NPY inhibits proliferation of adipose-derived stem cells while promoting adipogenesis and up-regulating expression of white adipocyte biomarkers PPARG, CEBPA, CIDEC, and RIP140. (PPARG = peroxisome proliferator activated receptor gamma; CEBPA = CCAAT/enhancer-binding protein alpha; CIDEC = cell death-inducing DFFA-like effector C; RIP140 = nuclear receptor interacting protein 1) PMID: 28954935
- results are the first to demonstrate that functional NPY variation alters chronic stress-related vagal control, suggesting a potential parasympathetic role for NPY gene in stress regulation PMID: 27527739
- Medium chain triglyceride nutritional supplementation increased the amount of activated ghrelin and NPY in anorexia nervosa patients. PMID: 28361739
- Analysis indicates that low levels of NPY in psychogenic non-epileptic seizure patients may confer greater vulnerability to exhibit seizure-like symptoms and lower quality of life. PMID: 28927333
- The rs16147 genotype affected the reduction in insulin resistance and insulin levels in response to two different hypocaloric diets in obese subjects, with a lack of response in subjects with the major allele. PMID: 28787737
- We found that the NPY gene rs16147 SNP was related to the change in insulin levels, homeostasis model assessment-insulin resistance, CRP, IL-6 and waist circumference at 3 months after a hypocaloric low-fat diet. PMID: 27599771
- genetic variation in NPY and NPY2R is at low frequency and thus does not make a major contribution to the obese phenotype in the general population PMID: 28857123
- Genetic risk score (GRSNPY) analysis found twelve significant (P<0.05) serum NPY concentration related SNPs among alpha7 nicotinic acetylcholine receptor gene CHRNA7, insulin receptor gene INSR, leptin receptor gene LEPR, glucocorticoid receptor (GR) gene NR3C1, and NPY gene. However, after permutation test of gene score the predictive value of GRSNPY remained non-significant (P=0.078). CONCLUSIONS: Serum NPY level ... PMID: 27837667
- In obese males, the rs164147 polymorphism of the NPY gene is associated with leptin, insulin level, HOMA-IR, and an increased risk of MetS and its related phenotypes, such as central obesity and hyperglycemia. PMID: 27788523
- Both structural (+1128T/C) and promoter polymorphisms (-399 T/C) of Neuropeptide Y are strongly associated with type-II diabetes susceptibility in Gujarat population which at least in part, may result in higher levels of Neuropeptide Y thereby suggesting its crucial role in type-II diabetes susceptibility. PMID: 27749914
- Hypermethylation of WIF1 (WNT inhibitory factor 1) and NPY (neuropeptide Y) genes was significantly higher in tumor tissue compared to normal tissue, independently of tumor stage. PMID: 27251038
- Our results provided clinical evidences for NPY participating in the bone healing process in a nonhypothalamic manner, most probably by directly promoting osteogenesis of mesenchymal stem cells. PMID: 27720230
- In conclusion, the obtained results demonstrate the probable role of NPY SNPs in susceptibility to multiple sclerosis within the Iranian population. PMID: 27559040
- Neuropeptide Y is the best dipeptidyl peptidase 4 (DPP4)-substrate in blood, being truncated by soluble and membrane DPP4, respectively. The decline of soluble DPP4 in acute depression could be reversed upon anti-depressive treatment. PMID: 26988064
- The CT genotype of rs5574 and the GT genotype of rs17149106 are significantly associated with prevalent asthma. PMID: 27469060
- study implicates NPY as a potential target in antihypertensive therapies for preeclampsia patients PMID: 26431933
- NPY is efficiently cleaved by FAP indicating a potential function for FAP in neuropeptide regulation within liver and cancer biology. PMID: 26621486
- NPY plays important roles in the pathogenesis and pathophysiology of pituitary adenomas, as shown in this clinical study. PMID: 26683132
- NPY levels were higher in both obese and non-obese PCOS patients compared to healthy controls. PMID: 26291814
- minor autoantigen in children with newly diagnosed type 1 diabetes PMID: 25258030
- s observed that NPY levels were decreased in two Machado-Joseph disease patients' cerebella. PMID: 26220979
- Suggest IL-4 as marker of allergic airway inflammation in asthma, and roles for adiponectin and neuropeptide Y in neurohormonal signaling. PMID: 26111352
- This study suggests that NPY rs16147 T and rs16139 C minor alleles are associated with increased risk, whereas the minor allele T of the rs5574 is associated with a reduced risk of obesity. PMID: 26240981
- NPY expression is increased during atherogenesis and in particular in unstable plaques PMID: 24858338
- Immunohistochemical distribution of this peptide in the epidermal skin (from abdomen, breast and face) of healthy women was analysed. PMID: 26002416
- The C-terminal alpha-helix of Neuropeptide Y, which is formed in a membrane environment in the absence of the receptor, is unwound starting at T(32) to provide optimal contacts in a binding pocket within the transmembrane bundle of the NPY-Y2 receptor. PMID: 25924821
- Data suggest that nutritional status and up-regulation of NPY in cerebrospinal fluid are related to disease progression in adults with chronic kidney disease (CKD); up-regulation of serum NPY levels may predict risk of cardiovascular events in CKD. PMID: 25920420
- in AN patients, the NPY system is not up-regulated by chronic undernutrition suggesting that this may play a role in the inability of anorectic women to adapt food intake to their energy demand. PMID: 25798605
- The mean neuropeptide-Y level was 62.29 +/- 13.89 pg/mL in the breath-holding spells group and 58.24 +/- 12.30 pg/mL in the control group. PMID: 26021463
- neuropeptide Y has a role in Ewing sarcoma bone invasion PMID: 25714031
- study is the first to observe a sexually dimorphic role of alleles at NPY in humans and support previous genome-wide findings of a role of NPY in severe PD. PMID: 25256105
- Data suggest that an SNP in NPY (rs16147) is associated with change in abdominal adiposity in subjects with central obesity in response to dietary interventions (low/high fat); T allele carriers on high-fat diet regained abdominal fat. PMID: 26156739
- The data are in line with the hypothesis that NPY signaling is altered in affective disorders and states of emotional dysregulation. PMID: 25453484
- The rs16147 polymorphism may be associated with presence of metabolic syndrome (MetS) among subjects with documented coronary artery disease (CAD). Carriage of NPY A allele in patients with CAD is associated with a higher prevalence of MetS. PMID: 24897239
- This study suggests that the rs16147 polymorphism in the NPY gene may not be a potential contributor to the risk of CAD in an Iranian population. PMID: 25427865
- relationship existed between serum NPY and depressive disorders, posttraumatic stress disorder, and resilience. PMID: 24709369
- NPY may be a possible contributor to metabolic syndrome and associated cancer for the Han ethnic group. PMID: 25081719
- Distribution of peptidergic populations in the human dentate gyrus (somatostatin [SOM-28, SOM-12] and neuropeptide Y [NPY]) during postnatal development. PMID: 24965867
- Polymorphisms within NPY are associated with vitiligo susceptibility. PMID: 25221996
- A putative mechanism based on NPY-induced inhibition of voltage-dependent Ca(2+) influx in pre- and post-synaptic neurons is proposed. PMID: 25026432
- Systemic NPY levels are elevated in patients with Ewing sarcoma, and these high levels are associated with unfavorable disease features. PMID: 25387699
- NPY and its Y receptor are possible mediators of both vasoconstriction and pulmonary vascular remodelling in pulmonary hypertension PMID: 24779394
- Study demonstrated an interaction of NPY genotype and childhood emotional maltreatment on amygdala and posterior cingulate cortex activation during processing of emotional faces, in addition to a faster behavioral response PMID: 23482625
- In a series of human fetuses, neuropeptide Y-containing nerve fibers was present and could be detected as early as in the pineal of four- to five-month-old fetuses. PMID: 24757681
- BIBP-3226 was used to antagonize Y(1)-receptors, NPY to test the efficacy of the antagonism. PMID: 24213859
- Neuropeptide Y has fungicidal, antimicrobial activity against Candida albicans. PMID: 9756788
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亚细胞定位:Secreted. Cytoplasmic vesicle, secretory vesicle, neuronal dense core vesicle.
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蛋白家族:NPY family
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组织特异性:One of the most abundant peptides in the nervous system. Also found in some chromaffin cells of the adrenal medulla.
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数据库链接:
HGNC: 7955
OMIM: 162640
KEGG: hsa:4852
STRING: 9606.ENSP00000242152
UniGene: Hs.1832
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