Human Prokineticin-2(PROK2) ELISA kit
-
中文名称:人前动力蛋白2(PROK2)酶联免疫试剂盒
-
货号:CSB-EL018747HU
-
规格:96T/48T
-
价格:¥3600/¥2500
-
其他:
产品详情
-
产品描述:
This Human PROK2 ELISA Kit was designed for the quantitative measurement of Human PROK2 protein in serum, plasma, cell culture supernates, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 6.25 pg/mL-400 pg/mL and the sensitivity is 1.56 pg/mL.
-
别名:BV8 ELISA Kit; Bv8 homolog ELISA Kit; MIT1 ELISA Kit; PK2 ELISA Kit; PROK2 ELISA Kit; PROK2_HUMAN ELISA Kit; Prokineticin-2 ELISA Kit; Protein Bv8 homolog ELISA Kit
-
缩写:PROK2
-
Uniprot No.:
-
种属:Homo sapiens (Human)
-
样本类型:serum, plasma, cell culture supernates, tissue homogenates
-
检测范围:6.25 pg/mL-400 pg/mL
-
灵敏度:1.56 pg/mL
-
反应时间:1-5h
-
样本体积:50-100ul
-
检测波长:450 nm
-
研究领域:Neuroscience
-
测定原理:quantitative
-
测定方法:Sandwich
-
精密度:
Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess. Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess. -
线性度:
To assess the linearity of the assay, samples were spiked with high concentrations of human PROK2 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay. Sample Serum(n=4) 1:1 Average % 97 Range % 91-104 1:2 Average % 88 Range % 86-91 1:4 Average % 99 Range % 85-106 1:8 Average % 95 Range % 89-98 -
回收率:
The recovery of human PROK2 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section. Sample Type Average % Recovery Range Serum (n=5) 94 89-97 EDTA plasma (n=4) 98 93-105 -
标准曲线:
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. pg/ml OD1 OD2 Average Corrected 400 2.345 2.245 2.295 2.160 200 1.764 1.664 1.714 1.579 100 1.112 1.102 1.107 0.972 50 0.713 0.693 0.703 0.568 25 0.422 0.412 0.417 0.282 12.5 0.305 0.295 0.300 0.165 6.25 0.212 0.202 0.207 0.072 0 0.135 0.134 0.135 -
数据处理:
-
货期:3-5 working days
相关产品
靶点详情
-
功能:May function as an output molecule from the suprachiasmatic nucleus (SCN) that transmits behavioral circadian rhythm. May also function locally within the SCN to synchronize output. Potently contracts gastrointestinal (GI) smooth muscle.
-
基因功能参考文献:
- The results indicate that PK2 over-production perpetuates psoriatic symptoms by creating PK-2-IL-1 vicious loop. PK2 is a central player in psoriasis and a promising psoriasis-specific target. PMID: 27887936
- Prokineticin-2 is correlated with various cardiometabolic risk factors. PMID: 26728949
- Data suggest that prokineticins (PROK1 and PROK2) and prokineticin receptors (PROKR1 and PROKR2) act as main regulators of physiological functions of ovary, uterus, placenta, and testis. [REVIEW] PMID: 26574895
- Suggest PROK2 as an angiogenic growth factor in colorectal cancer. PMID: 26317645
- study found a novel mutation in PROK2 in two male siblings presenting normosmic congenital hypogonadotropic hypogonadism, in whom a mutation in the GNRHR gene had been previously described, suggesting the possibility of a digenic inheritance PMID: 25531638
- PROK2 significantly increased in human fetal ovary across gestation. PMID: 26192875
- EG-VEGF, BV8, and PROKR2 gene expression is approximately five, four, and two times higher in cystic fibrosis lungs compared with controls. PMID: 26047640
- No abnormalities were found in the patient group for the PROKR2 and GNRH1genes. In addition, no genomic rearrangements were identified in the healthy control individuals for the described genes PMID: 24002956
- PROK2 signaling in humans is not required for central circadian pacemaker function. PMID: 24423319
- A novel role of BV8 in promoting oncogenesis intrinsic to malignant cells of myeloid origin. PMID: 23548897
- We could not implicate the ligand PROK2 in congenital hypopituitarism and septo-optic dysplasia. PMID: 23386640
- Three PROKR2 mutations previously described in Kallmann syndrome and one new PROK2 mutation were found in patients with isolated congenital anosmia. PMID: 23082007
- Induction of Bv8 expression by granulocyte colony-stimulating factor in CD11b+Gr1+ cells: key role of Stat3 signaling. PMID: 22528488
- Data suggest that elevated prokineticin 2 levels, as a consequence of gastrointestinal tract inflammation, induce visceral pain via prokineticin receptors. PMID: 22050240
- Patients with this genetic form of Kallmann syndrome have been reported to have a possible increased prevalence of obesity and sleep disorders, which may be related to the role of PROK2 in food intake and circadian rhythms (Review) PMID: 20389090
- Review. Role of prokineticins in inflammatory and contractile pathways at parturition in humans. PMID: 20172976
- Male patients carrying biallelic mutations in PROK2 or PROKR2 have a less variable and on average a more severe reproductive phenotype than patients carrying monoallelic mutations in these genes. PMID: 20022991
- Prokineticin 2 transmits the behavioural circadian rhythm of the suprachiasmatic nucleus. PMID: 12024206
- Bv8 and EG-VEGF, along with other factors such as VEGF-A, may maintain the integrity and also regulate proliferation of the blood vessels in the testis PMID: 12604792
- Paracrine role for the PKs and their receptors in endometrial vascular function. PMID: 15126578
- potentially modulates growth, survival, and function of cells of the innate and adaptive immune systems, possibly through autocrine or paracrine signaling mechanisms PMID: 15548611
- study demonstrated that prokineticin 1 and 2 and their receptors are expressed in human prostate and that their levels increased with prostate malignancy PMID: 16763065
- These findings reveal that insufficient prokineticin-signaling through PROKR2 leads to abnormal development of the olfactory system and reproductive axis in man. PMID: 17054399
- Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism PMID: 17959774
- The identification of PROK2 biallelic mutations, that is, a missense mutation, p.R73C, and a frameshift mutation, c.163delA, in two out of 273 patients presenting as sporadic cases, is reported. PMID: 18285834
- PK2/Bv8 expression decreases as the liver evolves towards cancer and does not correlate with HCC angiogenesis PMID: 18300343
- Loss-of-function mutations in PROK2 and PROKR2 underlie both Kallmann syndrome (KS) and normosmic idiopathic hypogonadotropic hypogonadism (IHH). PMID: 18559922
- Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. PMID: 18682503
- no mutations found in Kallmann syndrome PMID: 18723471
- Bv8 expression is regulated by several cytokines in a cell type-specific fashion PMID: 19336519
显示更多
收起更多
-
相关疾病:Hypogonadotropic hypogonadism 4 with or without anosmia (HH4)
-
亚细胞定位:Secreted.
-
蛋白家族:AVIT (prokineticin) family
-
组织特异性:Expressed in the testis and, at low levels, in the small intestine.
-
数据库链接:
Most popular with customers
-
Human Transforming Growth factor β1,TGF-β1 ELISA kit
Detect Range: 23.5 pg/ml-1500 pg/ml
Sensitivity: 5.8 pg/ml
-
-
-
Mouse Tumor necrosis factor α,TNF-α ELISA Kit
Detect Range: 7.8 pg/ml-500 pg/ml
Sensitivity: 1.95 pg/ml
-
-
-
-