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中文名称:人精氨基琥珀酸合成酶1(ASS1)酶联免疫试剂盒
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货号:CSB-EL002234HU
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规格:96T/48T
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价格:¥3600/¥2500
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其他:
产品详情
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产品描述:
This Human ASS1 ELISA Kit was designed for the quantitative measurement of Human ASS1 protein in serum, plasma, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 7.8 pg/mL-500 pg/mL and the sensitivity is 1.95 pg/mL.
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别名:Argininosuccinate synthase 1 ELISA Kit; Argininosuccinate synthase ELISA Kit; Argininosuccinate synthetase 1 ELISA Kit; ASS ELISA Kit; Ass-1 ELISA Kit; ass1 ELISA Kit; ASSA ELISA Kit; ASSY_HUMAN ELISA Kit; Citrulline aspartate ligase ELISA Kit; Citrulline--aspartate ligase ELISA Kit; CTLN1 ELISA Kit
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缩写:ASS1
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Uniprot No.:
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种属:Homo sapiens (Human)
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样本类型:serum, plasma, tissue homogenates
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检测范围:7.8 pg/mL-500 pg/mL
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灵敏度:1.95 pg/mL
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反应时间:1-5h
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样本体积:50-100ul
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检测波长:450 nm
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研究领域:Metabolism
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测定原理:quantitative
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测定方法:Sandwich
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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 ASS1 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 % 92 Range % 86-97 1:2 Average % 97 Range % 92-105 1:4 Average % 85 Range % 81-88 1:8 Average % 89 Range % 83-94 -
回收率:
The recovery of human ASS1 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) 91 87-95 EDTA plasma (n=4) 99 95-104 -
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 500 2.912 3.021 2.967 2.831 250 2.380 2.500 2.440 2.304 125 1.689 1.675 1.682 1.546 62.5 0.964 0.889 0.927 0.791 31.2 0.581 0.603 0.592 0.456 15.6 0.428 0.412 0.420 0.284 7.8 0.276 0.278 0.277 0.141 0 0.136 0.135 0.136 -
数据处理:
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货期:3-5 working days
引用文献
相关产品
靶点详情
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功能:One of the enzymes of the urea cycle, the metabolic pathway transforming neurotoxic amonia produced by protein catabolism into inocuous urea in the liver of ureotelic animals. Catalyzes the formation of arginosuccinate from aspartate, citrulline and ATP and together with ASL it is responsible for the biosynthesis of arginine in most body tissues.
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基因功能参考文献:
- In ASS1-knockout cells, DEPTOR, an inhibitor of mTORC1 signal, was downregulated and mTORC1 signaling was more activated in response to arginine. PMID: 28358054
- Results indicate that the reduced ASS1 expression in Dox-resistant sarcomas may contribute to drug resistance in association with the expression of P-glycoprotein. PMID: 27683125
- Cisplatin-induced synthetic lethality to arginine-starvation therapy by transcriptional suppression of ASS1 is regulated by DEC1, HIF-1alpha, and c-Myc transcription network and is independent of ASS1 promoter DNA methylation. PMID: 27765932
- Low expression of ASS1 is associated with glioblastoma. PMID: 27431689
- defined a new hepatocellular adenoma subgroup at a high risk of bleeding PMID: 28646562
- ASS1 acetylation by CLOCK exhibits circadian oscillation in human cells and mouse liver, possibly caused by rhythmic interaction between CLOCK and ASS1, leading to the circadian regulation of ASS1 and ureagenesis. PMID: 28985504
- update reports 137 mutations in the ASS1 gene (64 of which are novel), consisting of 89 missense mutations, 19 nonsense mutations, 17 mutations that affect splicing, and 12 deletions; the change p.Gly390Arg is by far the most common mutation and is widely spread throughout the world PMID: 28111830
- Of 21 ASS potential kinetic mutations, 13 were totally inactive while 8 exhibited decreased affinity for aspartate and citrulline. PMID: 27287393
- Low ASS1 expression was associated with higher recurrence , shorter disease-free survival and shorter overall survival in patients with pancreatic ductal adenocarcinoma. PMID: 28187218
- The s showed that ASS1 mutations linked to type I citrullinemia disrupt the ASS1-PRMT7 interaction, which might explain the molecular pathogenesis of the disease. PMID: 28587924
- Identification of three novel CTLN1 mutations in fourteen patients with citrullinemia type 1 has been reported. PMID: 28132756
- In this trial, arginine deprivation with ADI-PEG20 improved PFS in patients with ASS1-deficient mesothelioma. Targeting arginine is safe and warrants further clinical investigation in arginine-dependent cancers. PMID: 27584578
- combining hypoxia and ADI-PEG20 synergistically inhibited ASS1. PMID: 26972697
- ASS1 genomic variants (rs10901080 and rs10793902) can serve as pharmacogenomic biomarkers to predict hydroxyurea treatment efficacy in sickle cell disease/beta-thalassemia compound heterozygous patients. PMID: 26895070
- results show that ASS1 is elevated at the mRNA and protein levels in mesothelioma 3D spheroids and in human pleural mesotheliomas. We also have uncovered a survival role for ASS1 PMID: 26982031
- results demonstrate that ASS1 downregulation is a novel mechanism supporting cancerous proliferation, and they provide a metabolic link between the urea cycle enzymes and pyrimidine synthesis PMID: 26560030
- More than 50 % of the high-grade pulmonary neuroendocrine carcinomas tested lack immunohistochemically detectable ASS, suggesting that they are auxotrophic for arginine and potential candidates for arginine deprivation therapy. PMID: 25548129
- Three novel splicing and missense mutations have been identified in the ASS1 gene in classical citrullinemia patients. PMID: 25179242
- ASS expression in gastric cancer was associated with a poor prognosis. PMID: 25333458
- we reviewed the English literature on mutations in the ASS and SLC25A13 genes, and their genotype-phenotype correlations to provide valuable insights into the molecular genetic background of citrullinemia--{REVIEW} PMID: 24508627
- Data indicate that argininosuccinate synthetase 1 (ASS1) abundance is a prognostic factor for overall breast cancer survival. PMID: 24692592
- Argininosuccinate synthetase gene is silenced by CpG methylation in children with phenylketonuria.The promoter of argininosuccinate synthetase was methylated which silence the transcription of argininosuccinate synthetase. PMID: 24192130
- Aberrant loss of ASS1 strongly links to DNA methylation in neck nodal metastases of NPC and significantly correlates with advanced T classification, and independently predicts worse DSS and DMFS in independent NPC tissue specimens. PMID: 23897555
- Together with the observation that AS1 protein and mRNA levels decrease during wild-type infection, this work suggests that reduced AS1 activity is partially responsible for the metabolic program induced by infection. PMID: 24297925
- Our findings highlight ASS1 as a novel tumor suppressor in myxofibrosarcomas, with loss of expression linked to promoter methylation, clinical aggressiveness, and sensitivity to ADI-PEG20. PMID: 23549872
- ASS expression is decreased significantly in hepatocellular carcinoma tissues. PMID: 23339388
- Mutations are identified only in exons of ASS1 gene from the Korean patients with citrullinemia type I. PMID: 23099195
- The present study demonstrated a key regulatory role of KLF4 in the endothelial ASS1 expression and NO production in response to laminar shear stress. PMID: 22430140
- The ASS release represents a potential counteracting liver reaction to LPS. PMID: 21481813
- the expression of ASS1 harmonized with that of NOS3 may be important for the optimized endothelial NO production and the prevention of the inflammatory monocyte adhesion to endothelial cells. PMID: 21106532
- Analysis of five SNPs of the ASS1 gene revealed that the G allele of rs7860909 is associated with increased CL/P risk. PMID: 20739017
- In patients with osteosarcoma, reduced expression of ASS is not only a novel predictive biomarker for the development of metastasis, but also a potential target for pharmacologic intervention. PMID: 20159990
- Studies indicate that the proximal region of the AS promoter contains an E-box that is recognized by c-Myc and HIF-1alpha and a GC-box by Sp4. PMID: 19934275
- Mutational analysis revealed three alleles with a common mutation and five new mutations. PMID: 11708871
- structure and use in diagnosing citrullinemia PMID: 11941481
- Sixteen novel mutations have been identified in the argininosuccinate synthetase gene in citrullinemia patients. PMID: 12815590
- argininosuccinate synthetase gene expression is stimulated by glutamine through cytosolic O-glycosylation of Sp1 in tumor cells PMID: 14570901
- Argininosuccinate synthetase has a role in preventing autotoxicity from nitric oxide overproduction PMID: 15192091
- Extensive mutation study by direct genomic sequencing of ASS demonstrated a homozygous G117S mutation in one patient and homozygous R363W mutations in the other two families PMID: 16124451
- IL-1beta induces nitric oxide which has antagonistic effects on argininosuccinate synthetase gene and on the activity of argininosuccinate synthetase PMID: 16380201
- ASS, the c-myc-regulated gene is involved in genotype-C-HBV-related HCC, suggesting that c-myc is related to the hepatocarcinogenic activity of genotype-C HBV. PMID: 16703398
- Low argininosuccinate synthetase is associated with renal cell carcinoma PMID: 17096330
- high levels of AS expression, which may be required for several arginine-dependent processes in cancer, including the production of nitric oxide, proline, pyrimidines and polyamines, is regulated by TNF-alpha PMID: 17354225
- HSCARG regulation of argininosuccinate synthetase activity is crucial for maintaining the intracellular balance between redox state and nitric oxide levels PMID: 18263583
- These results show that liver-specific enhancement of ASS gene expression is mediated in part by the cAMP signaling pathway through a distal CRE site. PMID: 18840401
- argininosuccinate synthetase behaves as a typical suckling enzyme because its expression all but disappears in the putative weaning period of human infants. PMID: 19000307
- a survey of the correlation between mutations in the ASS1 gene and the respective clinical courses of citrullinemia type I as described so far (Review) PMID: 19006241
- The studied families showed the same mutation: ASS~p.G390R, associated with the early-onset/severe phenotype. PMID: 19358837
- changes in gene expression are induced by laminar shear stress as well as by cellular senescence PMID: 19409979
- Epigenetic silencing of argininosuccinate synthetase confers resistance to platinum-induced cell death but collateral sensitivity to arginine auxotrophy in ovarian cancer. PMID: 19533750
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相关疾病:Citrullinemia 1 (CTLN1)
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亚细胞定位:Cytoplasm, cytosol.
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蛋白家族:Argininosuccinate synthase family, Type 1 subfamily
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组织特异性:Expressed in adult liver.
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数据库链接:
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