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中文名称:人ADAMTS样蛋白2(ADAMTSL2)酶联免疫试剂盒
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货号:CSB-EL001318HU
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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:人ADAMTS样蛋白2(ADAMTSL2)酶联免疫试剂盒(CSB-EL001318HU)为双抗夹心法ELISA试剂盒,定量检测血清、血浆、组织匀浆样本中的ADAMTSL2含量。ADAMTSL2是一种位于9q34.2的基因,其编码的蛋白质属于ADAMTS(去整合素和金属蛋白酶与血小板反应蛋白基序)家族。该基因在多种生物中保守,其突变与地球物理发育不良有关。研究显示,ADAMTSL2与LTBP4的异常相互作用可能与青少年特发性脊柱侧凸有关,同时,ADAMTSL2蛋白和可溶性生物标记物在识别非酒精性脂肪性肝病(NAFLD)的高危非酒精性脂肪性肝炎和纤维化中具有重要作用。试剂盒检测范围为3.12 ng/mL-200 ng/mL,适用于基础科研中探索ADAMTSL2在发育调控、组织纤维化或代谢性疾病模型中的表达特征。为研究ADAMTSL2在疾病相关信号通路中的作用机制提供可靠工具,特别适用于生物标志物筛选、基因功能验证及病理机制研究等科研场景。本品仅用于科研,不用于临床诊断,产品具体参数及操作步骤详见产品说明书。
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别名:ADAMTS like 2 ELISA Kit; ADAMTS like protein 2 ELISA Kit; ADAMTS-like protein 2 ELISA Kit; ADAMTSL 2 ELISA Kit; ADAMTSL-2 ELISA Kit; ADAMTSL2 ELISA Kit; ATL2_HUMAN ELISA Kit; FLJ45164 ELISA Kit; KIAA0605 ELISA Kit
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缩写:ADAMTSL2
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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:3.12 ng/mL-200 ng/mL
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灵敏度:0.78 ng/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:Signal Transduction
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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 ADAMTSL2 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 % 99 Range % 94-106 1:2 Average % 88 Range % 84-93 1:4 Average % 92 Range % 87-98 1:8 Average % 102 Range % 98-106 -
回收率:
The recovery of human ADAMTSL2 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 87-96 EDTA plasma (n=4) 86 81-92 -
标准曲线:
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. ng/ml OD1 OD2 Average Corrected 200 1.854 1.988 1.921 1.812 100 1.262 1.192 1.227 1.118 50 0.780 0.733 0.757 0.648 25 0.487 0.451 0.469 0.360 12.5 0.312 0.334 0.323 0.214 6.25 0.231 0.217 0.224 0.115 3.12 0.169 0.160 0.165 0.056 0 0.109 0.108 0.109 -
数据处理:
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货期:3-5 working days
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基因功能参考文献:
- CpG-specific DNA methylation of ADAMTSL2 and BTN3A2 at rheumatoid arthritis diagnosis can serve as a marker of treatment response. PMID: 28447857
- Two compound heterozygous mutations were confirmed in the ADAMTSL2 gene of the patient with geleophysic dysplasia. PMID: 28917829
- A novel mutation in ADAMTSL2 (p. Gly421Ser) gene was identified in individuals with Ehlers-Danlos Syndrome. PMID: 26879370
- Two novel homozygous missense mutations in the ADAMTSL2 gene underlie geleophysic dysplasia in two consanguineous families from the United Arab Emirates. PMID: 24014090
- Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia. PMID: 21415077
- These data suggest that ADAMTSL2 mutations may lead to a dysregulation of TGF-beta signaling and may be the underlying mechanism of geleophysic dysplasia. PMID: 18677313
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相关疾病:Geleophysic dysplasia 1 (GPHYSD1)
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亚细胞定位:Secreted.
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数据库链接:
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