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中文名称:人Ⅰ型前胶原N端前肽(PⅠNP)酶联免疫试剂盒
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货号:CSB-E11226h
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规格:96T/48T
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价格:¥3200/¥2500
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其他:
产品详情
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产品描述:CUSABIO人Ⅰ型前胶原N端前肽(PⅠNP)酶联免疫检测试剂盒(货号:CSB-E11226h),通过双抗体夹心法定量检测血清、血浆及组织匀浆样本中的PⅠNP浓度。PⅠNP是Ⅰ型胶原合成过程中的特异性代谢产物,作为骨形成的重要生物标志物,在骨代谢研究、骨质疏松机制探索及骨骼修复药物开发等领域具有重要科研价值。试剂盒检测灵敏度覆盖18.75至1200 pg/mL的线性范围,可精准捕捉样本中微量目标蛋白的动态变化。采用预包被高亲和力捕获抗体的96孔板,通过标准化的酶标二抗显色系统实现稳定检测,实验流程包含样本预处理、孵育、洗涤和读数步骤,配备标准品和对照品确保检测重复性。适用于骨组织工程研究、骨骼疾病动物模型评估、骨代谢相关分子机制解析等科研场景,为骨代谢研究、抗骨质疏松药物筛选及骨再生材料开发提供可靠工具。
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别名:procollagen 1 N-terminal peptide,P1NP,_x000D_ procollagen I N-terminal peptide,PINP
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缩写:PⅠNP
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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:18.75 pg/mL-1200 pg/mL
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灵敏度:4.68 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:Others
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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 PⅠNP 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) 1:100 Average % 97 Range % 89-102 1:200 Average % 90 Range % 83-97 1:400 Average % 99 Range % 94-105 1:800 Average % 96 Range % 90-102 -
回收率:
The recovery of human PⅠNP 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 90-99 EDTA plasma (n=4) 101 95-107 -
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 1200 2.191 2.287 2.239 2.086 600 1.885 1.896 1.891 1.738 300 1.527 1.507 1.517 1.364 150 1.001 1.042 1.022 0.869 75 0.692 0.648 0.670 0.517 37.5 0.499 0.472 0.486 0.333 18.75 0.272 0.288 0.280 0.127 0 0.152 0.154 0.153 -
数据处理:
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货期:3-5 working days
引用文献
- Bone metabolism and inflammatory biomarkers in radiographic and non-radiographic axial spondyloarthritis patients: a comprehensive evaluation I Gómez-García,Frontiers in endocrinology,2024
- Changes in bone turnover markers in patients without bone metastases receiving immune checkpoint inhibitors: An exploratory analysis F Pantano,Journal of bone oncology,2022
- Praeruptorin B inhibits osteoclastogenesis by targeting GSTP1 and impacting on the S-glutathionylation of IKKβ K Xu,Biomedicine & pharmacotherapy,2022
- Three-Dimensional Co-Culture System of Human Osteoblasts and Osteoclast Precursors from Osteoporotic Patients as an Innovative Model to Study the Role of Nutrients: Focus on Vitamin K2 Domitilla Mandatori,Nutrients,2021
- Increasing Vegetable Intake Decreases Urinary Acidity and Bone Resorption Marker in Overweight and Obese Adults: An 8-Week Randomized Controlled Trial JJ Cao,The Journal of nutrition,2021
- TAZ inhibits osteoclastogenesis by attenuating TAK1/NF-κB signaling W Yang,Bone Research,2021
- Citrate Supplementation Restores the Impaired Mineralisation Resulting from the Acidic Microenvironment: An In Vitro Study N Swilam,Nutrients,2020
- Umbilical cord N-terminal procollagen of type l collagen (P1NP) and beta C-terminal telopeptide (βCTX) levels in term pregnancies with vitamin D deficiency M Eraslan Sahin,Journal Gynecological Endocrinology,2020
- Association between bile acid metabolism and bone mineral density in postmenopausal women Zhao YX,Clinics (Sao Paulo),2020
- Dissecting the mechanisms of bone loss in Gorham-Stout disease Michela Rossi, et al,Bone,2019
- Spine bone mineral density increases after 6 months of exclusive lactation, even in women who keep breastfeeding Cooke-Hubley S.et al,Arch Osteoporos,2017
- Physical activity and hypocaloric diet recovers osteoblasts homeostasis in women affected by abdominal obesity Viviana M.et al,Springer US,2016
- Effect of chronic activity-based therapy on bone mineral density and bone turnover in persons with spinal cord injury Astorino TA et al,Eur J Appl Physiol,2013
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