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中文名称:大鼠羟脯氨酸(Hyp)酶联免疫试剂盒
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货号:CSB-E08838r
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规格:96T/48T
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价格:¥3900/¥2500
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其他:
产品详情
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产品描述:CUSABIO专为大鼠样本设计的羟脯氨酸(Hyp)定量检测试剂盒,采用竞争性酶联免疫吸附法,适用于血清、血浆及组织匀浆样本的科研分析。羟脯氨酸是胶原蛋白的重要组成成分,其含量可反映胶原代谢水平,在纤维化疾病机制研究、组织修复评估及骨代谢调控等领域具有重要科研价值。试剂盒检测灵敏度为0.156 ng/mL,线性范围为0.156-10 ng/mL,通过预包被抗体与样本中Hyp竞争结合生物素标记检测物,结合链霉亲和素-HRP系统显色,最终根据标准曲线计算目标浓度。该试剂盒操作便捷,可高效检测大鼠模型(如肝纤维化、肺纤维化)中胶原沉积程度,或用于皮肤创伤修复、骨关节炎等研究中的组织代谢动态监测,为探索Hyp相关分子机制提供可靠工具。
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缩写:Hyp
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种属:Rattus norvegicus (Rat)
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样本类型:serum, plasma, tissue homogenates
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检测范围:0.156 ng/mL-10 ng/mL
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灵敏度:0.078 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:Competitive
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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 rat Hyp 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) 1:200 Average % 87 Range % 83-90 1:400 Average % 94 Range % 90-98 1:800 Average % 101 Range % 97-104 1:1600 Average % 96 Range % 93-99 -
回收率:
The recovery of rat Hyp 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 89-98 EDTA plasma (n=4) 100 95-105 -
标准曲线:
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed. ng/ml OD1 OD2 Average 10 0.112 0.115 0.114 5 0.186 0.179 0.183 2.5 0.260 0.269 0.265 1.25 0.471 0.439 0.455 0.625 0.615 0.629 0.622 0.312 1.117 1.139 1.128 0.156 2.173 2.229 2.201 0 2.854 2.897 2.876 -
数据处理:
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货期:3-5 working days
引用文献
- Chamomile fowers extract protects against thinner inhalation-induced lung toxicity via attenuating cytochrome P2E1 activity, surfactant defciency, and alveolar structural injury in rats AM Elgharieb, AM El_x001e_Wakf, AE Abdrabouh-Beni,Beni-Suef University Journal of Basic and Applied Sciences,2024
- Sorafenib and edaravone protect against renal fibrosis induced by unilateral ureteral obstruction via inhibition of oxidative stress, inflammation, and RIPK-3/MLKL pathway MA Abou Taha,NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,2024
- Regulation of miRNA-155-5p ameliorates NETosis in pulmonary fibrosis rat model via inhibiting its target cytokines IL-1β, TNF-α and TGF-β1 RM Adel,International immunopharmacology,2024
- Protective effects of Silibinin and cinnamic acid against paraquat-induced lung toxicity in rats: impact on oxidative stress, PI3K/AKT pathway and miR-193a signaling BM Fouad,/,2024
- Betanin protects against bleomycin-induced pulmonary fibrosis by regulating the NLRP3/IL-1β/TGF-β1 pathway-mediated epithelial-to-mesenchymal transition NA Abd Elrazik,Food & function,2023
- Effects of novel Fufang Biejia Ruangan Tablets with sheep placenta as substitute for Hominis Placenta on CCl4-induced liver fibrosis B Shen,Chinese Herbal Medicines,2023
- Sunitinib displays pulmonary fibrosis in experimental rats: Role of IL-17A dependent pathway ME Asker,International immunopharmacology,2023
- Inflammatory and proapoptotic effects of inhaling gasoline fumes on the lung and ameliorative effects of fenugreek seeds AE Abdrabouh,Scientific reports,2022
- Combined Lycium barbarum polysaccharides and C-phycocyanin increase gastric Bifidobacterium relative abundance and protect against gastric ulcer caused by aspirin in rats Shu-Yu Hsieh,Nutrition & Metabolism,2021
- Gastroprotective effect of Lycium barbarum polysaccharides and C-phyocyanin in rats with ethanol-induced gastric ulcer YZ Lian,International Journal of Biological Macromolecules,2020
- A Compound of Chinese Herbs Protects against Alcoholic Liver Fibrosis in Rats via the TGF-β1/Smad Signaling Pathway Xiaomeng Li,Evidence-Based Complementary and Alternative Medicine,2019
- Evaluation of dipeptidyl peptidase-4 enzyme inhibition by some commonly used gliptins on cutaneous wound healing in albino rats Chandrashekar K.et al,National Journal of Physiology, Pharmacy and Pharmacology,2017
- Effect of a new cross-linked hyaluronan gel on the staple line after sleeve gastrectomy in a rat model Blbller N.et al,Acta Cir Bras,2018
- Abrogation of carbon tetrachloride-induced hepatotoxicity in Sprague-Dawley rats by Ajwa date fruit extract through ameliorating oxidative stress and apoptosis. Elsadek B.et al,Pak J Pharm Sci,2017
- Protective effects of pterostilbene against acetaminophen-induced hepatotoxicity in rats El-Sayed el-SM.et al,J Biochem Mol Toxicol.,2015
- Effects of long-term ethanol administration in a rat total enteral nutrition model of alcoholic liver disease /,Liver and Biliary Tract,2011
- improving the angiogenic potential of collagen matrices by covalent incorporation of astragalus polysaccharides /,International Journal of Burns and Trauma,2011
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相关问答
Please let us know if it can be used with bone extract sample.
Usually we suggest you test the sample types mentioned in the kit manual. You can do a pretest first if you want to test bone extract sample.
We are interested in sourcing Human, mouse, rat hydroxyproline,Hyp ELISA Kit from CusaBio. What would be our purchasing price for it?
Also, can you kindly clarify why they are a species specific elisa kit while hydroxyproline is a small molecule?
I will ask our distributor in your area to give you a quote by email.
Hydroxyproline is small molecule and it is the same in different species. There are 3 reasons why we have species specific elisa kits.
1. For different species, the sample matrix is different and the characteristics of antibody used in the kits are also different.
2. The methods of these 3 kits are different. Human kit and mouse kit are based on double antibody sandwich method.
When the kit was developed, it was designed to mimic the presence of hydroxyproline in vivo. It can detect polymerized form. (including the polymerized form with other proteins and self-polymerization form). For human kit, capture antibody is mouse monoclonal antibody and detection antibody is goat polyclonal antibody; For mouse kit, capture antibody is rat monoclonal antibody and detection antibody is goat polyclonal antibody.
Rat kit is based on competitive method. The plate is coated with mouse monoclonal antibody. HRP conjugated HYP competes with the HYP in the sample. The kit can detect the endogenous total HYP, including free form and polymerized form.
3. The reason why different kits use different methods is based on a variety of factors. You can choose the appropriate kit to avoid matrix problems.
Pls let me know if you have any further questions. Thank you.
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