Exendin-4 ELISA试剂盒(ab272192)
Key features and details
- One-wash 90 minute protocol
- Sensitivity: 2.58 pg/ml
- Range: 11.72 pg/ml - 750 pg/ml
- Sample type: Cell culture media
- Detection method: Colorimetric
- Assay type: Sandwich (quantitative)
概述
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产品名称
Exendin-4 ELISA试剂盒 -
检测方法
Colorimetric -
精确度
批次内 样品 n Mean SD CV% Supernatant 8 6.1% 批次间 样品 n Mean SD CV% Supernatant 3 1.9% -
样品类型
Cell culture media -
检测类型
Sandwich (quantitative) -
灵敏度
2.58 pg/ml -
范围
11.72 pg/ml - 750 pg/ml -
回收率
特定样本回收率 样品类型 平均% 范围 Cell culture media 115 113% - 118% -
检测时间
1h 30m -
实验步骤
One step assay -
产品概述
Exendin-4 ELISA kit (ab272192) is a single-wash 90 min sandwich ELISA designed for the quantitative measurement of Exendin-4 protein in cell culture media. It uses our proprietary SimpleStep ELISA® technology. Quantitate Exendin-4 with 2.58 pg/mL sensitivity.
SimpleStep ELISA® technology employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our SimpleStep ELISA® plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time. See the SimpleStep ELISA® protocol summary in the image section for further details. Our SimpleStep ELISA® technology provides several benefits:
-Single-wash protocol reduces assay time to 90 minutes or less
-High sensitivity, specificity and reproducibility from superior antibodies
-Fully validated in biological samples
-96-wells plate breakable into 12 x 8 wells strips
A 384-well SimpleStep ELISA® microplate (ab203359) is available to use as an alternative to the 96-well microplate provided with SimpleStep ELISA® kits.
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说明
Exendin-4 is a 39 amino acid peptide found in venom from the Gila monster Helicoderma suspectum. Exendin-4 is a member of the glucagon secretin family of peptide hormones and neuropeptides. The venom protein mimics the incretin hormone glucagon-like peptide 1 (GLP-1) and stimulates insulin synthesis and secretion, protects against beta-cell apoptosis in response to different insults, and promotes beta-cell proliferation. Exendin-4 also promotes satiety, reduces food intake, fat deposition and body weight. It also is known to inhibit gastric emptying. Exendin-4 interactions with GLP-1 receptor (GLP1R). induces hypotension that is mediated by relaxation of cardiac smooth muscle.
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经测试应用
适用于: Sandwich ELISAmore details -
平台
Pre-coated microplate (12 x 8 well strips)
性能
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存放说明
Store at +4°C. Please refer to protocols. -
组件 1 x 96 tests 10X Exendin-4 Capture Antibody 1 x 600µl 10X Exendin-4 Detector Antibody 1 x 600µl 10X Wash Buffer PT (ab206977) 1 x 20ml Antibody Diluent 4BI 1 x 6ml Exendin-4 Lyophilized Recombinant Protein 2 vials Plate Seal 1 unit Sample Diluent NS (ab193972) 1 x 12ml SimpleStep Pre-Coated 96-Well Microplate (ab206978) 1 unit Stop Solution 1 x 12ml TMB Development Solution 1 x 12ml -
研究领域
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相关性
Exendin 4 is a 39 amino acid peptide found in venom from the Gila monster Helicoderma suspectum. It is a member of the glucagon secretin family of peptide hormones and neuropeptides. Exendin 4 is a potent agonist of the GLP1 receptor and hence a potent stimulator of insulin secretion. -
细胞定位
Secreted -
别名
- Exenatide
- Exendin4
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab272192于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
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Sandwich ELISA |
Use at an assay dependent concentration.
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说明 |
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Sandwich ELISA
Use at an assay dependent concentration. |
图片
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SimpleStep ELISA technology allows the formation of the antibody-antigen complex in one single step, reducing assay time to 90 minutes. Add samples or standards and antibody mix to wells all at once, incubate, wash, and add your final substrate. See protocol for a detailed step-by-step guide.
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The Exendin-4 standard curve was prepared as described in Section 10. Raw data values are shown in the table. Background-subtracted data values (mean +/- SD) are graphed.
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Interpolated concentrations of spiked* Exendin-4 RPMI-1640 cell culture media +/- 10% FBS samples.
数据表及文件
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SDS download
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Datasheet download
文献 (0)
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