人**球蛋白A Fc段受体(FcαR/CD89)化学发光**分析试剂盒
基本原理：
本试剂盒采用双抗体夹心法。用抗人FcαR/CD89抗体包被于酶标板上，实验时标本或标准品中的FcαR/CD89会与包被抗体结合，游离的成分被洗去。依次加入生物素化的抗人FcαR/CD89抗体和辣根过氧化物酶标记的亲和素。抗人FcαR/CD89抗体与结合在包被抗体上的人FcαR/CD89结合、生物素与亲和素特异性结合而形成**复合物，游离的成分被洗去。加入发光底物混合液，发光底物在辣根过氧化物酶的催化下发出荧光，用化学发光**分析仪测定化学发光值（RLU），FcαR/CD89浓度与化学发光值之间呈正相关，通过绘制标准曲线求出标本中FcαR/CD89的浓度。
人**球蛋白A Fc段受体(FcαR/CD89)化学发光**分析试剂盒描述：
| 英文名称 | Human FcαR/CD89 (Receptor I for the Fc Fragment of IgA) CLIA Kit | ||
| 中文名称 | 人**球蛋白A Fc段受体(FcαR/CD89)化学发光**分析试剂盒 | ||
| 货号 | KL-H1088c | 种属 | Human/人 |
| 规格 | 96T/Kit (8*12 wells) | ||
| 检测方法 | 双抗体夹心法 | ||
| 检测范围 | 0.156~10ng/mL | 灵敏度 | 0.094ng/mL |
人**球蛋白A Fc段受体(FcαR/CD89)化学发光**分析试剂盒试剂盒组成：
| 中文名称 | 英文名称 | 规格 | 保存 |
| CLIA酶标板 | Micro CLIA Plate | 8×12 wells | 4℃/-20℃ # |
| 冻干标准品 | Reference Standard | 2 支 | 4℃/-20℃ # |
| 标准品&样品稀释液 | Reference Standard & Sample Diluent | 1瓶 20mL | 4℃ |
| 浓缩生物素化抗体 | Concentrated Biotinylated Detection Ab | 1支 120μL | 4℃/-20℃ # |
| 生物素化抗体稀释液 | Biotinytated Detection Ab Diluent | 1瓶10mL | 4℃ |
| 浓缩HRP酶结合物 | Concentrated HRP Conjugate | 1支 120μL | 4℃(避光) |
| 酶结合物稀释液 | HRP Conjugate Diluent | 1瓶 10mL | 4℃ |
| 浓缩洗涤液（25×） | Concentrated Wash Buffer (25×) | 1瓶 30mL | 4℃ |
| 发光底物A液 | Substrate Reagent A | 1瓶 5mL | 4℃(避光) |
| 发光底物B液 | Substrate Reagent B | 1瓶 5mL | 4℃(避光) |
| 封板覆膜 | Plate Sealer | 5 张 | |
| 产品说明书 | Manual | 1 份 | |
| 质检报告 | Certificate of Analysis | 1 份 | |
| 特别说明： #: 一周内使用可存于4℃，需长时间存放或多次使用建议存于-20℃. |
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1.在各孔中加入标准品或样品各 100μL，37℃孵育90分钟
2. 倒去孔内液体，拍干，加入 100μL 生物素化抗体工作液，37℃孵育 60 分钟
3. 洗涤 3 次
4. 加入 100μL 酶结合物工作液， 37℃孵育 30 分钟
5. 洗涤 5 次
6. 加入 100μL 发光底物混合液， 37℃孵育 5 分钟左右
7. 立即测定各孔的化学发光值
8. 结果计算
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