CN109142749A - 一种心型脂肪酸结合蛋白检测试剂盒 - Google Patents
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Abstract
本发明公开了一种心型脂肪酸结合蛋白检测试剂盒,包括试剂R1与试剂R2,所述R1试剂包括甘氨酸缓冲液100‑300mmol/L,牛血清白蛋白3‑8mmol/L,巯基乙醇30‑50mmol/L,二硫苏糖醇60‑80mmol/L,黄嘌呤氧化酶1.5‑3.7KU/L,草氨酸钠10‑20mmol/L,氯化钾8‑15mmol/L,所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球20‑35mg/L,甘氨酸缓冲液40‑60mmol/L,牛血清白蛋白2‑6mmol/L,乙二胺四乙酸22‑30mmol/L,甲基异噻唑啉酮15‑28mmol/L,磷酸二氢钾12‑16mmol/L;该心型脂肪酸结合蛋白检测试剂盒能够消除肠型脂肪酸结合蛋白的干扰,并具有反应效果好、检测稳定性能高的特点,大大的提高了使用者的使用检测精确性。
Description
技术领域
本发明涉及一种心型脂肪酸结合蛋白检测试剂盒。
背景技术
心型脂肪酸结合蛋白(hFABP)是心脏中富含的一种新型小胞质蛋白。它具有高度心脏特异性,但在心脏以外的组织中也有低浓度表达。心肌缺血性损伤出现后,hFABP可以早在胸痛发作后1-3小时在血液中被发现,6-8小时达到峰值而且血浆水平在24-30小时内恢复正常。心脏脂肪酸结合胞质蛋白由132个氨基酸组成,分子量为15kDa。心型脂肪酸结合蛋白(hFABP)基因位于染色体I上。它是心脏最丰富的蛋白质之一。hFABP结合两个脂肪酸分子并参与脂肪酰基辅酶A的运输,活跃于氧化过程,从而在线粒体中产生能量。目前,H-FABP的测定方法有酶联免疫法、放射免疫法与免疫层析等,但这些检测方法都存在一些缺陷,这些检测所存在的缺陷限制了它们的在临床诊断中的大规模应用,如检测过程中容易因溶液浓度与个体差异的情况造成检测干扰问题,抗干扰能力差,且试剂存放稳定性差,检测灵敏度不高,检测精确度与检测效果低下的缺点。
发明内容
本发明主要解决现有技术所存在的技术问题,从而提供一种能够有效增加检测稳定性与抗干扰能力,有效提高检测精确度与检测效果,提高了使用者大规模的进行检测应用的心型脂肪酸结合蛋白检测试剂盒。
为解决上述问题,本发明采用如下技术方案,包括试剂R1与试剂R2,所述R1试剂包括甘氨酸缓冲液100-300mmol/L,牛血清白蛋白3-8mmol/L,巯基乙醇30-50mmol/L,二硫苏糖醇60-80mmol/L,黄嘌呤氧化酶1.5-3.7KU/L,草氨酸钠10-20mmol/L,氯化钾8-15mmol/L;
所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球20-35mg/L,甘氨酸缓冲液40-60mmol/L,牛血清白蛋白2-6mmol/L,乙二胺四乙酸22-30mmol/L,甲基异噻唑啉酮15-28mmol/L,磷酸二氢钾12-16mmol/L。
作为优选,所述心型脂肪酸结合蛋白抗体的纳米微球的粒子直径为70-90nm。
作为优选,所述试剂R1与试剂R2的混合体积比为2:1,其中试剂R1中的甘氨酸缓冲液PH值在7.0-8.0,试剂R2中的甘氨酸缓冲液PH值在7.0-7.5。
作为优选,所述R1试剂包括甘氨酸缓冲液200mmol/L,牛血清白蛋白5mmol/L,巯基乙醇40mmol/L,二硫苏糖醇70mmol/L,黄嘌呤氧化酶2.8KU/L,草氨酸钠15mmol/L,氯化钾12mmol/L,所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球28mg/L,甘氨酸缓冲液50mmol/L,牛血清白蛋白4mmol/L,乙二胺四乙酸27mmol/L,甲基异噻唑啉酮22mmol/L,磷酸二氢钾14mmol/L。
本发明的有益效果是:该心型脂肪酸结合蛋白检测试剂盒能够有效增加检测稳定性与抗干扰能力,有效提高检测精确度与检测效果,提高了使用者大规模的进行检测应用。
具体实施方式
为了使本发明实现的技术手段、创作特征、达成目的与功效易于明白了解,下面结合具体实施例,进一步阐述本发明,但下述实施例仅仅为本发明的优选实施例,并非全部。基于实施方式中的实施例,本领域技术人员在没有做出创造性劳动的前提下所获得其它实施例,都属于本专利的保护范围。
一种心型脂肪酸结合蛋白检测试剂盒包括试剂R1与试剂R2,所述R1试剂包括甘氨酸缓冲液100-300mmol/L,牛血清白蛋白3-8mmol/L,巯基乙醇30-50mmol/L,二硫苏糖醇60-80mmol/L,黄嘌呤氧化酶1.5-3.7KU/L,草氨酸钠10-20mmol/L,氯化钾8-15mmol/L;所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球20-35mg/L,甘氨酸缓冲液40-60mmol/L,牛血清白蛋白2-6mmol/L,乙二胺四乙酸22-30mmol/L,甲基异噻唑啉酮15-28mmol/L,磷酸二氢钾12-16mmol/L。
所述心型脂肪酸结合蛋白抗体的纳米微球的粒子直径为70-90nm。
所述试剂R1与试剂R2的混合体积比为2:1,其中试剂R1中的甘氨酸缓冲液PH值在7.0-8.0,试剂R2中的甘氨酸缓冲液PH值在7.0-7.5。
作为优选,所述R1试剂包括甘氨酸缓冲液200mmol/L,牛血清白蛋白5mmol/L,巯基乙醇40mmol/L,二硫苏糖醇70mmol/L,黄嘌呤氧化酶2.8KU/L,草氨酸钠15mmol/L,氯化钾12mmol/L,所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球28mg/L,甘氨酸缓冲液50mmol/L,牛血清白蛋白4mmol/L,乙二胺四乙酸27mmol/L,甲基异噻唑啉酮22mmol/L,磷酸二氢钾14mmol/L。
本发明的有益效果是:该心型脂肪酸结合蛋白检测试剂盒能够有效增加检测稳定性与抗干扰能力,有效提高检测精确度与检测效果,提高了使用者大规模的进行检测应用。
以在所述,仅为本发明的具体实施方式,但本发明的保护范围并不局限于此,任何不经过创造性劳动想到的变化或替换,都应涵盖在本发明保护范围内。
Claims (4)
1.一种心型脂肪酸结合蛋白检测试剂盒,其特征在于:包括试剂R1与试剂R2,所述R1试剂包括甘氨酸缓冲液100-300mmol/L,牛血清白蛋白3-8mmol/L,巯基乙醇30-50mmol/L,二硫苏糖醇60-80mmol/L,黄嘌呤氧化酶1.5-3.7KU/L,草氨酸钠10-20mmol/L,氯化钾8-15mmol/L;
所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球20-35mg/L,甘氨酸缓冲液40-60mmol/L,牛血清白蛋白2-6mmol/L,乙二胺四乙酸22-30mmol/L,甲基异噻唑啉酮15-28mmol/L,磷酸二氢钾12-16mmol/L。
2.根据权利要求1所述的一种心型脂肪酸结合蛋白检测试剂盒,其特征在于:所述心型脂肪酸结合蛋白抗体的纳米微球的粒子直径为70-90nm。
3.根据权利要求1所述的一种心型脂肪酸结合蛋白检测试剂盒,其特征在于:所述试剂R1与试剂R2的混合体积比为2:1,其中试剂R1中的甘氨酸缓冲液PH值在7.0-8.0,试剂R2中的甘氨酸缓冲液PH值在7.0-7.5。
4.根据权利要求1所述的一种心型脂肪酸结合蛋白检测试剂盒,其特征在于:所述R1试剂包括甘氨酸缓冲液200mmol/L,牛血清白蛋白5mmol/L,巯基乙醇40mmol/L,二硫苏糖醇70mmol/L,黄嘌呤氧化酶2.8KU/L,草氨酸钠15mmol/L,氯化钾12mmol/L,所述试剂R2包括包被心型脂肪酸结合蛋白抗体的纳米微球28mg/L,甘氨酸缓冲液50mmol/L,牛血清白蛋白4mmol/L,乙二胺四乙酸27mmol/L,甲基异噻唑啉酮22mmol/L,磷酸二氢钾14mmol/L。
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