EZElisa™ Non Metastatic Cells
1,Protein NM 23A Expressed In（NME 1）ELISA试剂盒-EZElisa™ Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit- 询价
- Biogradetech
- 美国
- A-QEK13237-96wells
- 2025年07月10日
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- 文献和实验
- 技术资料
- 保存条件：
运输过程中保存：2-8℃
- 保质期：
1年
- 英文名：
EZElisa™ Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit
- 库存：
100
- 供应商：
艾美捷科技
EZElisa™ Non Metastatic Cells 1,Protein NM 23A Expressed In（NME 1）ELISA试剂盒，EZElisa™ Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit， Non Metastatic Cells 1,Protein NM 23A Expressed In（NME 1）ELISA试剂盒, Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit
产品名称：EZElisa™ Nod Like Receptor Pyrins-4（Rat NLRP 4）ELISA试剂盒-EZElisa™ Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit
产品货号：A-QEK13237-96wells
产品规格：96wells
Enzyme Immunoassay for the estimation of Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA in serum and plasma, tissue homogenates and other biological fluids.
Availability: 3 - 4 Weeks | Pack Size: 1 x 96 wells
种属：Rat
检测方法：比色法
检测范围：0.312-20ng/mL
该EZElisa™ Non Metastatic Cells 1，Protein NM 23A Expressed In（NME 1）ELISA KitELISA的特点包括：即用即用的操作步骤标准化和高重复性批次之间的一致性准确性和精确性经过七个点的验证，符合金环标准质量ELISA的要求，这是Biogradetech质量的基准标志。EZElisa™ ELISA试剂盒用于评估样品中的特定生物标志物，样品可以是血清
运输过程中保存：2-8℃
点击：EZElisa™ Nod Like Receptor Pyrins-4（Rat NLRP 4）ELISA试剂盒-EZElisa™ Non Metastatic Cells 1, Protein NM23A Expressed In (NME1) ELISA Kit更多Biogradetech产品信息价格，货期，产品说明，百度搜“艾美捷科技”进入官网网站，查看具体产品且快速下单。
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文献和实验a method allowing RNA visualization in live cells. The method is based on fluorescent protein complementation regulated by RNA?aptamer/RNA?binding protein interactions. Based on these two principles, a fluorescent ribonucleoprotein complex is assembled
#1). Figure 2. Silencer ™ siRNA Validation Data Generated Using Applied Biosystems TaqMan® Gene Expression Assays. The indicated Silencer Validated siRNAs were transfected into HeLa Cells at 30 nM. RNA was isolated 48 hours later and analyzed by one-step
. As negative control the reaction was also carried out using a non transfected CHO lysate sample. The rate of phenol formation was followed over 2 minute period/270nm/25°C. The activity is expressed in U/L Immuno-reactivity of paraoxonase-1
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