EZElisa™抗甲状腺过氧化物酶抗体（大鼠TPO-Ab）E
LISA试剂盒-EZElisa™ anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) ELISA Kit- 询价
- Biogradetech
- 美国
- A-QEK13573-96wells
- 2025年07月09日
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- 详细信息
- 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™ anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) ELISA Kit
- 库存：
100
- 供应商：
艾美捷科技
EZElisa™抗甲状腺过氧化物酶抗体（大鼠TPO-Ab）ELISA试剂盒，EZElisa™ anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) ELISA Kit，抗甲状腺过氧化物酶抗体（TPO-Ab）ELISA试剂盒, anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) ELISA Kit
产品名称：EZElisa™细胞肿瘤抗原p53（大鼠Tp53）ELISA试剂盒-EZElisa™ anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) ELISA Kit
产品货号：A-QEK13573-96wells
产品规格：96wells
Enzyme Immunoassay for the estimation of anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) 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：0.781-50IU/ml
该EZElisa™抗甲状腺过氧化物酶抗体（大鼠TPO-Ab）ELISA试剂盒ELISA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™细胞肿瘤抗原p53（大鼠Tp53）ELISA试剂盒-EZElisa™ anti-Thyroid-Peroxidase Antibody (Rat TPO-Ab) 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ELISA Procedure for Measuring Serum Antibody Titer
of an antibody is shown in Figure 22. The titer was estimated to be 1 in 2400. Figure 22. Antibody titer graph (X = dilution corresponding to Ab titer) Further Methods for Evaluating Anti-peptide Antibodies If the antibodies are to be used as a reagent
Whole mount antibody staining of zebrafish embryos for markers of segmentation
4. Wash for a minimum of 2 hours with several changes of 0.2% saponin in PBS (can store in cold room at this point). 5. Incubate overnight with 0.5 ml secondary antibodyconjugated to peroxidase (HRP) (Goat anti- mouse IgG+IgM-HRP) @ 1/500at 4oC.
Antibody Production: Activity-Dependent Neuroprotective Protein (ADNP) as an Example
by a secondary antibody horseradish peroxidase conjugated anti-rabbit IgG prepared in goat and developed with ECL. All antibodies recognized intact ADNP in both cytoplasmic and nuclear fractions. This work developed antibodies against ADNP and NAP
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