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- 详细信息
- 文献和实验
- 技术资料
- 库存:
大量供应
- 供应商:
康朗生物
- 检测范围:
详见说明书
- 检测方法:
夹心法
- 应用:
ELISA 定量检测
- 标记物:
详见说明书
- 样本:
血清,血浆,尿液 细胞裂解液,组织匀浆,细胞培养上清液
- 规格:
96T/盒
Human Prohibitin (PHB) ELISA Kit
| Product name: | Human Prohibitin (PHB) ELISA Kit |
| Method: | sandwich |
| Synonyms: | B4 integrin interactor,CAB,EIF3A,eIF-6,ITGB4BP |
| Catalog number: | DL-PHB-Hu |
| Detection range: | 0.312-20ng/mL |
| Size: | 96T |
| Assay length | 1-4.5Hours |
| Price: | inquiry |
| Quality guarantee period: | for 12 months |
Introduction
Human Prohibitin (PHB) ELISA Kit
| Item | Standard | Test Result | |
| Description | This immunoassay kit allows for the specific measurement of this index in serum, Plasma , Urine ,tissue homogenates and Cell culture supernates and Other biological fluids.. |
Conform | |
| Identification | Colorimetric | Positive | |
| Composition | Pre-coated, ready to use 96-well strip plate Standard (freeze dried) Standard Diluent Detection Reagent A Detection Reagent B Assay Diluent A Assay Diluent B TMB Substhumane Stop Solution Wash Buffer(30 x concenthumane) Plate sealer for 96 wells Instruction manual |
1 2 1 × 20ml 1× 120μl 1× 120μl 1 × 12ml 1 × 12ml 1 × 9ml 1 ×6ml 1 ×20ml 2 1 |
Conform |
Human Prohibitin (PHB) ELISA Kit
Test principle
The microtiter plate provided in this kit has been pre-coated with an antibody specific to this index. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for this index and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain the index, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of the index in the samples is then determined by comparing the O.D. of the samples to the standard curve
Recovery
Matrices listed below were spiked with certain level of recombinant the index and the recovery humanes were calculated by comparing the measured value to the expected amount of the index in samples.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 81-93 | 86 |
| EDTA plasma(n=5) | 80-97 | 88 |
| heparin plasma(n=5) | 90-101 | 95 |
Human Prohibitin (PHB) ELISA Kit
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concenthumanion of the index and their serial dilutions. The results were demonsthumaned by the percentage of calculated concenthumanion to the expected.
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 82-96% | 83-98% | 81-99% | 93-101% |
| EDTA plasma(n=5) | 88-101% | 86-95% | 90-102% | 80-93% |
| heparin plasma(n=5) | 80-91% | 82-90% | 95-104% | 79-95% |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level the index were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level the index were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Stability
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end
Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37℃;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37℃;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37℃;
7. Add 50µL Stop Solution. Read at 450 nm immediately.
DL-KLF4-Hu 人Kruppel样因子4(KLF4) ELISA Kit human Kruppel Like Factor 4, Gut (KLF4) ELISA Kit Homo sapiens human 0.156-10ng/mL 0.060ng/mL 96T 3705 12 months
DL-ABCA1-Hu 人ATP结合盒转运蛋白A1(ABCA1) ELISA Kit human ATP Binding Cassette Transporter A1 (ABCA1) ELISA Kit Homo sapiens human 0.156-10ng/mL 0.053ng/mL 96T 3705 12 months
DL-KP-Hu 人利钾尿肽(KP) ELISA Kit human Kaliuretic Peptide (KP) ELISA Kit Homo sapiens human 123.46-10000 pg/mL 39.8 pg/mL 96T 3705 12 months
DL-FABP3-Hu 人心型脂肪酸结合蛋白(FABP3) ELISA Kit human Fatty Acid Binding Protein 3, Muscle And Heart (FABP3) ELISA Kit Homo sapiens human 0.625-40ng/mL 0.215ng/mL 96T 3705 12 months
DL-TIEG1-Hu 人TGFβ诱导早期应答基因1(TIEG1) ELISA Kit human TGF Beta Inducible Early Response Gene 1 (TIEG1) ELISA Kit Homo sapiens human 0.313-20ng/mL 0.122ng/mL 96T 3530 12 months
DL-TECK-Hu 人胸腺表达趋化因子(TECK) ELISA Kit human Thymus Expressed Chemokine (TECK) ELISA Kit Homo sapiens human 31.25-2000pg/mL 11.5pg/mL 96T 3705 12 months
DL-AR-Hu 人雄激素受体(AR) ELISA Kit human Androgen Receptor (AR) ELISA Kit Homo sapiens human 0.313-20ng/mL 0.115ng/mL 96T 3705 12 months
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文献和实验外膜上,而后与LC3II结合介导线粒体自噬。来自武汉大学生命科学学院宋质银教授研究组发表了题为“PHB2 (prohibitin 2) promotes PINK1-PRKN/Parkin-dependent mitophagy by the PARL-PGAM5-PINK1 axis (PHB2通过PRAL-PGAM5-PINK1轴线促进PINK1-Parkin介导的线粒体自噬)”的最新研究成果,揭示了PHB2调节线粒体自噬的新的分子机制,而且发现了以PHB2为靶点通过阻止线粒体自噬来抑制肿瘤细胞的生存可作
有替代前者的趋势。由于ABS-ELISA较普通ELISA多用了两种试剂,增加了操作步骤,在临床检验中ABS-ELISA应用不多。科研项目中检测微量的成分如细胞因子常采用本法。晶美分装ELISA KIT采用的方法:1, TORCH及传染病试剂盒(间接法),见2.2.32, TORCH-IgM捕获法特色:包被抗体,标记抗原原理:3, 细胞因子试剂盒采用的方法路线(ABC-ELISA)原理产品特色:采用ABC法,灵敏度更高,特异性更强。生物素抗体和酶联物是浓缩的,使用前需用相应的缓冲液稀释。酶联物可以通用
的原理用于分子诊断方面:TrimGen公司的KRAS Mutation Detection Kit在96孔板里一次能实现7/8个KRAS突变位点的检测。 另外基于相同原理的技术还有PPT-ELISA。这是用来筛截短突变的,相关文章见:1,Rapid screen for truncating ATM mutations by PTT-ELISA . 2,An ELISA-based high throughput protein truncation test
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