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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 Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) ELISA Kit
| Product name: | Human Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) ELISA Kit |
| Method: | sandwich |
| Synonyms: | Carboxypeptidase M |
| Catalog number: | DL-UCHL1-Hu |
| Detection range: | 78-5,000pg/mL |
| Size: | 96T |
| Assay length | 1-4.5Hours |
| Price: | inquiry |
| Quality guarantee period: | for 12 months |
Human Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) ELISA Kit
Introduction
| 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 |
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 |
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-NMB-Mu 小鼠神经介素B(NMB) ELISA Kit mouse Neuromedin B (NMB) ELISA Kit Mus musculus mouse 12.35-1000pg/mL 4.75pg/mL 96T 3620 12 months
DL-CRP-Ra 大鼠C反应蛋白(CRP) ELISA Kit Rat C Reactive Protein (CRP) ELISA Kit Rattus norvegicus Rat 0.781-50ng/mL 0.35ng/mL 96T 3040 12 months
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DL-PPARg-Ra 大鼠过氧化物酶体增殖物激活受体γ(PPARγ) ELISA Kit Rat Peroxisome Proliferator Activated Receptor Gamma (PPARg) ELISA Kit Rattus norvegicus Rat 0.156-10ng/mL 0.058ng/mL 96T 3800 12 months
DL-PPARg-Mu 小鼠过氧化物酶体增殖物激活受体γ(PPARγ) ELISA Kit mouse Peroxisome Proliferator Activated Receptor Gamma (PPARg) ELISA Kit Mus musculus mouse 0.156-10ng/mL 0.066ng/mL 96T 3620 12 months
DL-F2-Hu 人凝血因子Ⅱ(F2) ELISA Kit human Coagulation Factor II (F2) ELISA Kit Homo sapiens human 9.375-600ng/mL 0.3ng/mL 96T 3530 12 months
DL-IFNa-Mu 小鼠干扰素α(IFNα) ELISA Kit mouse Interferon Alpha (IFNa) ELISA Kit Mus musculus mouse 15.625-1000pg/mL 6.3pg/mL 96T 2900 12 months
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文献和实验spermatogonia coexpress GPR125, integrin, alpha 6 (ITGA6), THY1 (also known as CD90), GFRA1, and ubiquitin carboxyl-terminal esterase L1 (UCHL1), markers for rodent or pig SSCs/progenitors, suggesting that GPR125- and GFRA1-positive spermatogonia
(Ubiquitin C-terminal hydrolase-L1,UCH-L1)是一种主要分布于脑内,同时对人类大脑具有高度特异性的球蛋白。 癫痫大发作组脑脊液 UCH-L1 水平显著高于部分性发作组和对照组。癫痫患者的脑脊液 UCHL1 水平与癫痫发作的严重程度和癫痫发作的持续时间密切相关。癫痫发作后 6h 内检验患者血清 UCH-L1 及 S100β 水平,结果显示癫痫组 UCHL-1 及 S100β 水平显著高于精神源性非癫痫性发作组及健康人群组,精神源性非癫痫性发作组 S100β 水平显著高于健康对照
secondary antibody review -- data from 99 publications
cytometry used as a control to detect cell responses targeted antigen 7 Alexa Fluor 488 7 Cy3 8 goat IgG Alexa Fluor 488 1:2000 detect antibody binding in human embryonic kidney 293T cells Invitrogen 9 donkey
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