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 >  Protein>NSE >NSE-M5147

Mouse NSE Protein, His Tag (MALS verified)

分子别名(Synonym)

Neuron-specific enolase,gamma-enolase

表达区间及表达系统(Source)

Mouse NSE, His Tag (NSE-M5147) is expressed from E. coli cells. It contains AA Met 1 - Met 431 (Accession # Q545V3-1).

Predicted N-terminus: Met

Request for sequence

蛋白结构(Molecular Characterization)

NSE Structure

This protein carries a polyhistidine tag at the N-terminus

The protein has a calculated MW of 49.3 kDa. The protein migrates as 47-50 kDa under reducing (R) condition (SDS-PAGE).

内毒素(Endotoxin)

Less than 1.0 EU per μg by the LAL method.

纯度(Purity)

>95% as determined by SDS-PAGE.

>95% as determined by SEC-MALS.

制剂(Formulation)

Lyophilized from 0.22 μm filtered solution in 20 mM Tris, 0.5 M Arginine, pH7.5 with trehalose as protectant.

Contact us for customized product form or formulation.

重构方法(Reconstitution)

Please see Certificate of Analysis for specific instructions.

For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.

存储(Storage)

For long term storage, the product should be stored at lyophilized state at -20°C or lower.

Please avoid repeated freeze-thaw cycles.

This product is stable after storage at:

  1. -20°C to -70°C for 12 months in lyophilized state;
  2. -70°C for 3 months under sterile conditions after reconstitution.

质量管理控制体系(QMS)

  1. 质量管理体系(ISO, GMP)
  2. 质量优势
  3. 质控流程
 

电泳(SDS-PAGE)

NSE SDS-PAGE

Mouse NSE, His Tag on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%.

SEC-MALS

NSE SEC-MALS

The purity of Mouse NSE, His Tag (Cat. No. NSE-M5147) is more than 95% and the molecular weight of this protein is around 100-115 kDa verified by SEC-MALS.

Report

 

活性(Bioactivity)-ELISA

NSE ELISA

Immobilized Mouse NSE, His Tag (Cat. No. NSE-M5147) at 1 μg/mL (100 μL/well) can bind Anti-NSE Antibody with a linear range of 0.004-0.125 μg/mL (QC tested).

Protocol

 
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背景(Background)

Neuron-specific enolase (NSE) is known to be a cell specific isoenzyme of the glycolytic enzyme enolase. It is also known as
gamma-enolase or nolase 2 (ENO2). It has neurotrophic and neuroprotective properties on a broad spectrum of central nervous system (CNS) neurons. NSE is a highly specific marker for neurons and peripheral neuroendocrine cells. In clinical, NSE could be used as a biomarker for neuronal injury.

 

前沿进展

The Association Study Between Cytokines and the Risk for Cerebral Palsy
Wang, Wang, Yang et al
Mediators Inflamm (2025) 2025, 3742331
Abstract: Background: Cerebral palsy (CP) is a debilitating condition characterized by abnormal movement or posture beginning early in development. Recent evidence has shown that immunological abnormalities are associated with an increased risk of CP. However, there are no valuable biomarkers for CP diagnosis. Methods: In this case-control study, we recruited 108 children with CP and 52 healthy children as controls. The white blood cell (WBC) counts and the levels of inflammatory markers (interleukin-1β (IL-1β), sIL-2R, interleukin-6 (IL-6), IL-8, IL-10, and tumor necrosis factor-α (TNF-α)), neuron-specific enolase (NSE), immunoglobulin E (IgE), and C3/C4 in the blood were measured and the results were statistically analyzed. Subgroup analyzes based on age, complications, and clinical subtypes were also carried out. Results: Compared with the controls, CP patients had elevated levels of NSE, sIL-2R, and TNF-α. There were no differences in WBC count, IL-1β, IL-6, IL-8, IL-10, IgE, C3, or C4. Subgroup analysis revealed significant differences in the personal-social developmental quotient (DQ) among the different CP subtypes. We found that TNF-α, sIL-2R, gross motor DQ, and adaptive DQ were greater in children with CP without epilepsy (EP) than in those with EP. Correlation analysis revealed positive correlations between TNF-α and sIL-2R, gross motor DQ, fine motor DQ, adaptive DQ, and personal-social DQ; moreover, sIL-2R was positively correlated with TNF-α, gross motor DQ, adaptive DQ, personal-social DQ, and eosinophil (EO) count and negatively correlated with age. NSE and TNF-α were associated with a 1.64-fold and 1.66-fold increased risk of CP, respectively. The peripheral blood NSE and TNF-α levels exhibited good diagnostic value for CP. Moreover, receiver operating characteristic (ROC) curve analysis revealed a significant increase in the area under the curve (AUC) when these indicators were combined. Conclusions: This study revealed significant associations between NSE and TNF-α and CP risk, suggesting that NSE and TNF-α might be useful blood biomarkers for identifying patients at high risk of CP.Copyright © 2025 Baotian Wang et al. Mediators of Inflammation published by John Wiley & Sons Ltd.
Status epilepticus in the neonate
Nagarajan, Ghosh
BMJ Paediatr Open (2025) 9 (1)
Abstract: Status epilepticus in the neonate (NSE) is a medical emergency that often results in dire consequences. Minimising injury from NSE is essential. The diagnosis of NSE can be challenging as neonates frequently have electrographic only seizures and an EEG is essential for recognition of seizures and seizure burden. The lack of a universally accepted definition of NSE, possible adverse effects from commonly used antiseizure medications, debate regarding the best treatment packages for NSE, limited access to EEG and investigations for aetiology of NSE add to the clinical conundrum. In this review, we aim to present what is known, highlight the importance of EEG monitoring for diagnosis and treatment, discuss what is not known and suggest a practical paradigm for the management of NSE.© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.
Immunohistochemical and histomorphologic characterization of canine neoplasms of the disseminated neuroendocrine system
Champion, Miller, Parry et al
Vet Pathol (2025)
Abstract: Canine neoplasms of the diffuse neuroendocrine system are an enigmatic and heterogeneous group of neoplasms with a wide spectrum of immunohistochemical properties and morphologic features. Through the utilization of tissue microarrays, 82 canine neoplasms of the disseminated neuroendocrine system from 16 different anatomic locations were evaluated. The prototypical canine neoplasm of the disseminated neuroendocrine system was composed of rounded polygonal neoplastic cells arranged in packets supported by delicate fibrovascular stroma. Neoplastic cells typically had moderate quantities of pale eosinophilic cytoplasm stippled by numerous fine argyrophilic granules, round nuclei with finely stippled chromatin, and inconspicuous nucleoli. Immunohistochemical assays utilized in this study included chromogranin A, neuron-specific enolase (NSE), microtubule-associated protein 2 (MAP2), pan-cytokeratin, oligodendrocyte transcription factor 2 (OLIG2), protein gene product 9.5 (PGP9.5), vimentin, synaptophysin, neuronal nuclei (NeuN), S100, SRY-related HMG-box 10 (SOX10), glial fibrillary acidic protein (GFAP), insulinoma-associated protein 1 (INSM1), CD56, and antigen Kiel 67 (Ki67). The 4 immunohistochemical assays that were positive in over 50% of cases included PGP9.5 (77/82, 94%), NSE (68/82, 83%), synaptophysin (59/82, 72%), and chromogranin A (56/82, 69%). In 81/82 (99%) cases, neoplastic cells immunolabeled with at least 1 of these 4 assays, and thus, these 4 immunohistochemical assays are deemed most useful when attempting to substantiate that a neoplasm is of neuroendocrine origin.
Assessment and estimation of runoff and soil loss using novel machine learning techniques for conservation bench terraces
Kumar, Kumar, Sharma et al
Sci Total Environ (2025) 973, 179093
Abstract: Conservation of land and water resources, especially in terms of runoff and soil loss, has the utmost priority in enhancing agricultural production, especially in the foothills of the Himalayas. Many engineering measures have been applied to reduce runoff velocity and soil loss. The present study deals with the effectiveness of Conservation Bench Terraces (CBT) as engineering measures constructed in the outer foothills of the Himalayas (ICAR-IISWC, Dehradun, India) to reduce runoff and soil losses in the context of strom size. Further, the development of runoff and soil loss models using available climatic parameters and machine learning techniques. The parameters used were maximum temperature (Tmax, °C), minimum temperature (Tmin, °C), soil temperature (Tsoil, °C), rainfall (mm), pan evaporation (mm), runoff (mm), and soil loss (Mg/ha) during the year 2007-2015. The machine learning techniques, artificial neural network (ANN), linear function support vector machine (SVM-L), radial function support vector machine (SVM-R), multiple linear regression (MLR) along with hybridization of ANN and both function of SVM with wavelet transform as WANN, WSVM-L and WSVM-R, respectively were employed for the estimation of runoff and soil loss. Their performance evaluation was also assessed with the well accepted quantitative and qualitative indicators. The results revealed that the CBT has reduced runoff and soil losses from the experimental plots. The estimation of runoff and sediment were best predicted by SVM-L model with PCC, RMSE, NSE, MAE, and WI values as 0.82 and 0.56, 18.21 and 0.11, 0.41 and 0.16, 13.45 and 0.069, 0.799 and 0.716, respectively for runoff and sediment modelling. The wavelet hybridized models were inaccurate in prediction in this case. Furthermore, sensitivity analysis were carried out and found rainfall was the most sensitive parameter. The SVM-L model could be applied for the estimation of runoff and soil loss from given parameters, which is helpful in planning and designing of CBTs in larger areas. The results indicate CBT's effectiveness in reducing plot-level runoff and soil losses is comparitively high, specially for storm size lesser than 75 mm. The SVM-L model can act as a powerful tool for policymakers and implementing agencies in planning and designing of CBTs.Copyright © 2025 Elsevier B.V. All rights reserved.
Showing 1-4 of 8293 papers.
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NSE靶点信息
英文全称:Gamma-enolase
中文全称:γ-烯醇化酶
种类:
上市药物数量:0详情
临床药物数量:0详情
最高研发阶段:临床前
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