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resDetect™ Human TPO ELISA Kit (Residue Testing)

For research use only.

产品参数(Product Specifications)

Assay TypeSandwich-ELISA
AnalyteTPO
Format96T(8×12 strips)
ReactivityHuman
Regulatory StatusRUO
Sensitivity<12.5 pg/mL
Standard Curve Range12.5 pg/mL-400 pg/mL
Assay Time3 hr 20 min
Suitable Sample TypeFor the detection and quantitative determination of TPO in human serum and cell culture supernates.
Sample volume100 uL

产品概述(Product Overview)

resDetect™ Human TPO ELISA Kit (Residue Testing) is based on the ELISA sandwich method and is used to detect and quantitatively determine GMP Human TPO residues in cell culture supernatants, serum, and plasma. The kit contains GMP human TPO (ACROBiosystems, cat# GMP-THNH25) to ensure accurate assay results and is designed to provide a reliable solution for CAR-T product quality assessment during drug development and CMC quality control stages. It can also be used as a universal detection tool for the quantitative determination of Human TPO.

重构方法(Reconstitution)

Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.

存储(Storage)

1. Unopened kit should be stored at 2℃-8℃ upon receiving.

2. Find the expiration date on the outside packaging and do not use reagents past their expiration date.

3. The opened kit should be stored per components table. The shelf life is 30 days from the date of opening.

组分(Materials Provided)

IDComponentsSize
RES034-C01Pre-coated Anti-TPO Antibody Microplate1 plate(8×12 strips)
RES034-C02Human TPO Standard20 μg
RES034-C03Biotin-Anti-TPO Antibody20 μg
RES034-C04Streptavidin-HRP50 μL
RES034-C0510×Washing Buffer50 mL
RES034-C062×Dilution Buffer50 mL
RES034-C07Substrate Solution12 mL
RES034-C08Stop Solution7 mL

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
 

典型数据-Typical Data Please refer to DS document for the assay protocol.

TPO TYPICAL DATA

For each experiment, a standard curve needs to be set for each micro-plate, and the specific OD value may vary depending on different laboratories, testers, or equipments. The following example data is for reference only.

 

验证(Validation)

稀释线性(Dilution Linearity)

To assess the linearity of the assay, samples spiked with high concentrations of TPO were serially diluted with calibrator diluent to produce samples with values within the dynamic range of the assay.

TPO DILUTION LINEARITY

批内差异(Intra-Assay Statistics)

Three samples of known concentration were tested ten times on one plate to assess intra-assay precision.

TPO INTRA-ASSAY STATISTICS

批间差异(Inter-Assay Statistics)

Three samples of known concentration were tested in three separate assays to assess inter-assay precision.

TPO INTER-ASSAY STATISTICS

回收率(Recovery)

Five parts of blank T cell culture supernatant were added with different concentrations of human TPO, and the T cell culture supernatant without human TPO was used as background to calculate the recovery rate. The range of the recovery rate is 94.7-108.9%, and the average recovery is 102.1%.

TPO RECOVERY

 
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背景(Background):TPO

Thrombopoietin (TPO) is a 332 amino acid glycoprotein made primarily in the liver and act as the major physiological regulator of platelet production. TPO binds the TPO receptor, activates JAK and STAT pathways, thus stimulating megakaryocyte growth and platelet production. Additionally, further investigation uncovered that thrombopoietin is a critical cytokine promoting hematopoietic rebound after myeloablation and its transcripts are expressed by multiple cellular sources.

 

前沿进展

Comparative Evaluation of Water Soluble Photoinitiators on the Mechanical and Physical Properties of Experimental Composite: An In Vitro Study
Tulasi, Sihivahanan, Venkatesh
Indian J Dent Res (2024) 35 (4), 454-458
Abstract: Composite resin restoration is technique sensitive, where there is poor control over moisture leading to incomplete polymerization of the monomers. Hence, it is imperative to study a material which improves the mechanical and physical properties of the resin composite in the moist, oral environment, which is less affected by the saliva.The aim of this study was to synthesize composite resin by combining water soluble photoinitiator such as 2,4,6-trimethylbenzoyl phosphine oxide (TPO) (type II) and camphorquinone (CQ) photoinitiator (type I) and to investigate mechanical and physical properties with and without salivary contamination when compared to traditional composite with CQ alone.Experimental composite resin was synthesized by combining water soluble photoinitiator such as 2,4,6-trimethylbenzoyl phosphine oxide (TPO) with CQ photoinitiator. Samples were prepared based on ISO 4049 guidelines and divided into experimental composite with salivary contamination (n = 50), and without salivary contamination (n = 50) and traditional composite (SOLARE X-GC company) with salivary contamination (n = 50) and without salivary contamination (n = 50). Properties such as compressive strength, tensile strength, shear bond strength, degree of conversion, and depth of cure were evaluated.Experimental composite with salivary contamination had shown statistically significant difference in mechanical and physical properties when compared to traditional composite.This study concluded that combining water soluble photoinitiator such as TPO (type II) with CQ (type I) provides a synergistic effect by increasing the mechanical properties under salivary conditions.Copyright © 2025 Indian Journal of Dental Research.
Maternal thyroid dysfunction and depressive symptoms during pregnancy and child behavioral and emotional problems - an ECHO multi-cohort investigation
Moog, Mansolf, Sherlock et al
J Affect Disord (2025)
Abstract: Maternal thyroid dysfunction and maternal depression during pregnancy may increase the risk of child behavioral and emotional problems. We sought to investigate the independent and interactive associations of these two risk factors with child behavior problems.We combined data from four cohorts in the Environmental influences on Child Health Outcomes (ECHO) program (N = 949). Maternal thyroid function (thyroid-stimulating hormone [TSH], free thyroxine [fT4], thyroid peroxidase autoantibodies [TPO-Ab], fT4/TSH ratio) was measured predominantly during the first half of pregnancy. We harmonized maternal depression into a continuous measure of antepartum depressive symptomatology and a dichotomous measure reflecting (history of) clinical depression. Child internalizing and externalizing problems were harmonized to the T-score metric of the Child Behavior Checklist. We used multiple linear regression and random effects meta-analysis to assess the average relationship between each predictor and outcome, and the variability in these relationships across cohorts.Across cohorts, antepartum depressive symptomatology was positively associated with both internalizing (meta B = 2.879, 95 % CI 1.87-3.89, p < .001) and externalizing problems (meta B = 1.683, 95 % CI 0.67-2.69, p = .001). None of the indicators of maternal thyroid function was associated with child behavior problems across cohorts. TPO-Ab concentrations were positively associated with child externalizing problems only in offspring of depressed mothers (meta B = 3.063, 95 % CI 0.73-5.40, p = .010).This study supports the importance of maternal antepartum mental health for child behavior across diverse populations. However, we found little empirical evidence for an association between maternal thyroid function within the normal range during pregnancy and child behavioral problems.Copyright © 2025. Published by Elsevier B.V.
The Human Thyroid-Derived CI-huThyrEC Cell Line Expresses the Thyrotropin (TSH) Receptor and Thyroglobulin but Lacks Other Essential Characteristics of Thyroid Follicular Cells
Halbout, Kopp
Biomolecules (2025) 15 (3)
Abstract: Background: Thyroid hormone synthesis requires the normal function of thyroid follicular cells and adequate nutritional intake of iodine. For in vitro studies on thyroid cell pathophysiology, the immortalized FRTL5 rat thyroid cell line and a derivative thereof, the PCCL3 cell line, are widely used. However, a permanent human thyroid cell line is currently lacking. A recent report described a cell line obtained from human thyroid cells designated as Cl-huThyrEC. Methods: Four clones of Cl-huThyrEC cells were obtained and cultured in the presence of thyroid stimulating hormone (TSH). The expression of key genes defining the thyroid follicular cell phenotype was determined by reverse-transcription PCR (RT-PCR) in FRTL5, PCCL3, and Cl-huThyrEC cells. The latter were cultured as monolayers and as organoids in Matrigel. Iodide uptake was measured and compared among the cell lines. Results: Gene expression analysis reveals that Cl-huThyrEC cells express the thyroid-restricted transcription factors (PAX8, NKX2.1, FOXE1), the TSH receptor (TSHR), and thyroglobulin (TG), but they do not express the sodium-iodide symporter (NIS), thyroid peroxidase (TPO), and pendrin (SLC26A4). In functional studies, Cl-huThyrEC cells are unable to concentrate iodide. Conclusions: Despite the expression of certain key genes that are limited or restricted to thyroid follicular cells, Cl-huThyrEC cells lack some of the essential characteristics of thyroid follicular cells, in particular, NIS. Hence, their utility as a model system for thyroid follicular cells is limited.
Hashimoto's Encephalopathy: Clinical Features, Therapeutic Strategies, and Rehabilitation Approaches
Manocchio, Magro, Massaro et al
Biomedicines (2025) 13 (3)
Abstract: Hashimoto's encephalopathy (HE), also known as steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT), is an autoimmune disorder with heterogeneous presentation that poses diagnostic challenges. This review synthesizes the current literature to clarify the clinical, laboratory, and radiological features of SREAT/HE, including the diagnostic utility of thyroid peroxidase (TPO) antibodies, cerebrospinal fluid (CSF) abnormalities, and neuroimaging findings. Cognitive impairment and behavioral changes are common in HE, but specific manifestations vary widely, which can lead to misdiagnosis. While elevated TPO antibodies are frequently observed, a direct causal relationship with HE is unlikely, and their presence may indicate a general state of autoimmunity. Corticosteroids remain the cornerstone of treatment, although responses vary, and alternative immunosuppressive agents or intravenous immunoglobulin may be needed in some cases. Evidence regarding rehabilitation for people affected by HE is limited, but neurorehabilitation strategies adapted from other neurological conditions, including cognitive re-education (CR), physical therapy, and psychosocial support, may be beneficial. Further research is needed to elucidate the underlying mechanisms of SREAT, refine the diagnostic criteria, and develop more targeted and effective therapies, including rehabilitation strategies, for this debilitating neurological disorder.
Showing 1-4 of 7455 papers.
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