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Human TSLP R Protein, Fc Tag (MALS verified)

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分子别名(Synonym)

TSLP R,CRLF2,IL-XR,ILXR,p2RY8,CRLF2 fusion,TSLP receptor,TSLPR,CRL2,CRLF2Y,Cytokine receptor-like 2

表达区间及表达系统(Source)

Human TSLP R, Fc Tag (TSR-H525a) is expressed from human 293 cells (HEK293). It contains AA Gly 25 - Lys 231 (Accession # Q9HC73-1).

Predicted N-terminus: Gly 25

Request for sequence

蛋白结构(Molecular Characterization)

TSLP R Structure

This protein carries a human IgG1 Fc tag at the C-terminus.

The protein has a calculated MW of 50.4 kDa. The protein migrates as 60-65 kDa when calibrated against Star Ribbon Pre-stained Protein Marker under reducing (R) condition (SDS-PAGE) due to glycosylation.

内毒素(Endotoxin)

Less than 1.0 EU per μg by the LAL method.

纯度(Purity)

>95% as determined by SDS-PAGE.

>90% as determined by SEC-MALS.

制剂(Formulation)

Lyophilized from 0.22 μm filtered solution in Tris with Glycine, Arginine and NaCl, 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)

TSLP R SDS-PAGE

Human TSLP R, Fc Tag on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95% (With Star Ribbon Pre-stained Protein Marker).

SEC-MALS

TSLP R SEC-MALS

The purity of Human TSLP R, Fc Tag (Cat. No. TSR-H525a) is more than 90% and the molecular weight of this protein is around 115-140 kDa verified by SEC-MALS.

Report

 

活性(Bioactivity)-ELISA

TSLP R ELISA

Immobilized Human TSLP R, Fc Tag (Cat. No. TSR-H525a) at 5 μg/mL (100 μL/well) can bind Biotinylated Human TSLP, His,Avitag (Cat. No. TSP-H82Eb) with a linear range of 4-31 ng/mL (QC tested).

Protocol

TSLP R ELISA

Biotinylated Human TSLP (R127A, R130A), His,Avitag (Cat. No. TSP-H82E0) immobilized at 2 μg/mL (100 μL/well) via precoated 5 μg/mL (100 μL/well) of Human TSLP R, Fc Tag (Cat. No. TSR-H525a), can bind can bind Human IL-7 R alpha, Mouse IgG2a Fc Tag (Cat. No. IL7-H5258) with a linear range of 1-39 ng/mL (Routinely tested).

Protocol

 

活性(Bioactivity)-SPR

TSLP R SPR

Captured Human TSLP Protein, His Tag, premium grade (Cat. No. TSP-H52Hb) on CM5 Chip via anti-His antibody, can bind Human TSLP R, Fc Tag (Cat. No. TSR-H525a) with an affinity constant of 1.81 nM as determined in SPR assay (Biacore T200) (Routinely tested).

Protocol

TSLP R SPR

Captured Human TSLP (R127A, R130A), His Tag (Cat. No. TSP-H52Ha) on CM5 Chip via anti-His antibody, can bind Human TSLP R, Fc Tag (Cat. No. TSR-H525a) with an affinity constant of 4.22 nM as determined in SPR assay (Biacore T200) (Routinely tested).

Protocol

 

活性(Bioactivity)-BLI

TSLP R BLI

Loaded Human TSLP R, Fc Tag (Cat. No. TSR-H525a) on Protein A Biosensor, can bind Human TSLP (R127A, R130A), His Tag (Cat. No. TSP-H52Ha) with an affinity constant of 16 nM as determined in BLI assay (ForteBio Octet Red96e) (Routinely tested).

Protocol

TSLP R BLI

Loaded Human TSLP R, Fc Tag (Cat. No. TSR-H525a) on Protein A Biosensor, can bind Human TSLP Protein, His Tag, premium grade (Cat. No. TSP-H52Hb) with an affinity constant of 24.7 nM as determined in BLI assay (ForteBio Octet R8) (Routinely tested).

Protocol

TSLP R BLI

Loaded Human TSLP R, Fc Tag (Cat. No. TSR-H525a) on Protein A Biosensor, can bind Human TSLP Protein (R127A, R130A), His Tag (Cat. No. TSP-H5243) with an affinity constant of 23 nM as determined in BLI assay (ForteBio Octet R8) (Routinely tested).

Protocol

TSLP R BLI

Loaded Human TSLP R, Fc Tag (Cat. No. TSR-H525a) on Protein A Biosensor, can bind Biotinylated Human TSLP, His,Avitag (Cat. No. TSP-H82Eb) with an affinity constant of 13.2 nM as determined in BLI assay (ForteBio Octet R8)(Routinely tested).

Protocol

TSLP R BLI

Loaded Human TSLP R, Fc Tag (Cat. No. TSR-H525a) on Protein A Biosensor, can bind Biotinylated Human TSLP (R127A, R130A) Protein, His,Avitag (Cat. No. TSP-H82E0) with an affinity constant of 9.67 nM as determined in BLI assay (ForteBio Octet R8) (Routinely tested).

Protocol

 
评论(3)
  1. 182XXXXXXX6
  2. 0人赞
  3. 首次用到TSLP R重组蛋白,首先还是ACRO,主要用于抗体活性检测。蛋白活性经得起验证,在多次重复实验中,所得到的数据结果都高度一致,这让我们对后续实验的开展充满了信心,也使得我们的研究成果更具可信度,支持ACRO。
  4. 2025-2-20
  1. 199XXXXXXX5
  2. 0人赞
  3. 使用过多款ACRO的TSLP蛋白了,人猴不同种属的蛋白质量都很nice,本次使用TSLP R蛋白主要用于单克隆抗体BLI活性检测,蛋白活性很高,用先固化蛋白再与抗体结合的方式检测的,数据拟合结果完全符合预期,值得点赞。
  4. 2025-2-10
  1. 137XXXXXXX4
  2. 0人赞
  3. TSR-H525a 的这个抗原亲测非常有用,几次检测亲和力结果都很稳定,数据重复率很高,推荐推荐!!
  4. 2021-11-10
 
ACRO质量管理体系
 
 

背景(Background)

Receptor for thymic stromal lymphopoietin (TSLP). CRLF2 / TSLPR is a member of the type I cytokine receptor family. Together with the interleukin 7 receptor (IL7R) and TSLP activate STAT3, STAT5, and JAK2 pathways, which control processes such as cell proliferation and development of the hematopoietic system.

 

前沿进展

Ascorbic Acid Encapsulated in Apoferritin as Improved Protoporphyrin-Sensitized TiO2 Nanoarrays of a Photoelectrochemical Nanobody-Based Microfluidic Biosensor for Immunoassay
Yu, Wang, Jia et al
Anal Chem (2025) 97 (11), 6067-6074
Abstract: In this work, a nanobody-based microfluidic photoelectrochemical sensor utilizing protoporphyrin-sensitized TiO2 nanoarrays as signal transducer was developed for the detection of thymic stromal lymphopoietin (TSLP), a typical biomarker of asthma. The TiO2 nanoarrays were fabricated on ITO substrates via magnetron sputtering and in situ oxidation, and their visible light absorption and photogenerated carrier properties were improved upon sensitization with protoporphyrin dye. The electron donor ascorbic acid (AA) was encapsulated within apoferritin (ApoFt) and coupled directly to the target TSLP to obtain the ApoFt@AA-TSLP bioconjugate, which was subsequently mixed with different concentrations of TSLP and added to the electrode surface, enabling the quantitative release of AA dependent on the disassembly/reassembly properties of the ferritin shell. The detection process was integrated into a miniaturized microfluidic sensor chip to prevent biomolecular leakage at the sensing interface. Notably, nanobodies were employed in this system instead of traditional monoclonal antibodies to counteract the loss of activity induced by strong alkaline stimulation of the epitope during AA release. The sensor is high specificity, stability, and reproducibility with a sensitive photoelectrochemical response to TSLP in a linear range of 1.00 ng/mL to 1.00 μg/mL and a limit of detection as low as 0.08 ng/mL, demonstrating its significant potential for detecting biomarkers of protein-related diseases.
Distinct roles for thymic stromal lymphopoietin (TSLP) and IL-33 in experimental eosinophilic esophagitis
Dsilva, Wagner, Itan et al
bioRxiv (2025)
Abstract: Thymic stromal lymphopoietin (TSLP) and IL-33 are alarmins implicated in EoE pathogenesis by activating multiple cells including mast cells (MCs). Whether TSLP or IL-33 have a role in EoE and whether their activities are distinct requires further investigation.Experimental EoE was induced in wild type (WT) Il33 -/- and Crlf2 -/- mice. TSLP or IL-5 were neutralized using antibodies. Esophageal histopathology was determined by H&E, anti-Ki67, anti-CD31 and anti-MBP staining. Esophageal RNA was subjected to RNA sequencing. Bone marrow-derived MCs were activated with TSLP and IL-13 was determined (ELISA).TSLP and IL-33 were overexpressed in human and experimental EoE. Human and mouse esophageal MCs displayed the highest level of Crlf2 (TSLPR) compared to other immune cells. Crlf2 -/- mice were nearly-completely protected from EoE, and TSLP neutralization resulted in decreased basal cell proliferation, eosinophilia, lamina propria thickening and vascularization. Induction of experimental EoE in Il33 -/- mice resulted in reduced eosinophilia but no alterations in tissue remodeling were observed compared to WT mice. RNA sequencing revealed that TSLP regulates the expression of key genes associated with human EoE (e.g. eotaxins, Il19, Klk5, Flg, Il36rn, Il1r2) and suggest a role for TSLP in regulating IL-1 signaling, barrier integrity and epithelial cell differentiation. Experimental EoE was characterized by a MC-associated gene signature and elevated MCs. Activation of MCs with TSLP resulted in secretion of IL-13.TSLP and IL-33 have non-redundant functions in experimental EoE. This study highlights TSLP as an upstream regulator of IL-13 and a potential therapeutic target for EoE.
Tezepelumab inhibits highly functional truncated thymic stromal lymphopoietin in chronic rhinosinusitis
Oka, Klingler, Kidoguchi et al
J Allergy Clin Immunol (2025)
Abstract: Thymic stromal lymphopoietin (TSLP) and its functional cleavage products are elevated in nasal polyps (NPs) and play important roles in type 2 (T2) inflammation in chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP) by activating myeloid dendritic cells (mDCs) and group 2 innate lymphoid cells (ILC2s). However, whether tezepelumab, a human mAb against TSLP, inhibits functional cleaved TSLP and also the role of TSLP in CRS without nasal polyps (CRSsNP) have not yet been studied.We sought to investigate the effects of tezepelumab on cleaved TSLP in CRS.The mRNA expression levels for TSLP and T2 markers in ethmoid tissues (ETs) from 31 controls and 118 patients with CRSsNP and in NPs from 53 patients with CRSwNP were measured by quantitative RT-PCR. Cleaved TSLP was prepared from full-length recombinant TSLP by incubation with tissue extracts of NPs and CRSsNP ETs. The effects of tezepelumab on cleaved TSLP-induced inflammation were evaluated using PBMCs by monitoring the production of chemokines (CCL17 and CCL22 for mDCs) and cytokines (IL-5 and IL-13 for ILC2s).The mRNA expression level of TSLP was elevated not only in NPs but also in ETs from T2 CRSsNP compared with non-T2 CRSsNP and controls, and was positively correlated with T2 markers in CRSsNP (P < .001). CRSsNP ET also truncated and created highly active TSLP products. The activation of mDCs and ILC2s by full-length TSLP and cleaved TSLP created by ET and NP extracts was dose-dependently inhibited by tezepelumab.TSLP plays a role in T2 inflammation in CRSsNP and CRSwNP. Treatment with tezepelumab may benefit patients with T2 CRS by inhibiting active forms of TSLP.Copyright © 2025 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Sex disparity in adult asthma-A potential immunomodulatory role of let-7 family microRNAs
Malmhäll, Calvén, Weidner et al
Clin Transl Allergy (2025) 15 (3), e70042
Abstract: Sex differences have been reported in the incidence, prevalence and severity of asthma. Previous findings from animal models have revealed sex-related differences in inflammatory pathways that may contribute to asthma pathogenesis, but human studies are limited.Airway and blood samples (n = 55 and n = 85 respectively) were collected from adult females and males with asthma and healthy subjects. Type 2 innate lymphoid cells (ILC2s), T helper (Th)2 cells and their expression of IL-33R/ST2 (ST2L) were evaluated by flow cytometry. IL-13, thymic stromal lymphopoietin (TSLP), IL-33 and soluble IL-33R/ST2 (sST2) were measured by ELISA. Let-7 miRNA expression in bronchial biopsies was determined by qPCR.Females with asthma reported more exacerbations and had a higher number of airway eosinophils compared with males with asthma. Bronchial biopsy expression of Let-7f, Let-7g and miR-98 tended to be higher in males with asthma compared with females and inversely correlated with asthma exacerbations. In contrast, increased levels of IL-13, TSLP and sST2 were found in females with asthma compared with males.Our study demonstrates different inflammatory signatures between males and females with asthma. Let-7 miRNAs act as immune modulators by inhibiting the production of IL-13 and may be an important factor explaining the sex disparity seen in asthma.© 2025 The Author(s). Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology.
Showing 1-4 of 192 papers.
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TSLP R靶点信息
英文全称:Thymic stromal lymphopoietin
中文全称:胸腺基质淋巴细胞生成素
种类:Homo sapiens
上市药物数量:1详情
临床药物数量:23详情
最高研发阶段:批准上市
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