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 >  Protein>SIRP alpha >SIA-H52A8

Human SIRP alpha / CD172a Protein, Mouse IgG1 Fc Tag (MALS verified)

分子别名(Synonym)

SHPS1,SIRPA,CD172A,BIT,MFR,MYD1,P84,PTPNS1

表达区间及表达系统(Source)

Human SIRP alpha, Mouse IgG1 Fc Tag (SIA-H52A8) is expressed from human 293 cells (HEK293). It contains AA Glu 31 - Arg 370 (Accession # NP_001035111).

Predicted N-terminus: Glu 31

Request for sequence

蛋白结构(Molecular Characterization)

SIRP alpha Structure

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

The protein has a calculated MW of 63.0 kDa. The protein migrates as 70-105 kDa 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 50 mM Tris, 100 mM Glycine, 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)

SIRP alpha SDS-PAGE

Human SIRP alpha, Mouse IgG1 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%.

SEC-MALS

SIRP alpha SEC-MALS

The purity of Human SIRP alpha, Mouse IgG1 Fc Tag (Cat. No. SIA-H52A8) is more than 90% and the molecular weight of this protein is around 140-165 kDa verified by SEC-MALS.

Report

 

活性(Bioactivity)-ELISA

SIRP alpha ELISA

Immobilized Human CD47, His Tag (Cat. No. CD7-H5227) at 2 μg/mL (100 μL/well) can bind Human SIRP alpha, Mouse IgG1 Fc Tag (Cat. No. SIA-H52A8) with a linear range of 4-31 ng/mL (QC tested).

Protocol

SIRP alpha ELISA

Serial dilutions of Anti-Human CD47 Neutralizing Antibody were added into Human SIRP alpha, Mouse IgG1 Fc Tag (Cat. No. SIA-H52A8): Biotinylated Human CD47, Fc,Avitag (Cat. No. CD7-H82F6) binding reactions. The half maximal inhibitory concentration (IC50) is 0.2006 μg/mL (Routinely tested).

Protocol

 

活性(Bioactivity)-FACS

SIRP alpha FACS

FACS assay shows that Human SIRP alpha, Mouse IgG1 Fc Tag (Cat. No. SIA-H52A8) can bind to Jurkat cell expressing CD47. The concentration of SIRP alpha used is 0.3 μg/mL (Routinely tested).

Protocol

SIRP alpha FACS

FACS analysis shows that the binding of Human SIRP alpha, Mouse IgG1 Fc Tag (Cat. No. SIA-H52A8) to Jurkat expressing CD47 was inhibited by increasing concentration of neutralizing anti-CD47 antibody. The concentration of SIRP alpha used is 0.3 μg/mL. IC50=0.1318 μg/mL (Routinely tested).

Protocol

 
评论(4)
  1. 173XXXXXXX3
  2. 1人赞
  3. 该产品用于药物功能筛选实验, 与阳性对照抗体、CD47+细胞以及ACRO的CD47-biotin具有很好的亲和力,用该蛋白对成功建立稳定的结合测试体系与RBA测试体系。
  4. 2021-10-13
  1. 166XXXXXXX7
  2. 1人赞
  3. 针对SIRP a靶点的项目,我们测试抗原抗体结合力强弱。筛选合适的分子进行下一步真核改造。同时还进行了多分子结合/表位竞争实验。
  4. 2021-9-24
  1. 139XXXXXXX9
  2. 1人赞
  3. 用于作为抗体筛选以及抗体功能的blocking实验,通过ELISA或者FACS希望得到能够与ligand有竞争关系的抗体,进行后续序列分析。
  4. 2021-10-14
 
ACRO质量管理体系
 
 

背景(Background)

Tyrosine-protein phosphatase non-receptor type substrate 1 (SHPS1) is also known as CD172 antigen-like family member A (CD172a), Macrophage fusion receptor, MyD-1 antigen, Signal-regulatory protein alpha (SIRPA or SIRP alpha) or p84, is a member of the SIRP family, and also belongs to the immunoglobulin superfamily. SIRP alpha is Ubiquitous and highly expressed in brain. SIRPA / CD172a is immunoglobulin-like cell surface receptor for CD47 and acts as docking protein and induces translocation of PTPN6, PTPN11 and other binding partners from the cytosol to the plasma membrane. SIRPA / SHPS-1 supports adhesion of cerebellar neurons, neurite outgrowth and glial cell attachment and may play a key role in intracellular signaling during synaptogenesis and in synaptic function By similarity. SIRPA / MyD1 involved in the negative regulation of receptor tyrosine kinase-coupled cellular responses induced by cell adhesion, growth factors or insulin and mediates negative regulation of phagocytosis, mast cell activation and dendritic cell activation. CD47 binding prevents maturation of immature dendritic cells and inhibits cytokine production by mature dendritic cells.

 

前沿进展

Maplirpacept: a CD47 decoy receptor with minimal red blood cell binding and robust anti-tumor efficacy
Krishnamoorthy, Seelige, Brown et al
Front Immunol (2025) 16, 1518787
Abstract: CD47 is highly expressed on cancer cells and triggers an anti-phagocytic "don't eat me" signal when bound by the inhibitory signal regulatory protein α (SIRPα) expressed on macrophages. While CD47 blockade can mitigate tumor growth, many CD47 blockers also bind to red blood cells (RBCs), leading to anemia. Maplirpacept (TTI-622, PF-07901801) is a CD47 blocking fusion protein consisting of a human SIRPα fused to an IgG4 Fc region and designed to limit binding to RBCs.To determine maplirpacept binding to RBCs and interference with blood tests, human blood samples were used. The ability of maplirpacept to promote macrophage-mediated phagocytosis of human tumor cells was assessed using both confocal microscopy and flow cytometry. In vivo antitumor efficacy as a monotherapy and in combination with other therapeutic agents was evaluated in xenograft models.In the current study, we demonstrate that maplirpacept has limited binding to RBCs while driving enhanced macrophage-mediated phagocytosis of hematological tumor cells in vitro and reducing tumor burden in human xenograft models. Moreover, phagocytosis of neoplastic cells can be enhanced when maplirpacept is combined with other therapeutic agents, including antibodies or chemotherapeutic agents.These preclinical results establish maplirpacept as an effective CD47 blocker that mitigates the potential for anemia in patients.Copyright © 2025 Krishnamoorthy, Seelige, Brown, Chau, Nielsen Viller, Johnson, Linderoth, Wang, Dillon, Abayasiriwardana, Lees, Wong, Kaneda, Uger and Lin.
Immunogenic Cell Death: the Key to Unlocking the Potential for Combined Radiation and Immunotherapy
Rauf, Smirnova, Chang et al
bioRxiv (2025)
Abstract: Immunogenic cell death (ICD) enhances anti-tumor immunity by releasing tumor-associated antigens and activating the anti-tumor immune system response. However, its potential remains understudied in combination therapies. Here, we develop a mathematical model to quantify the role of ICD in optimizing the efficacy of combined radiotherapy (RT) and macrophage-based immunotherapy. Using preclinical murine data targeting the SIRP α -CD47 checkpoint, we show that RT alone induces minimal ICD, whereas disrupting the SIRP α -CD47 axis significantly enhances both phagocytosis and systemic immune activation. Our model predicts an optimal RT dose (6-8 Gy) for maximizing ICD, a dose-dependent abscopal effect, and a hierarchy of treatment efficacy, with SIRP α -knockout macrophages exhibiting the strongest tumoricidal activity. These findings provide a quantitative framework for designing more effective combination therapies, leveraging ICD to enhance immune checkpoint inhibition and radiotherapy synergy.
Transcriptional activation of regenerative hematopoiesis via microenvironmental sensing
Itkin, Houghton, Schreiner et al
Nat Immunol (2025) 26 (3), 378-390
Abstract: Transition between activation and quiescence states in hematopoietic stem and progenitor cells (HSPCs) is tightly governed by cell-intrinsic means and microenvironmental co-adaptation. Although this balance is fundamental for lifelong hematopoiesis and immunity, the underlying molecular mechanisms remain poorly defined. Multimodal analysis divulging differential transcriptional activity between distinct HSPC states indicates the presence of Fli-1 transcription factor binding motif in activated hematopoietic stem cells. We reveal that Fli-1 activity is essential during regenerative hematopoiesis in mice. Fli-1 directs activation programs while priming cellular sensory and output machineries, enabling HSPCs co-adoptability with a stimulated vascular niche through propagation of niche-derived angiocrine Notch1 signaling. Constitutively induced Notch1 signaling is sufficient to recuperate functional hematopoietic stem cells impairments in the absence of Fli-1, without leukemic transformation. Applying FLI-1 transient modified-mRNA transduction into latent adult human mobilized HSPCs, enables their niche-mediated expansion and superior engraftment capacities. Thus, decryption of stem cell activation programs offers valuable insights for immunological regenerative medicine.© 2025. The Author(s), under exclusive licence to Springer Nature America, Inc.
Dual-mode action of scalable, high-quality engineered stem cell-derived SIRPα-extracellular vesicles for treating acute liver failure
Kim, Kim, Kim et al
Nat Commun (2025) 16 (1), 1903
Abstract: Acute liver failure (ALF) is a life-threatening condition caused by rapid hepatocyte death and impaired liver regeneration. Here we show that extracellular vesicles engineered to express Signal Regulatory Protein Alpha (SIRP-EVs), produced via a scalable 3D bioreactor process with high yield and purity, exhibit significant therapeutic potential by targeting damaged cells and promoting tissue repair. SIRP-EVs block CD47, a crucial inhibitory signal on necroptotic cells, to enhance macrophage-mediated clearance of dying hepatocytes. They also deliver regenerative cargo from mesenchymal stem cells, reprogramming macrophages to support liver regeneration. In male animal models, SIRP-EVs significantly reduce liver injury markers and improve survival, demonstrating their dual-function therapeutic efficacy. By integrating the resolution of necroptosis with regenerative macrophage reprogramming, SIRP-EVs represent a promising platform for restoring liver function. These findings support the development of EV-based in vivo macrophage reprogramming therapies for ALF and other inflammation-driven diseases, paving the way for the clinical application of engineered EV therapeutics.© 2025. The Author(s).
Showing 1-4 of 167 papers.
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SIRP alpha靶点信息
英文全称:Signal-regulatory protein alpha
中文全称:信号调节蛋白α
种类:Homo sapiens
上市药物数量:2详情
临床药物数量:18详情
最高研发阶段:批准上市
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