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Research Grade Luspatercept

Catalog #:   DHB63001 Specific References (49) DATASHEET
Isotype: Fusion - [ACVR2B (activin A receptor type 2B, ActR-IIB, ActRIIB)]2 - IGHG1 Fc (Fragment constant)
Applications: Research Grade Biosimilar
Expression system: Mammalian Cells
Accession: O95390
Overview

Catalog No.

DHB63001

Expression system

Mammalian Cells

Species reactivity

Human

Isotype

Fusion - [ACVR2B (activin A receptor type 2B, ActR-IIB, ActRIIB)]2 - IGHG1 Fc (Fragment constant)

Target

GDF11, BMP-11, BMP11, Growth/differentiation factor 11, GDF-11, Bone morphogenetic protein 11

Concentration

7 mg/ml

Endotoxin level

Please contact with the lab for this information.

Purity

>95% as determined by SDS-PAGE.

Purification

Protein A/G purified from cell culture supernatant.

Accession

O95390

Applications

Research Grade Biosimilar

Form

Liquid

Storage buffer

0.01M PBS, pH 7.4.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term.

Alternative Names

ACE-536,luspatercept–aamt, CAS: 1373715-00-4

Clone ID

Luspatercept

Data Image
  • SDS-PAGE
    SDS PAGE for Luspatercept
References

Combined detection of inhibitors of the activin receptor signaling pathways (IASPs) by means of LC-HRMS/MS for human doping control., PMID:40481031

Luspatercept for the treatment of lower-risk myelodysplastic syndrome with SF3B1 mutation: a real-world single-center research in China., PMID:40474348

Efficacy of erythroid-stimulating agent and luspatercept in VEXAS syndrome: A multicenter retrospective study by the FRENVEX group., PMID:40469482

Navigating the dynamic landscape of lower-risk MDS: Advances and emerging insights., PMID:40450506

Splicing of erythroid transcription factor is associated with therapeutic response in myelodysplastic syndromes., PMID:40424086

Luspatercept in lower-myelodysplastic syndromes (MDS): Real-world data from the Gruppo Romano-Laziale Mielodisplasie (GROM-L) and review of literature., PMID:40383062

Long-Term Transfusion Independence with Luspatercept Versus Epoetin Alfa in Erythropoiesis-Stimulating Agent-Naive, Lower-Risk Myelodysplastic Syndromes in the COMMANDS Trial., PMID:40377899

The double edge of erythropoietic modulation in thalassaemia., PMID:40364548

New Approvals in Low- and Intermediate-Risk Myelodysplastic Syndromes., PMID:40334184

Healthcare resource utilization of patients with lower-risk myelodysplastic syndromes treated with luspatercept versus erythropoiesis-stimulating agents: a United States healthcare claims database study., PMID:40329816

Real-life experience of luspatercept in transfusion-dependent lower risk myelodysplastic syndrome patients., PMID:40325906

How to use luspatercept and erythropoiesis-stimulating agents in low-risk myelodysplastic syndrome., PMID:40318055

Emerging Therapeutic Approaches for Anemia in Myelofibrosis., PMID:40317385

Gel Electrophoretic Detection of Black Market ACE-031., PMID:40312924

Acute splenomegaly, haemolysis, and thrombocytopenia following luspatercept initiation in a patient with transfusion-dependent thalassaemia: A case report., PMID:40307204

Contemporary management paradigms and emerging therapeutics for myelodysplastic syndromes/neoplasms., PMID:40302714

Imatinib-Induced Clinical Response in ETV6::ACSL6 Myeloid Neoplasm with Eosinophilic Pneumonitis: A Case Report., PMID:40200571

Managing Myelofibrosis: Matching Advances in Treatments With Clinical Unmet Needs., PMID:40192154

A challenging convergence of conditions in a patient with thalassemia major presenting with thymoma and lymphangioleiomyomatosis: a case report., PMID:40134035

Low-risk MDS-A spotlight on precision medicine for SF3B1-mutated patients., PMID:40124717

Emerging Pathogenetic Mechanisms and New Drugs for Anemia in Myelofibrosis and Myelodysplastic Syndromes., PMID:40056069

Real world efficacy of luspatercept in patients with lower-risk myelodysplastic syndromes/neoplasms (MDS); a single center study in a heavily pretreated cohort., PMID:40053838

Long-Term Experience with Luspatercept in Relapsed/Refractory Myelodysplastic Neoplasms: A Chinese Real-World Study., PMID:40025395

Safety and efficacy of luspatercept in treating anemia associated with myelodysplastic syndrome with ring sideroblasts in Asian patients who require red blood cell transfusions: a phase II bridging study., PMID:39991012

What we now BELIEVE is achievable with luspatercept in transfusion-dependent β-thalassaemia., PMID:39947216

Long-term efficacy and safety of luspatercept for the treatment of anaemia in patients with transfusion-dependent β-thalassaemia (BELIEVE): final results from a phase 3 randomised trial., PMID:39947215

Response to luspatercept can be predicted and improves overall survival in the real-life treatment of LR-MDS., PMID:39944234

Post-marketing safety concerns with luspatercept: a disproportionality analysis of the FDA adverse event reporting system., PMID:39912511

Luspatercept for the treatment of anemia in allo-HSCT for patients with hematological diseases., PMID:39910033

Advancing drug development in myelodysplastic syndromes., PMID:39786387

Sex and Gender Differences in Iron Chelation., PMID:39767791

[Luspatercept as first line in transfusion-dependant very low to intermediate risk myelodysplastic syndromes]., PMID:39706724

Luspatercept in β-thalassemia: Who and when. Strengths and weaknesses points of a real-world evidence., PMID:39691262

Iron overload in acquired sideroblastic anemias and MDS: pathophysiology and role of chelation and luspatercept., PMID:39644054

Luspatercept: a treatment for ineffective erythropoiesis in thalassemia., PMID:39644029

Treatment of high-risk myelodysplastic syndromes., PMID:39633555

Real-world impact of luspatercept on red blood cell transfusions among patients with myelodysplastic syndromes: A United States healthcare claims database study., PMID:39602855

Beta Thalassemia in Children: Established Approaches, Old Issues, New Non-Curative Therapies, and Perspectives on Healing., PMID:39598110

A phase 2 clinical trial of luspatercept in non-transfusion-dependent patients with myelodysplastic syndromes., PMID:39572468

[Current treatment options for lower-risk myelodysplastic neoplasms]., PMID:39505558

[Migration Medicine: infectious and non-infectious diseases]., PMID:39437825

Genetic iron overload aggravates, and pharmacological iron restriction improves, MDS pathophysiology in a preclinical study., PMID:39437711

Experience with luspatercept therapy in patients with transfusion-dependent low-risk myelodysplastic syndromes in real-world clinical practice: exploring the positive effect of combination with erythropoietin alfa., PMID:39416466

Real-life data of luspatercept in lower-risk myelodysplastic syndromes advocate new research objectives., PMID:39415916

Beyond HMAs: Novel Targets and Therapeutic Approaches., PMID:39389839

Targeted therapies for myelodysplastic syndromes/neoplasms (MDS): current landscape and future directions., PMID:39367718

[Novel therapies for MDS and future prospects]., PMID:39358299

Is luspatercept the new standard of care in transfusion-dependent low-risk myelodysplastic syndromes?, PMID:39356814

Real-world efficacy and safety of luspatercept and predictive factors of response in patients with transfusion-dependent β-thalassemia., PMID:39264036

Datasheet

Document Download

Research Grade Luspatercept.pdf

 

$ 426
Product specifications
100 μg 426 1 mg 1704

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Research Grade Luspatercept [DHB63001]
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