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Research Grade Anti-Human ATTR/Transthyretin amyloidosis Antibody (NI-301)

Catalog #:   DHC01301 Specific References (50) DATASHEET
Host species: Human
Isotype: IgG
Applications: Research Grade Biosimilar
Expression system: Mammalian Cells
Overview

Catalog No.

DHC01301

Expression system

Mammalian Cells

Species reactivity

Human

Host species

Human

Isotype

IgG

Clonality

Monoclonal

Target

Transthyretin, Prealbumin, TBPA, TTR, PALB, ATTR

Concentration

1 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

P02766

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

NI-301, NI 301, NI301

Clone ID

NI-301

Data Image
References

Current and emerging treatment options for transthyretin amyloid cardiomyopathy., PMID:40425273

Current Landscape of Therapies for Transthyretin Amyloid Cardiomyopathy., PMID:40335224

Etiological Treatment of Cardiac Amyloidosis: Standard of Care and Future Directions., PMID:40232627

Concurrent Therapy for Immunoglobulin Light Chain Cardiac Amyloidosis and Transthyretin Cardiac Amyloidosis: A Case Report., PMID:39924245

Transthyretin Cardiac Amyloidosis: Current and Emerging Therapies., PMID:39841315

New therapies to treat cardiac amyloidosis., PMID:39819772

Advancing treatments for transthyretin amyloid cardiomyopathy: Innovations in RNA silencing, gene editing, TTR stabilization, and degradation., PMID:39775625

Disease-modifying therapies for amyloid transthyretin cardiomyopathy: Current and emerging medications., PMID:39714070

Pathogenesis, manifestations, diagnosis, and management of CNS complications in hereditary ATTR amyloidosis., PMID:39627935

Transthyretin Cardiac Amyloidosis in Australia and New Zealand-A Multi-Site Snapshot for 2022., PMID:39592278

Optimizing drug therapies in cardiac amyloidosis., PMID:39586360

Evolving Strategies in Cardiac Amyloidosis: From Mechanistic Discoveries to Diagnostic and Therapeutic Advances., PMID:39551565

PRX004 in variant amyloid transthyretin (ATTRv) amyloidosis: results of a phase 1, open-label, dose-escalation study., PMID:39472768

Prediction of Cardiac ATTR Depletion by NI006 (ALXN2220) Using Mechanistic PK/PD Modeling., PMID:39410666

Structural Basis for Monoclonal Antibody Therapy for Transthyretin Amyloidosis., PMID:39338387

[Clinical case of generalized amyloidosis (ATTR-amyloidosis) with a progressive course of chronic heart failure. Case report]., PMID:39106513

Recent advances in the diagnostic methods and therapeutic strategies of transthyretin cardiac amyloidosis., PMID:39086890

Antithrombotic properties of Tafamidis: An additional protective effect for transthyretin amyloid cardiomyopathy patients., PMID:39029855

Specific Therapy in Transthyretin Amyloid Cardiomyopathy: Future Perspectives Beyond Tafamidis., PMID:38844305

Current Therapies and Future Horizons in Cardiac Amyloidosis Treatment., PMID:38809394

Identification of isoaspartate-modified transthyretin as potential target for selective immunotherapy of transthyretin amyloidosis., PMID:38801321

Treatment of transthyretin cardiac amyloidosis., PMID:38652263

Detection of TTR Amyloid in the Conjunctiva Using a Novel Fluorescent Ocular Tracer., PMID:38359019

Molecular mechanisms and emerging therapies in wild-type transthyretin amyloid cardiomyopathy., PMID:38233673

Breakthrough advances enhancing care in ATTR amyloid cardiomyopathy., PMID:38184468

Epidemiological study of the subtype frequency of systemic amyloidosis listed in the Annual of the Pathological Autopsy Cases in Japan., PMID:38088470

Pathomorphological Features of the Novel Coronavirus Disease in Patients with Systemic Amyloidosis., PMID:37893183

Randall-Type Monoclonal Immunoglobulin Deposition Disease in Bone Scintigraphy., PMID:37883135

Development and characterization of a prototypic pan-amyloid clearing agent - a novel murine peptide-immunoglobulin fusion., PMID:37854603

Coronary artery bypass grafting for triple vessel disease in cardiac amyloidosis., PMID:37699742

Strong positive light chain immunostaining in a patient with transthyretin amyloidosis., PMID:37551718

RNAi therapeutics for diseases involving protein aggregation: fazirsiran for alpha-1 antitrypsin deficiency-associated liver disease., PMID:37470509

Mapping cellular response to destabilized transthyretin reveals cell- and amyloidogenic protein-specific signatures., PMID:37439769

Antibody-Associated Reversal of ATTR Amyloidosis-Related Cardiomyopathy., PMID:37285532

Phase 1 Trial of Antibody NI006 for Depletion of Cardiac Transthyretin Amyloid., PMID:37212440

Treatment of amyloidosis: present and future., PMID:37091663

Steep increase in the number of transthyretin-positive cardiac biopsy cases in Japan: evidence obtained by the nation-wide pathology consultation for the typing diagnosis of amyloidosis., PMID:36795075

Monoclonal Gammopathy of Undetermined Significance in Patients With Transthyretin Amyloidosis (ATTR): Analysis Using the iStopMM Criteria., PMID:36621346

Current approaches to the diagnosis and management of amyloidosis., PMID:36478370

Dual Targeting of Soluble Oligomeric and Aggregated Transthyretin with a Monoclonal Antibody Ameliorates Experimental Neuropathy., PMID:36290413

Treatment of Transthyretin Amyloid Cardiomyopathy: The Current Options, the Future, and the Challenges., PMID:35456241

Cardiac Amyloidosis Treatment., PMID:35414852

Circulating biomarkers in diagnosis and management of cardiac amyloidosis: a review for internist., PMID:35325395

Cardiac microcalcifications in transthyretin (ATTR) amyloidosis., PMID:35077727

Developing Therapy for Transthyretin Amyloidosis., PMID:35077703

Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease., PMID:34814699

Pathological review of cardiac amyloidosis using autopsy cases in a single Japanese institution., PMID:34653913

[Heart damage in the combined types of systemic amyloidosis]., PMID:34609800

Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment., PMID:34443678

Immunohistochemical typing of amyloid in fixed paraffin-embedded samples by an automatic procedure: Comparison with immunofluorescence data on fresh-frozen tissue., PMID:34428239

Datasheet
$ 328
Product specifications
100 μg 328 1 mg 1314

Contact Information

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Distributor list

For research use only. Not for human or drug use.

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Research Grade Anti-Human ATTR/Transthyretin amyloidosis Antibody (NI-301) [DHC01301]
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