Anti-Human CD3 x CD19 (Blinatumomab) [Clone AMG103],Leinco,C2530

Host

Human

Reactivity

Human

Platform ID

BAB384266940

Leinco

Headquarters

410 Axminister Drive St. Louis, Missouri 63026

Contact

Tel: +1 (800) 538-1145,+1 (636) 230-9477
Fax:

Product Specifications
Scientific Background

Specifications

NameAnti-Human CD3 x CD19 (Blinatumomab) [Clone AMG103]
Cat. No.C2530
HostHuman
ReactivityHuman
Concentration≥ 5.0 mg/ml
ImmunogenCD19 murine parental clone is HD37. CD3E murine parental clone is L2K-07.
Purity≥95% by SDS Page ⋅ ≥95% monomer by analytical SEC
Endotoxin Level≤ 1.0 EU/mg as determined by the LAL method
Shipping2 – 8° C Wet Ice
FormulationThis biosimilar antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
StorageFunctional grade biosimilar antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at -80°C. Avoid Repeated Freeze Thaw Cycles.

Scientific Background

Blinatumomab is a Bispecific T cell Engager (BiTE) antibody developed as a cancer immunotherapeutic drug 1,2,3,4 . Blinatumomab induces apoptosis of target B cells by binding simultaneously to the C19 surface antigen of all B cells (healthy and malignant) as well as the epsilon subunit of the CD3 invariant antigen of the T cell TCR (T cell receptor) 4 . Binding is achieved via two large single-chain variable fragments arranged in tandem, with the CD19-binding fragment at the N-terminal and the CD3 binding fragment at the C-terminal. The fragments are linked by a flexible, non-immunogenic, non-glycosylated five amino acid peptide (four glycine and one serine), which confers a high degree of rotational flexibility to facilitate simultaneous epitope binding. In this way, blinatumomab targets malignant B cells for apoptosis via CD19, a B-lymphocyte-specific receptor responsible for promoting activation and differentiation of normal B cells that functions as a costimulatory molecule of the B cell receptor 2 . Blinatumomab binding forces the colocalization of cytotoxic T lymphocytes and B cells expressing CD19 4 . A structurally normal cytolytic immune synapse is formed, and, in T cells, activation events trigger the delivery of granzyme and perforin into the synaptic space, inducing apoptosis of the targeted B cells. Recruitment and activation of T cells occurs after the second arm of blinatumomab binds to the target cell antigen. An activated T cell can kill several B cells. Blinatumomab is a B lineage-specific antitumor mouse monoclonal antibody 4 . The CD19-targeting fragment is derived from the parental murine monoclonal antibody HD37, while the CD3-binding fragment is derived from the parental murine monoclonal antibody L2K-07 1,3,4 . Blinatumomab is only one-third the size of traditional antibodies at 504 amino acids and a molecular weight of 55 kDa 4 . Other names for blinatumomab are MT103, MEDI‐538, bscCD19xCD3, and AMG103. Blinatumomab is a non-glycosylated fusion protein.

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