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Anti-CD3 epsilon Antibody [OKT3] (PE)

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Anti-CD3 epsilon Antibody [OKT3] (PE) este un anticorp monoclonal de șoarece împotriva țintei CD3 epsilon, cu reactivitate declarată pentru Human. Este validat pentru Flow Cytometry, are izotipul IgG2a și este conjugat cu PE. Se livrează în mărimea 100T, la prețul de 3.593,70 lei cu TVA.

Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.

Descriere

Mouse monoclonal [OKT3] antibody to CD3 epsilon (PE).

Specificații

Mărime
100T
Applications
Flow Cytometry
Reactivity
Human
Conjugate
PE
Host
Mouse
Clonality
Monoclonal
Product form
Liquid
Concentration
100 µg/ml
Isotype
IgG2a
Clonă
OKT3
Imunogen
Human peripheral blood lymphocytes.
Specificitate
This antibody recognises T-cell surface glycoprotein CD3 epsilon chain (CD3e), also known as T-cell surface antigen T3/Leu-4 epsilon. CD3e is a subunit within the multiprotein cell surface receptor TCR-CD3 complex, which is expressed on the surface of mature T cells, NKT cells and thymocytes. The CD3 complex is required for intracellular signaling and for TCR surface expression. Recruitment of the TCR/CD3 complex initiates early events leading to proliferation and differentiation of mature T cells into an effector cell. Mice that lack the CD3e gene exhibit early arrest in T cell development and mutation of the gene in humans has been seen to result in severe combined immunodeficiency (SCID) (DeJarnette et al. 1998, de Saint Basile et al. 2004). Mouse anti Human CD3, clone OKT3 is commonly used in flow cytometry in the phenotyping human T cells. Characterization of the OKT3 clone has shown that it is able to compete and block the binding of the CD3 clones SK7 and UCHT1 to human T cells. The OKT3 clone has also been found to have immunosuppressive properties in vivo. As result of this, the clone was humanized to be used as a therapeutic drug called Muromonomab (Orthoclone). Muromonomab was used as an immunosuppressive including for after solid organ transplants, to prevent the activation of CD4- and CD8- T cells. However, the drug has since been discontinued due to the development of other treatments with similar efficacy and fewer side effects (Reichert 2012).

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