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    首頁(yè) /藥靶模型 /免疫治療 /Combination /SIRPɑ&PD1 Dual Effector Reporter Cell

    SIRPɑ&PD1 Dual Effector Reporter Cell

    CBP74154

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    I. Background
    SIRP alpha protein, or Signal regulatory proteinalpha (SIRP-α), also known as Tyrosine protein phosphatase non-receptor type substrate 1, CD172a, Bit, and MyD-1, GenBank Accession No. NM_080792, a.a. 27-370, with C-terminal Avi and His tags, MW 40.3 kDa*. This SIRP alpha protein acts as a receptor for CD47; a.a. 27-370 correspond to the extracellular portion of SIRP-α. *Note: SIRP-α is heavily glycosylated, resulting in higher molecular weight.

     

    The binding of Programmed Cell Death Protein 1 (PD-1), a receptor expressed on activated T-cells, to its ligands, PD-L1 and PD-L2, negatively regulates immune responses. PD-1 ligands are found on most cancers, and the PD-1:PD-L1/2 interaction inhibits T-cell activity and enables cancer cells to escape immune surveillance. The PD-1:PD-L1/2 pathway is also involved in regulating autoimmune responses, making these proteins promising therapeutic targets for a number of cancers, as well as multiple sclerosis, arthritis, lupus, and type I diabetes

     
    II. Introduction
    Expressed gene: SIRPɑ、PD-1
    Stability: 32 passages(in-house test, that not means the cell line will be instable beyond the passages we tested.)
    Synonym(s): SIRPɑ、PD-1
    Freeze Medium: 90% FBS+10% DMSO
    Culture Medium: RPMI-1640+10%FBS+2ug/ml puromycin+5ug/ml blasticidin+ 200ug/ml hygromycin
    Mycoplasma Testing: Negative
    Storage: Liquid nitrogen
    Application(s): Functional(Report Gene) Assay
     
    III. Representative Data

    Figure 1. Dose response of Blocking Antibodies in SIRPα/PD-1 Dual Effector Reporter Cells(C18) With CD47/PD-L1 Dual Target Cells.

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