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Recombinant CD274 (Atezolizumab Biosimilar) antibody

The Humanized Monoclonal anti-CD274 (Atezolizumab Biosimilar) antibody has been validated for FACS and in vivo. It is suitable to detect CD274 (Atezolizumab Biosimilar) in samples from Human.
Catalog No. ABIN7795089

Quick Overview for Recombinant CD274 (Atezolizumab Biosimilar) antibody (ABIN7795089)

Target

CD274 (Atezolizumab Biosimilar)

Antibody Type

Recombinant Antibody

Reactivity

Human

Host

  • 13
  • 1
Humanized

Clonality

  • 13
  • 1
Monoclonal

Conjugate

  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CD274 (Atezolizumab Biosimilar) antibody is un-conjugated

Application

  • 12
  • 11
  • 9
  • 1
Flow Cytometry (FACS), In vivo Studies (in vivo)

Grade

Research Grade
  • Expression System

    Mammalian cells

    Purpose

    Atezolizumab Biosimilar, Endotoxin 0.05 EU/mg

    Characteristics

    What is Atezolizumab biosimilar research grade? Atezolizumab is a humanized monoclonal antibody directed against the human protein ligand PD-L1, with potential immune checkpoint inhibitory and antineoplastic activities. Atezolizumab is an Fc-engineered, humanized, monoclonal antibody (IgG1κ isotype). Atezolizumab biosimilar uses the same protein sequences as the therapeutic antibody atezolizumab. Atezolizumab lacks the N-glycosylation site in its Fc region by changing an aspartic acid into alanine at amino acid position 298 (amino acid position 297 according to EU nomenclature, N297A) in the heavy chain leading to minimized binding to FcγRs. PD-L1 (B7-H1 or CD274, programmed cell death ligand 1) and PD-L2 (B2-DC or CD273, programmed cell death ligand 2) are the two ligands for the receptor PD-1 (CD279, programmed death 1). PD-L1 is an immune checkpoint molecule expressed on both tumor cells and certain immune cells. The binding of PD-L1 to its receptors PD-1 or B7.1 on activated T cells causes an inhibitory signal to suppress their production in the lymph nodes, thereby preventing immune responses to events such as pregnancy or autoimmune disease. This pathway is also utilized by cancer cells to evade the immune system through evasion of anti-tumor T-cell response. Furthermore, over-expression of PD-L1 and PD-1 has been linked to increased tumor aggressiveness and poorer prognosis. Atezolizumab binds directly and selectively to PD-L1 and blocks interaction with both PD-1 and B7.1 receptors, thus reinvigorates and enhances the body's adaptive anti-cancer activity. Disrupting the PD-L1/B7.1 interaction may also enhance T-cell priming, which could result in increased duration of response and survival.

    Purification

    Protein A or G affinity column

    Purity

    >95 % by reducing SDS-PAGE

    Endotoxin Level

    Less than 0.5 EU/mg of protein as determined by LAL method

    Immunogen

    Human PD-L1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    > 3 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    Short time 2 to 8°C as supplied. Long time -20°C to -70°C as supplied.
  • Target

    CD274 (Atezolizumab Biosimilar)

    Alternative Name

    Atezolizumab Biosimilar

    Target Type

    Biosimilar
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