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Rekombinanter PDCD1 (Camrelizumab Biosimilar) Antikörper

Dieser Humanized Monoklonal Antikörper detektiert spezifisch PDCD1 (Camrelizumab Biosimilar) in FACS und in vivo. Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7795091
-15% Promotion 2026
237,02 €
278,85 €
Sparen Sie 41,83 € (-15 %)
Zzgl. Versandkosten 20,00 € und MwSt
1 mg
Lieferung nach: Deutschland
Lieferung in 25 bis 31 Werktagen

Kurzübersicht für Rekombinanter PDCD1 (Camrelizumab Biosimilar) Antikörper (ABIN7795091)

Target

PDCD1 (Camrelizumab Biosimilar)

Antikörpertyp

Recombinant Antibody

Reaktivität

Human

Wirt

  • 1
  • 1
  • 1
Humanized

Klonalität

  • 2
  • 1
Monoklonal

Konjugat

  • 3
Dieser PDCD1 (Camrelizumab Biosimilar) Antikörper ist unkonjugiert

Applikation

  • 2
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS), In vivo Studies (in vivo)

Güteklasse

Research Grade
  • Expressionssystem

    Mammalian cells

    Verwendungszweck

    Camrelizumab Biosimilar, PD-1 Monoclonal Antibody

    Produktmerkmale

    Camrelizumab Biosimilar uses the same protein sequences as the therapeutic antibody camrelizumab. Camrelizumab is an IgG4κ humanized monoclonal antibody being investigated for hepatocellular carcinoma. It targets programmed cell death protein 1 (PD-1), a protein on the surface of cells, also known as CD279 (cluster of differentiation 279). Camrelizumab is being evaluated in the Phase 2/3 (NCT02989922) of patients with advanced hepatocellular carcinoma (HCC) in second-line after failure or intolerance to prior systemic treatment. The study has 2 arms in which patients will be intravenous administered 3 mg/kg SHR-1210 on day 1 every 2 weeks or every 3 weeks. The primary outcome measures are the overall response rate (ORR) and overall survival (OS) rates at 6 months with duration of response and OS at 2 years as secondary endpoints. The estimated enrollment is 220 patients, and the estimated primary completion date is December 2018. A randomized, open-label Phase 3 study (NCT03099382) is evaluating the efficacy of camrelizumab treatment compared to standard-of-care treatment (docetaxel or irinotecan) in patients with esophageal carcinoma. Patients are randomly assigned to receive either SHR-1210 (200 mg every 2 weeks) or the standard of care (docetaxel 75 mg/m2 on day 1 every 3 weeks or irinotecan 180 mg/m2 on day 1 every 2 weeks). This Phase 3 study has an estimated enrollment of 438 and an estimated primary completion date of June 2018.

    Aufreinigung

    Protein A or G affinity column

    Reinheit

    >95 % by reducing SDS-PAGE

    Endotoxin-Niveau

    < 1 EU per 1 mg of the protein by the LAL method

    Immunogen

    Human PD1
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    > 3 mg/mL

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

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

    PDCD1 (Camrelizumab Biosimilar)

    Andere Bezeichnung

    Camrelizumab Biosimilar

    Substanzklasse

    Biosimilar
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