Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Recombinant PDCD1 (Camrelizumab Biosimilar) anticorps

Cet anticorps Humanized Monoclonal détecte spécifiquement PDCD1 (Camrelizumab Biosimilar) dans FACS et in vivo. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN7795091
-15% Promotion 2026
237,02 €
278,85 €
Économisez 41,83 € (-15 %)
Plus frais de livraison 40,00 € et TVA
1 mg
Destination: France
Envoi sous 25 à 31 jours ouvrables

Aperçu rapide pour Recombinant PDCD1 (Camrelizumab Biosimilar) anticorps (ABIN7795091)

Antigène

PDCD1 (Camrelizumab Biosimilar)

Type d'anticorp

Recombinant Antibody

Reactivité

Humain

Hôte

  • 3
  • 1
  • 1
Humanized

Clonalité

  • 4
  • 1
Monoclonal

Conjugué

  • 4
  • 1
Cet anticorp PDCD1 (Camrelizumab Biosimilar) est non-conjugé

Application

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

Classe de qualité

Research Grade
  • Expression System

    Mammalian cells

    Fonction

    Camrelizumab Biosimilar, PD-1 Monoclonal Antibody

    Attributs du produit

    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.

    Purification

    Protein A or G affinity column

    Pureté

    >95 % by reducing SDS-PAGE

    niveau d'endotoxine

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

    Immunogène

    Human PD1
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    > 3 mg/mL

    Stock

    4 °C,-20 °C

    Stockage commentaire

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

    PDCD1 (Camrelizumab Biosimilar)

    Autre désignation

    Camrelizumab Biosimilar

    Classe de substances

    Biosimilar
Vous êtes ici:
Chat with us!