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FGFR1 anticorps (AA 489-520)

Cet anticorps anti-FGFR1 est un anticorps Lapin Polyclonal détectant FGFR1 dans WB. Adapté pour Humain.
N° du produit ABIN5647574

Aperçu rapide pour FGFR1 anticorps (AA 489-520) (ABIN5647574)

Antigène

Voir toutes FGFR1 Anticorps
FGFR1 (Fibroblast Growth Factor Receptor 1 (FGFR1))

Reactivité

  • 228
  • 98
  • 94
  • 23
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  • 15
  • 7
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  • 2
  • 2
  • 1
Humain

Hôte

  • 221
  • 42
  • 1
Lapin

Clonalité

  • 211
  • 53
Polyclonal

Conjugué

  • 126
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  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
Cet anticorp FGFR1 est non-conjugé

Application

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Western Blotting (WB)
  • Épitope

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    • 1
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    AA 489-520

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids 489-520 (FGQVVLAEAIGLDKDKPNRVTKVAVKMLKSDA-human) were used as the immunogen for the FGFR1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the FGFR1 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the FGFR1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    FGFR1 (Fibroblast Growth Factor Receptor 1 (FGFR1))

    Autre désignation

    FGFR1 / Fibroblast growth factor receptor 1

    Sujet

    FGFR1, Fibroblast growth factor receptor 1, also known as basic fibroblast growth factor receptor 1, fms-related tyrosine kinase-2 / Pfeiffer syndrome, and CD331, is a receptor tyrosine kinase whose ligands are specific members of the fibroblast growth factor family. The FGFR1 gene is localized to 8p12-p11.2 by in situ hybridization. FGFR1 is essential for the normal formation of the organ of Corti and that phenotype severity observed in FGFR1 mutants is dependent on the dose of FGFR1. Mutations in this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, squamous cell lung cancer and autosomal dominant Kallmann syndrome 2.

    UniProt

    P11362

    Pathways

    Signalisation RTK, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Sensory Perception of Sound, Stem Cell Maintenance, S100 Proteins
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