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FGFR1OP antibody

The Rabbit Polyclonal anti-FGFR1OP antibody has been validated for WB, IHC and ELISA. It is suitable to detect FGFR1OP in samples from Human and Mouse.
Catalog No. ABIN7241330

Quick Overview for FGFR1OP antibody (ABIN7241330)

Target

See all FGFR1OP Antibodies
FGFR1OP (FGFR1 Oncogene Partner (FGFR1OP))

Reactivity

  • 62
  • 19
  • 17
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 58
  • 4
  • 2
Rabbit

Clonality

  • 58
  • 6
Polyclonal

Conjugate

  • 29
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FGFR1OP antibody is un-conjugated

Application

  • 55
  • 26
  • 26
  • 12
  • 10
  • 9
  • 8
  • 6
  • 6
  • 3
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human FGFR1OP

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.7 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    FGFR1OP (FGFR1 Oncogene Partner (FGFR1OP))

    Alternative Name

    FGFR1OP

    Background

    This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6,8)(q27,p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. Alterations in this gene may also be associated with Crohn's disease, Graves' disease, and vitiligo. Alternatively spliced transcript variants that encode different proteins have been identified.

    Molecular Weight

    43 kDa

    UniProt

    O95684

    Pathways

    M Phase, Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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