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LIFR antibody (AA 22-441)

The Mouse Monoclonal anti-LIFR antibody has been validated for ELISA and FACS. It is suitable to detect LIFR in samples from Human.
Catalog No. ABIN7193531

Quick Overview for LIFR antibody (AA 22-441) (ABIN7193531)

Target

See all LIFR Antibodies
LIFR (Leukemia Inhibitory Factor Receptor alpha (LIFR))

Reactivity

  • 40
  • 14
  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 55
  • 6
Mouse

Clonality

  • 56
  • 5
Monoclonal

Conjugate

  • 30
  • 15
  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LIFR antibody is un-conjugated

Application

  • 48
  • 22
  • 17
  • 13
  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
ELISA, Flow Cytometry (FACS)

Clone

5D3G12
  • Binding Specificity

    • 6
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 22-441

    Purpose

    CD118 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human PLA2G7 (AA: 22-441) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    LIFR (Leukemia Inhibitory Factor Receptor alpha (LIFR))

    Alternative Name

    CD118

    Background

    This gene encodes a protein that belongs to the type I cytokine receptor family. This protein combines with a high-affinity converter subunit, gp130, to form a receptor complex that mediates the action of the leukemia inhibitory factor, a polyfunctional cytokine that is involved in cellular differentiation, proliferation and survival in the adult and the embryo. Mutations in this gene cause Schwartz-Jampel syndrome type 2, a disease belonging to the group of the bent-bone dysplasias. A translocation that involves the promoter of this gene, t(5,8)(p13,q12) with the pleiomorphic adenoma gene 1, is associated with salivary gland pleiomorphic adenoma, a common type of benign epithelial tumor of the salivary gland. Multiple splice variants encoding two different isoforms have been found for this gene.

    Molecular Weight

    123.7 kDa

    Gene ID

    3977

    UniProt

    P42702

    Pathways

    JAK-STAT Signaling, Growth Factor Binding
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