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LIFR antibody (AA 500-700)

The Rabbit Polyclonal anti-LIFR antibody has been validated for WB. It is suitable to detect LIFR in samples from Human.
Catalog No. ABIN6143204

Quick Overview for LIFR antibody (AA 500-700) (ABIN6143204)

Target

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

Reactivity

  • 43
  • 18
  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 65
  • 7
Rabbit

Clonality

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Polyclonal

Conjugate

  • 38
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  • 8
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This LIFR antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

    • 6
    • 4
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    • 4
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    • 4
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    • 3
    • 3
    • 2
    • 2
    • 1
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    • 1
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    • 1
    AA 500-700

    Sequence

    NPYTLYTFRI RCSTETFWKW SKWSNKKQHL TTEASPSKGP DTWREWSSDG KNLIIYWKPL PINEANGKIL SYNVSCSSDE ETQSLSEIPD PQHKAEIRLD KNDYIISVVA KNSVGSSPPS KIASMEIPND DLKIEQVVGM GKGILLTWHY DPNMTCDYVI KWCNSSRSEP CLMDWRKVPS NSTETVIESD EFRPGIRYNF F

    Cross-Reactivity

    Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 500-700 of human LIFR (NP_002301.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    LIFR (Leukemia Inhibitory Factor Receptor alpha (LIFR))

    Alternative Name

    LIFR

    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 the same protein have been found for this gene.,LIFR,CD118,LIF-R,SJS2,STWS,SWS,Cell Biology & Developmental Biology,Immunology & Inflammation,CD markers,Cytokines,Cell Intrinsic Innate Immunity Signaling Pathway,Stem Cells,Embryonic Stem Cells,LIFR

    Molecular Weight

    123 kDa

    Gene ID

    3977

    UniProt

    P42702

    Pathways

    JAK-STAT Signaling, Growth Factor Binding
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