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FGF17 antibody (AA 23-180)

This Rabbit Polyclonal antibody specifically detects FGF17 in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7267183

Quick Overview for FGF17 antibody (AA 23-180) (ABIN7267183)

Target

See all FGF17 Antibodies
FGF17 (Fibroblast Growth Factor 17 (FGF17))

Reactivity

  • 58
  • 7
  • 4
  • 2
  • 2
  • 1
  • 1
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  • 1
Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
  • 1
  • 1
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  • 1
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  • 1
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This FGF17 antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

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    AA 23-180

    Purpose

    FGF17 Rabbit pAb

    Sequence

    TQGENHPSPN FNQYVRDQGA MTDQLSRRQI REYQLYSRTS GKHVQVTGRR ISATAEDGNK FAKLIVETDT FGSRVRIKGA ESEKYICMNK RGKLIGKPSG KSKDCVFTEI VLENNYTAFQ NARHEGWFMA FTRQGRPRQA SRSRQNQREA HFIKRLYQ

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 23-180 of human FGF17 (NP_003858.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:1000,IF,1:50 - 1:200

    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

    FGF17 (Fibroblast Growth Factor 17 (FGF17))

    Alternative Name

    FGF17

    Background

    This gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants.,FGF17,FGF-13,FGF-17,HH20,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Growth factor,Cardiovascular,Angiogenesis,FGF17

    Molecular Weight

    23kDa/24kDa

    Gene ID

    8822

    UniProt

    O60258

    Pathways

    Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway
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