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WWOX antibody (AA 1-120)

The Rabbit Polyclonal anti-WWOX antibody has been validated for WB and IF. It is suitable to detect WWOX in samples from Human.
Catalog No. ABIN6150272

Quick Overview for WWOX antibody (AA 1-120) (ABIN6150272)

Target

See all WWOX Antibodies
WWOX (WW Domain Containing Oxidoreductase (WWOX))

Reactivity

  • 58
  • 42
  • 12
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 2
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  • 1
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This WWOX antibody is un-conjugated

Application

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

    • 12
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    • 2
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    AA 1-120

    Sequence

    MAALRYAGLD DTDSEDELPP GWEERTTKDG WVYYANHTEE KTQWEHPKTG KRKRVAGDLP YGWEQETDEN GQVFFVDHIN KRTTYLDPRL AFTVDDNPTK PTTRQRYDGS TTAMEILQGR

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-120 of human WWOX (NP_057457.1).

    Isotype

    IgG
  • Application Notes

    WB,1:1000 - 1:2000,IF,1:50 - 1:200

    Comment

    HIGH QUALITY

    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

    WWOX (WW Domain Containing Oxidoreductase (WWOX))

    Alternative Name

    WWOX

    Background

    This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants.,WWOX,D16S432E,EIEE28,FOR,FRA16D,HHCMA56,PRO0128,SCAR12,SDR41C1,WOX1,Epigenetics & Nuclear Signaling,Cancer,Tumor suppressors,p53 pathway,Cell Biology & Developmental Biology,Apoptosis,Growth factor,TNF,Neuroscience,Neurodegenerative Diseases,Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimer's Disease,WWOX

    Molecular Weight

    4 kDa/21 kDa/23 kDa/26 kDa/35 kDa/41 kDa/46 kDa

    Gene ID

    51741

    UniProt

    Q9NZC7
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