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C18orf8 antibody (AbBy Fluor® 750)

This anti-C18orf8 antibody is a Rabbit Polyclonal antibody detecting C18orf8 in WB and IF (p). Suitable for Human.
Catalog No. ABIN5006843

Quick Overview for C18orf8 antibody (AbBy Fluor® 750) (ABIN5006843)

Target

See all C18orf8 Antibodies
C18orf8 (Chromosome 18 Open Reading Frame 8 (C18orf8))

Reactivity

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  • 1
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Human

Host

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Rabbit

Clonality

  • 35
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Polyclonal

Conjugate

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  • 1
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  • 1
  • 1
  • 1
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This C18orf8 antibody is conjugated to AbBy Fluor® 750

Application

  • 30
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Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Cross-Reactivity

    Human

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human MIC1/C18orf8

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    C18orf8 (Chromosome 18 Open Reading Frame 8 (C18orf8))

    Alternative Name

    MIC1

    Background

    Synonyms: C18orf8, Chromosome 18 open reading frame 8, Colon cancer associated protein Mic1, Colon cancer-associated protein Mic1, HsT2591, Mic-1, MIC1, MIC1_HUMAN, Uncharacterized protein C18orf8.

    Background: MIC1 is a 657 amino acid protein that contains one MIC1 domain and is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

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