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C9ORF173 antibody (AbBy Fluor® 750)

The Rabbit Polyclonal anti-C9ORF173 antibody has been validated for WB. It is suitable to detect C9ORF173 in samples from Human, Mouse and Rat.
Catalog No. ABIN4998784

Quick Overview for C9ORF173 antibody (AbBy Fluor® 750) (ABIN4998784)

Target

C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))

Reactivity

Human, Mouse, Rat

Host

  • 16
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C9ORF173 antibody is conjugated to AbBy Fluor® 750

Application

  • 16
  • 3
Western Blotting (WB)
  • Cross-Reactivity

    Mouse

    Predicted Reactivity

    Human,Rat,Dog

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C9orf173

    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.

    Storage

    -20 °C

    Storage Comment

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

    Expiry Date

    12 months
  • Target

    C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))

    Alternative Name

    C9orf173

    Background

    Synonyms: C9orf173, Chromosome 9 open reading frame 173, CI173_HUMAN, Uncharacterized protein C9orf173.

    Background: C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    Gene ID

    441476
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