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C9ORF91 antibody (AA 151-250) (Cy7)

C9ORF91 Reactivity: Human WB, IF (p), IF (cc) Host: Rabbit Polyclonal Cy7
Catalog No. ABIN1707625
  • Target See all C9ORF91 products
    C9ORF91 (Chromosome 9 Open Reading Frame 91 (C9ORF91))
    Binding Specificity
    • 14
    • 8
    • 7
    • 6
    AA 151-250
    Reactivity
    Human
    Host
    • 28
    Rabbit
    Clonality
    • 28
    Polyclonal
    Conjugate
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C9ORF91 antibody is conjugated to Cy7
    Application
    • 28
    • 15
    • 13
    • 13
    • 12
    • 12
    • 5
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
    Predicted Reactivity
    Human,Mouse,Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C9ORF91
    Isotype
    IgG
  • Application Notes
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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
    C9ORF91 (Chromosome 9 Open Reading Frame 91 (C9ORF91))
    Alternative Name
    C9orf91 (C9ORF91 Products)
    Synonyms
    RP11-402G3.2 antibody, transmembrane protein 268 antibody, TMEM268 antibody
    Background

    Synonyms: C9orf91, Chromosome 9 open reading frame 91, CI091_HUMAN, RP11-402G3.2, Transmembrane protein C9orf91.

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered 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. The C9orf91 gene product has been provisionally designated C9orf91 pending further characterization. There are three isoforms of C9orf91 that are produced as a result of alternative splicing events.

    Gene ID
    203197
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