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C6ORF132 antibody (AA 1001-1188) (HRP)

The Rabbit Polyclonal anti-C6ORF132 antibody has been validated for WB, ELISA, IHC (fro) and IHC (p). It is suitable to detect C6ORF132 in samples from Human.
Catalog No. ABIN1711859

Quick Overview for C6ORF132 antibody (AA 1001-1188) (HRP) (ABIN1711859)

Target

C6ORF132 (Chromosome 6 Open Reading Frame 132 (C6ORF132))

Reactivity

Human

Host

  • 14
Rabbit

Clonality

  • 14
Polyclonal

Conjugate

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This C6ORF132 antibody is conjugated to HRP

Application

  • 14
  • 13
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Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    AA 1001-1188

    Cross-Reactivity

    Human

    Predicted Reactivity

    Mouse,Rat,Cow,Sheep,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C6orf132

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    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.

    Handling Advice

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    Storage

    -20 °C

    Storage Comment

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

    Expiry Date

    12 months
  • Target

    C6ORF132 (Chromosome 6 Open Reading Frame 132 (C6ORF132))

    Alternative Name

    C6orf132

    Background

    Synonyms: bA7K24.2, C6orf132, CF132_HUMAN, Chromosome 6 open reading frame 132, Uncharacterized protein C6orf132.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf132 gene product has been provisionally designated C6orf132 pending further characterization.

    Gene ID

    647024
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