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C8ORF37 antibody (AA 1-100) (HRP)

This Rabbit Polyclonal antibody specifically detects C8ORF37 in WB, ELISA, IHC (fro) and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN1710955

Quick Overview for C8ORF37 antibody (AA 1-100) (HRP) (ABIN1710955)

Target

See all C8ORF37 Antibodies
C8ORF37 (Chromosome 8 Open Reading Frame 37 (C8ORF37))

Reactivity

Human

Host

  • 14
Rabbit

Clonality

  • 14
Polyclonal

Conjugate

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  • 1
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This C8ORF37 antibody is conjugated to HRP

Application

  • 14
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  • 13
  • 2
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Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    AA 1-100

    Predicted Reactivity

    Human

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C8orf37

    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

    C8ORF37 (Chromosome 8 Open Reading Frame 37 (C8ORF37))

    Alternative Name

    C8orf37

    Background

    Synonyms: C8orf37, CH037_HUMAN, Uncharacterized protein C8orf37.

    Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf37 gene product has been provisionally designated C8orf37 pending further characterization.

    Gene ID

    157657
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