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C2ORF44 antibody (PE)

This anti-C2ORF44 antibody is a Rabbit Polyclonal antibody detecting C2ORF44 in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN2171421

Quick Overview for C2ORF44 antibody (PE) (ABIN2171421)

Target

C2ORF44 (Chromosome 2 Open Reading Frame 44 (C2ORF44))

Reactivity

  • 20
  • 16
  • 16
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 20
Rabbit

Clonality

  • 20
Polyclonal

Conjugate

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C2ORF44 antibody is conjugated to PE

Application

  • 19
  • 13
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C2orf44

    Isotype

    IgG
  • Application Notes

    FCM: (1:20-100)
    Optimal working dilution should be determined by the investigator.

    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

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: 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.
  • Target

    C2ORF44 (Chromosome 2 Open Reading Frame 44 (C2ORF44))

    Alternative Name

    C2orf44

    Background

    Synonyms: C2orf44, CB044_HUMAN, Chromosome 2 open reading frame 44, FLJ21945, PP384, WD repeat-containing protein C2orf44.

    Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf44 gene product has been provisionally designated C2orf44 pending further characterization.

    Gene ID

    80304
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