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ZC2HC1C antibody (AbBy Fluor® 488)

This Rabbit Polyclonal antibody specifically detects ZC2HC1C in WB and IF (p). It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN1403656

Quick Overview for ZC2HC1C antibody (AbBy Fluor® 488) (ABIN1403656)

Target

ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))

Reactivity

  • 18
  • 17
  • 16
  • 2
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 18
Rabbit

Clonality

  • 18
Polyclonal

Conjugate

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ZC2HC1C antibody is conjugated to AbBy Fluor® 488

Application

  • 18
  • 12
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C14ORF140/FAM164C

    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.

    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

    ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))

    Alternative Name

    C14ORF140

    Background

    Synonyms: chromosome 14 open reading frame 140, FAM164C, family with sequence similarity 164 member C, FLJ23093, UPF0418 protein FAM164C, ZC21C_HUMAN.

    Background: Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5 % of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14,19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.

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