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C2CD2 antibody (FITC)

The Rabbit Polyclonal anti-C2CD2 antibody has been validated for WB and IF (p). It is suitable to detect C2CD2 in samples from Human, Mouse and Rat.
Catalog No. ABIN1405802

Quick Overview for C2CD2 antibody (FITC) (ABIN1405802)

Target

C2CD2 (C2 Calcium-Dependent Domain Containing 2 (C2CD2))

Reactivity

Human, Mouse, Rat

Host

  • 23
  • 2
Rabbit

Clonality

  • 25
Polyclonal

Conjugate

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C2CD2 antibody is conjugated to FITC

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 C2CD2/C21orf25

    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

    C2CD2 (C2 Calcium-Dependent Domain Containing 2 (C2CD2))

    Alternative Name

    C21orf25

    Background

    Synonyms: C2 calcium-dependent domain containing 2, C2 domain containing protein 2, C21orf25, C21orf258, C2CD2, Chromosome 21 open reading frame 25, MGC71445, TMEM24-like, TMEM24L, CU025_HUMAN.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C2CD2 is an 696 amino acid protien that is secreted. The C2CD2 gene product has been provisionally designated C2CD2 pending further characterization.

    Gene ID

    25966
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