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C14orf2 antibody

The Rabbit Polyclonal anti-C14orf2 antibody (ABIN7248335) specifically detects C14orf2 in ELISA, IHC and WB. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7248335
$538.80
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for C14orf2 antibody (ABIN7248335)

Target

C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))

Reactivity

  • 28
  • 10
  • 1
Human, Mouse

Host

  • 28
Rabbit

Clonality

  • 28
Polyclonal

Conjugate

  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This C14orf2 antibody is un-conjugated

Application

  • 13
  • 10
  • 9
  • 4
  • 1
ELISA, Immunohistochemistry (IHC), Western Blotting (WB)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human C14orf2

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:40-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.1 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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. Avoid freeze / thaw cycles.
  • Target

    C14orf2 (Chromosome 14 Open Reading Frame 2 (C14orf2))

    Alternative Name

    C14orf2

    Background

    C14orf2, also known as MP68, MP68 is a 58 amino acid mitochondrial protein that belongs to the small mitochondrial proteolipid family. The gene encoding MP68 maps to human chromosome 14, which houses over 700 genes and comprises nearly 3.5 % of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder α1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 7 kDa

    UniProt

    P56378
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