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C15orf40 antibody

The Rabbit Polyclonal anti-C15orf40 antibody (ABIN7246064) specifically detects C15orf40 in ELISA, WB and IHC. The antibody is reactive with Human samples.
Catalog No. ABIN7246064
$538.80
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for C15orf40 antibody (ABIN7246064)

Target

C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Reactivity

  • 30
  • 10
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 27
  • 3
Rabbit

Clonality

  • 27
  • 3
Polyclonal

Conjugate

  • 12
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C15orf40 antibody is un-conjugated

Application

  • 14
  • 14
  • 10
  • 2
  • 1
  • 1
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human C15orf40

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 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

    C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

    Alternative Name

    C15orf40

    Background

    Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.

    Molecular Weight

    Observed_MW: Refer to figures

    Calculated_MW: 16 kDa

    UniProt

    Q8WUR7
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