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C15orf40 anticorps

Cet anticorps anti-C15orf40 est un anticorps Lapin Polyclonal détectant C15orf40 dans WB, ELISA et IHC. Adapté pour Humain.
N° du produit ABIN7246064

Aperçu rapide pour C15orf40 anticorps (ABIN7246064)

Antigène

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

Reactivité

  • 25
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 22
  • 3
Lapin

Clonalité

  • 22
  • 3
Polyclonal

Conjugué

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp C15orf40 est non-conjugé

Application

  • 13
  • 11
  • 9
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human C15orf40

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

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

    Autre désignation

    C15orf40

    Sujet

    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.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 16 kDa

    UniProt

    Q8WUR7
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