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PDCD10 anticorps (AA 1-212)

Cet anticorps anti-PDCD10 est un anticorps Lapin Polyclonal détectant PDCD10 dans ELISA et WB. Adapté pour Humain, Rat et Souris.
N° du produit ABIN6654194

Aperçu rapide pour PDCD10 anticorps (AA 1-212) (ABIN6654194)

Antigène

Voir toutes PDCD10 Anticorps
PDCD10 (Programmed Cell Death 10 (PDCD10))

Reactivité

Humain, Rat, Souris

Hôte

  • 55
  • 2
Lapin

Clonalité

  • 55
  • 2
Polyclonal

Conjugué

  • 17
  • 6
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PDCD10 est non-conjugé

Application

  • 24
  • 18
  • 13
  • 13
  • 5
  • 5
  • 3
  • 3
  • 2
  • 1
ELISA, Western Blotting (WB)
  • Épitope

    • 15
    • 10
    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-212

    Purification

    Antigen affinity purified

    Immunogène

    Human PDCD10 recombinant protein (amino acids M1-A212) was used as the immunogen for the PDCD10 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the PDCD10 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,Direct ELISA: 0.1-0.5 μg/mL (human recombinant protein)

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the PDCD10 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    Autre désignation

    PDCD10

    Sujet

    Programmed cell death protein 10 is a protein that in humans is encoded by the PDCD10 gene. This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    UniProt

    Q9BUL8
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