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PDCD10 anticorps

Cet anticorps anti-PDCD10 est un anticorps Lapin Polyclonal détectant PDCD10 dans WB et IF. Adapté pour Humain et Souris.
N° du produit ABIN6989859

Aperçu rapide pour PDCD10 anticorps (ABIN6989859)

Antigène

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

Reactivité

  • 40
  • 27
  • 12
Humain, Souris

Hôte

  • 53
  • 2
Lapin

Clonalité

  • 53
  • 2
Polyclonal

Conjugué

  • 17
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PDCD10 est non-conjugé

Application

  • 20
  • 19
  • 13
  • 13
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  •  Réactivité croisée

    Humain, Souris

    Purification

    Purified by Protein A.

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-212 of human PDCD10 (NP_009148.2).

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    IF()

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C for 12 months.

    Date de péremption

    12 months
  • Antigène

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    Autre désignation

    PDCD10

    Sujet

    Synonyms: PDCD10,CCM3,TFAR15

    Background: 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.

    ID gène

    11235

    UniProt

    Q9BUL8
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