×
Pour une meilleure utilisation, nous vous conseillons d’activer Javascript dans votre navigateur.
PDCD10 anticorps
PDCD10
Reactivité: Humain, Rat, Souris
IHC
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7009630
Détail du produit anti-PDCD10 anticorps
(cache)
Antigène
Voir toutes PDCD10 Anticorps
PDCD10
(Programmed Cell Death 10 (PDCD10))
Reactivité
Humain, Rat, Souris
Hôte
Toutes les hôtes sur PDCD10 Anticorps
Lapin
Clonalité
Toutes les clonalités sur PDCD10 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers PDCD10 Anticorps
Cet anticorp PDCD10 est non-conjugé
Application
Tous les applications à travers PDCD10 Anticorps.
Immunohistochemistry (IHC)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Recombinant fusion protein of human PDCD10 (NP_009148.2).
Isotype
IgG
Alternatives
(show)
Information d'application
(cache)
Indications d'application
IHC 1:50-1:200
Restrictions
For Research Use only
Stockage
(cache)
Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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.
Détails sur PDCD10
(cache)
Antigène
PDCD10
(Programmed Cell Death 10 (PDCD10))
Autre désignation
PDCD10 (PDCD10 Produits )
Synonymes
anticorps CCM3, anticorps TFAR15, anticorps 2410003B13Rik, anticorps Ccm3, anticorps Tfa15, anticorps Tfar15, anticorps zgc:85629, anticorps ccm3a, anticorps pdcd10, anticorps zgc:65826, anticorps programmed cell death 10, anticorps programmed cell death 10 S homeolog, anticorps programmed cell death 10b, anticorps programmed cell death 10a, anticorps PDCD10, anticorps Pdcd10, anticorps pdcd10.S, anticorps pdcd10b, anticorps pdcd10a
Sujet
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
Vus récemment
(cache)