PDCD10 anticorps

N° du produit ABIN6989859

Détail du produit anti-PDCD10 anticorps

Antigène: PDCD10 (Programmed Cell Death 10 (PDCD10))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PDCD10 est non-conjugé

Application: 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

Information d'application

Indications d'application: WB 1:300-5000
IF()

Restrictions: For Research Use only

Stockage

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

Détails sur PDCD10

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:

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