SNX29 anticorps

N° du produit ABIN7192586

L’anticorps Lapin Polyclonal anti-SNX29 a été validé pour IHC et ELISA. Il convient pour détecter SNX29 dans des échantillons de Humain.

Aperçu rapide pour SNX29 anticorps (ABIN7192586)

Antigène: SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SNX29 est non-conjugé

Application: Immunohistochemistry (IHC), ELISA

Détail du produit anti-SNX29 anticorps

Réactivité croisée: Humain, Souris

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of Human SNX29

Isotype: IgG

Information d'application

Indications d'application: ELISA:1:1000-1:2000, IHC:1:20-1:100,

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

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,-80 °C

Stockage commentaire: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Détails sur SNX29

Antigène: SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))

Autre désignation: SNX29

Sujet:

Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody

UniProt: Q8TEQ0