Recombinant IMP3 anticorps

N° du produit ABIN7881166

Cet anticorps anti-IMP3 Monoclonal Lapin (Clone IMP3-8934R) (ABIN7881166) détecte spécifiquement IMP3 dans IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Recombinant IMP3 anticorps (ABIN7881166)

Antigène: IMP3 (IMP3, U3 Small Nucleolar Ribonucleoprotein (IMP3))

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp IMP3 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: IMP3-8934R

Détail du produit anti-IMP3 anticorps

Fonction: IMP3 Antibody / Insulin like growth factor 2 mRNA binding protein 3

Purification: Protein A/G affinity

Immunogène: A recombinant fragment of human protein was used as the immunogen for the IMP3 antibody.

Isotype: IgG, kappa

Information d'application

Indications d'application: Optimal dilution of the IMP3 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

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: Aliquot the IMP3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur IMP3

Antigène: IMP3 (IMP3, U3 Small Nucleolar Ribonucleoprotein (IMP3))

Autre désignation: IMP3

Sujet: Imp3, also known as BRMS2, C15orf12 or MRPS4, is a 184 amino acid protein that contains one S4 RNA-binding domain and is the mammalian homolog of the yeast Imp3 protein. Localized to the nucleus, Imp3 exists as a component of a heterotrimeric complex consisting of MPP10, Imp3 and Imp4 and, in this complex, plays a key role in early cleavage events during pre-18S ribosomal processing. The gene encoding Imp3 maps to human chromosome 15, which houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

UniProt: Q9NV31