NPAP1 anticorps (AA 800-850) (Cy5)

N° du produit ABIN1421592

Cet anticorps anti-NPAP1 est un anticorps Lapin Polyclonal détectant NPAP1 dans WB et IF (p). Adapté pour Humain.

Aperçu rapide pour NPAP1 anticorps (AA 800-850) (Cy5) (ABIN1421592)

Antigène: NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NPAP1 est conjugé à/à la Cy5

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-NPAP1 anticorps (Cy5)

Épitope: AA 800-850

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human NPAP1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur NPAP1

Antigène: NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))

Autre désignation: NPAP1

Sujet:

Synonyms: NPAP1, NPAP 1, NPAP-1, Nuclear pore associated protein 1, NPAP1_HUMAN, C15orf2.

Background: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.

ID gène: 23742

UniProt: Q9NZP6