POLR1D anticorps

N° du produit ABIN7469578

L’anticorps Lapin Polyclonal anti-POLR1D a été validé pour WB et IHC (p). Il convient pour détecter POLR1D dans des échantillons de Humain.

Aperçu rapide pour POLR1D anticorps (ABIN7469578)

Antigène: POLR1D (Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POLR1D est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-POLR1D anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Full length human POLR1D (AAH00889) Recombinant protein.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: HepG2

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur POLR1D

Antigène: POLR1D (Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))

Autre désignation: POLR1D

Sujet:

Synonyms: RNA polymerase I and III subunit D , AC19 , POLR1C , RPA16 , RPA9 , RPAC2 , RPC16 , RPO1-3 , TCS2

Background: The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]

Poids moléculaire: 15 kDa

ID gène: 51082

UniProt: P0DPB6