POLR1D anticorps (AA 10-133)

N° du produit ABIN7599585

Cet anticorps anti-POLR1D Polyclonal Lapin (ABIN7599585) détecte spécifiquement POLR1D dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour POLR1D anticorps (AA 10-133) (ABIN7599585)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POLR1D est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-POLR1D anticorps

Épitope: AA 10-133

Fonction: Anti-POLR1D Antibody

Attributs du produit: Anti-POLR1D Antibody (ABIN7599585). Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human POLR1D recombinant protein (Position: K10-F133). Human POLR1D shares 90.3% amino acid (aa) sequence identity with mouse POLR1D.

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur POLR1D

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

Autre désignation: POLR1D

Sujet: DNA-ed RNA polymerases I and III subunit RPAC2 is a protein that in humans is encoded by the POLR1D gene. 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.

Poids moléculaire: 20 kDa

ID gène: 51082