POLR1D Polyclonal Antibody

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.

Research Area: Epigenetics and Nuclear Signaling

Synonyms:
AC19, DNA directed RNA polymerase I 16 kDa polypeptide, DNA directed RNA polymerase I subunit D, DNA directed RNA polymerases I and III subunit RPAC2, DNA-directed RNA polymerase I subunit D, DNA-directed RNA polymerases I and III subunit RPAC2, FLJ20616, hRPA19, MGC9850, POLR1C, POLR1D, Polymerase (RNA) I polypeptide D, Polymerase (RNA) I polypeptide D, 16kDa, RNA polymerase I 16 kDa subunit, RNA polymerases I and III subunit AC2, RPA16, RPA9, RPAC2, RPAC2, RPC16, RPO1 3

Immunogen: Fusion protein of human POLR1D

Swissprot: Q9Y2S0
Gene Accession: BC015319

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 0.84 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.