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ELK Biotechnology
SKU(재고 관리 코드):ES9612
RPAC2 rabbit pAb
RPAC2 rabbit pAb
Applications: WB;ELISA
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1:500-2000 ELISA 1:5000-20000
Immunogen: Synthesized peptide derived from part region of human protein
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Observed_band(KD): 14kD
Human_gene_id: 51082
Human_swiss_prot_no: Q9Y2S0
Subcellular_location: nucleoplasm,DNA-directed RNA polymerase III complex,DNA-directed RNA polymerase I complex,cytosol,
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],
Reactivity: Human;Rat;Mouse;
Source: Rabbit
Dilution: WB 1:500-2000 ELISA 1:5000-20000
Immunogen: Synthesized peptide derived from part region of human protein
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Observed_band(KD): 14kD
Human_gene_id: 51082
Human_swiss_prot_no: Q9Y2S0
Subcellular_location: nucleoplasm,DNA-directed RNA polymerase III complex,DNA-directed RNA polymerase I complex,cytosol,
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],
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