Mouse Monoclonal EXOSC9 antibody. Suitable for WB and reacts with Recombinant fragment samples. Immunogen corresponding to Recombinant Fragment Protein within Human EXOSC9.
pH: 7.4
Preservative: 0.05% Sodium azide
Constituents: 1% BSA, 0.812% Sodium chloride, 0.1312% Sodium phosphate, 0.1136% Disodium hydrogenorthophosphate, 0.03% Tripotassium orthophosphate, 0.0225% Potassium chloride, 0.0204% Potassium phosphate monobasic
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Recombinant fragment | Tested |
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Species Recombinant fragment | Dilution info - | Notes - |
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Non-catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. In the nucleus, the RNA exosome complex is involved in proper maturation of stable RNA species such as rRNA, snRNA and snoRNA, in the elimination of RNA processing by-products and non-coding 'pervasive' transcripts, such as antisense RNA species and promoter-upstream transcripts (PROMPTs), and of mRNAs with processing defects, thereby limiting or excluding their export to the cytoplasm. The RNA exosome may be involved in Ig class switch recombination (CSR) and/or Ig variable region somatic hypermutation (SHM) by targeting AICDA deamination activity to transcribed dsDNA substrates. In the cytoplasm, the RNA exosome complex is involved in general mRNA turnover and specifically degrades inherently unstable mRNAs containing AU-rich elements (AREs) within their 3' untranslated regions, and in RNA surveillance pathways, preventing translation of aberrant mRNAs. It seems to be involved in degradation of histone mRNA. The catalytic inactive RNA exosome core complex of 9 subunits (Exo-9) is proposed to play a pivotal role in the binding and presentation of RNA for ribonucleolysis, and to serve as a scaffold for the association with catalytic subunits and accessory proteins or complexes. EXOSC9 binds to ARE-containing RNAs.
PMSCL1, EXOSC9, Exosome complex component RRP45, Autoantigen PM/Scl 1, Exosome component 9, P75 polymyositis-scleroderma overlap syndrome-associated autoantigen, Polymyositis/scleroderma autoantigen 1, Polymyositis/scleroderma autoantigen 75 kDa, PM/Scl-75
Mouse Monoclonal EXOSC9 antibody. Suitable for WB and reacts with Recombinant fragment samples. Immunogen corresponding to Recombinant Fragment Protein within Human EXOSC9.
pH: 7.4
Preservative: 0.05% Sodium azide
Constituents: 1% BSA, 0.812% Sodium chloride, 0.1312% Sodium phosphate, 0.1136% Disodium hydrogenorthophosphate, 0.03% Tripotassium orthophosphate, 0.0225% Potassium chloride, 0.0204% Potassium phosphate monobasic
ab54283 was purified using protein G column chromatography from culture supernatant of hybridoma cultured in a medium containing bovine IgG-depleted (approximately 95%) fetal bovine serum. Filtered through a 0.22 µm membrane.
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EXOSC9 also known as Exosome Component 9 or 3'-5' exoribonuclease CSL4 plays an important mechanical role in RNA processing and degradation. This protein is a component of the exosome complex which is responsible for the controlled breakdown of RNA molecules. The mass of EXOSC9 is approximately 45 kDa. It is expressed in a variety of tissues including brain liver and heart highlighting its importance in diverse cellular activities.
EXOSC9 functions as a critical element in RNA surveillance and decay pathways within cells. It is a core component of the RNA exosome complex which consists of multiple proteins working together to process and degrade various types of RNA such as rRNA mRNA and small RNAs. The exosome complex plays a significant role in maintaining RNA stability and quality control within eukaryotic cells ensuring the accurate regulation of gene expression.
EXOSC9 participates in essential processes involving RNA processing and decay. It is a part of the RNA decay pathway which is vital for the degradation of defective RNA molecules therefore preventing potential cellular dysfunction. EXOSC9 also interacts with proteins like EXOSC10 and EXOSC2 working collectively within the exosome complex to achieve its functionalities in these pathways. This interaction underlines its participation in the larger context of gene expression regulation.
Improper functioning of EXOSC9 has been linked to neurodegenerative conditions such as pontocerebellar hypoplasia. Such conditions result from defects in RNA processing and degradation leading to cellular dysregulation. EXOSC9 is also connected to specific cardiovascular disorders due to its involvement in RNA metabolism and stability. Additionally its interaction with other exosome components like EXOSC8 and EXOSC3 further connects it to broader pathways involved in these diseases.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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The molecular weight of the band on the western blot does not correspond to the molecular weight of the natural protein because only a fragment of the protein was used.
All lanes: Western blot - Anti-EXOSC9 antibody [2337C3a] (ab54283)
All lanes: Recombinant immunising protein
Predicted band size: 49 kDa
Observed band size: 42 kDa
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