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Anti-Human EXOSC10 Polyclonal Antibody (HX842014)

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Aperçu
Numéro de catalogueHX842014
Description
Anti-Human EXOSC10 Polyclonal Antibody (HX842014) is a rabbit polyclonal antibody detecting EXOSC10 in ELISA, IHC, WB. Suitable for Human, Mouse, Rat.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
  • ●Multi-Species — Cross-reactive for translational research.
Reactivité des espècesHuman, Mouse, Rat
ApplicationsELISA, IHC, WB
Espèce hôteRabbit
ClonalitéPolyclonal
IsotypeIgG
Immunogène E. coli - derived recombinant Human EXOSC10 (Thr286-Lys479).
Cible PMSCL2, EXOSC10, Exosome component 10, P100 polymyositis-scleroderma overlap syndrome-associated autoantigen, PM/Scl-100, Autoantigen PM/Scl 2, PMSCL, Polymyositis/scleroderma autoantigen 100 kDa, Polymyositis/scleroderma autoantigen 2, RRP6
Purification Purified by antigen affinity column.
Numéro d'accès Q01780
Forme Liquid
Tampon de stockage 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Reférez-vous aux informations spécifiques sur le tampon dans la copie papier du datasheet ou dans le COA spécifique au lot.

Informations d'utilisation du produit
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stabilité et stockage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Contexte

Exosome complex component 10 (EXOSC10) is a ~100 kDa protein. 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. Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome. 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.

1. Singh, S. et al. (2021) Science (New York, N.Y.) 373, eabj5338. PMID: 34516797
2. Marin-Vicente, C. et al. (2015) Journal of cell science 128, 1097-107. PMID: 25632158
3. Domingo-Prim, J. et al. (2019) Nature communications 10, 2135. PMID: 31086179
4. Knight, JR. et al. (2016) RNA (New York, N.Y.) 22, 623-35. PMID: 26857222
5. Chen, Y. et al. (2023) Nucleic acids research 51, 3934-3949. PMID: 36912080
6. Kawabe, Y. et al. (2020) The EMBO journal 39, e102700. PMID: 32830871
Note For research use only.
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Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
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C₂ (Working Conc.)
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