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AB94981

Anti-EXOSC10/RRP6 antibody

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(3 Publications)

Rabbit Polyclonal EXOSC10/RRP6 antibody. Suitable for WB, IHC-P, IP and reacts with Human samples. Cited in 3 publications. Immunogen corresponding to Recombinant Fragment Protein within Human EXOSC10 aa 450 to C-terminus.

View Alternative Names

PMSCL, PMSCL2, RRP6, EXOSC10, Exosome complex component 10, Autoantigen PM/Scl 2, P100 polymyositis-scleroderma overlap syndrome-associated autoantigen, Polymyositis/scleroderma autoantigen 100 kDa, Polymyositis/scleroderma autoantigen 2, PM/Scl-100

4 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-EXOSC10/RRP6 antibody (AB94981)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-EXOSC10/RRP6 antibody (AB94981)

1/100 ab94981 staining EXOSC10/RRP6 in a paraffin-embedded Cal27 xenograft.

Immunoprecipitation - Anti-EXOSC10/RRP6 antibody (AB94981)
  • IP

Supplier Data

Immunoprecipitation - Anti-EXOSC10/RRP6 antibody (AB94981)

EXOSC10 antibody immunoprecipitates EXOSC 10 protein in IP experiments. Samples were separated by 7.5% SDS-PAGE. The immunoprecipitated EXOSC 10 protein was detected by EXOSC10 antibody diluted at 1/1000 dilution.

All lanes:

Immunoprecipitation - Anti-EXOSC10/RRP6 antibody (ab94981) at 2.5 µg

Lane 1:

293T whole cell extracts at 30 µg

Lane 2:

293T whole cell extracts with preimmune rabbit IgG control

Lane 3:

Immunoprecipitated 293T whole cell extracts using ab94981

Predicted band size: 101 kDa

false

Western blot - Anti-EXOSC10/RRP6 antibody (AB94981)
  • WB

Unknown

Western blot - Anti-EXOSC10/RRP6 antibody (AB94981)

7.5% SDS PAGE

All lanes:

Western blot - Anti-EXOSC10/RRP6 antibody (ab94981) at 1/3000 dilution

All lanes:

293T whole cell lysate at 30 µg

Predicted band size: 100 kDa

false

Western blot - Anti-EXOSC10/RRP6 antibody (AB94981)
  • WB

Supplier Data

Western blot - Anti-EXOSC10/RRP6 antibody (AB94981)

Samples were separated by 7.5% SDS-PAGE.

All lanes:

Western blot - Anti-EXOSC10/RRP6 antibody (ab94981) at 1/5000 dilution

Lane 1:

Non-transfected (–) 293T whole cell extracts at 30 µg

Lane 2:

EXOSC10 transfected (+) 293T whole cell extracts at 30 µg

Secondary

All lanes:

HRP-conjugated anti-rabbit IgG antibody

Predicted band size: 101 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

IHC-P, IP, WB

applications

Immunogen

Recombinant Fragment Protein within Human EXOSC10 aa 450 to C-terminus. The exact immunogen used to generate this antibody is proprietary information.

Q01780

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"}, "IP" : {"fullname" : "Immunoprecipitation", "shortname":"IP"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1/1000 - 1/10000", "WB-species-notes": "<p></p>", "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "1/100 - 1/1000", "IHCP-species-notes": "<p></p>", "IP-species-checked": "testedAndGuaranteed", "IP-species-dilution-info": "1/100 - 1/500", "IP-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7 Preservative: 0.01% Thimerosal (merthiolate) Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

EXOSC10 also known as RRP6 is an important component of the RNA exosome complex which plays a role in RNA processing and degradation. This protein is approximately 97 kDa in mass. It is localized mainly in the nucleus with a high expression level in nucleoli. The EXOSC10 protein contributes to the catalytic core of the exosome allowing it to perform 3’ to 5’ exonuclease activity on a variety of RNA substrates.
Biological function summary

Beyond its activity as an exonuclease EXOSC10 participates in the degradation of aberrant RNA molecules and the maturation of stable RNA species like rRNA. As a member of the RNA exosome complex it functions alongside other core exosome components to maintain RNA homeostasis. This assembly is essential for the surveillance and decay of faulty RNA regulatory RNA and the normal turnover of cellular RNA. The process ensures fidelity in gene expression and the prevention of toxic RNA accumulation.

Pathways

EXOSC10 plays a significant role in RNA processing pathways that involve RNA surveillance and degradation mechanisms. It acts in coordination with other proteins such as DIS3 and EXOSC5 in these pathways to ensure the correct maturation and quality control of RNA. The RNA exosome including EXOSC10 intersects with the nonsense-mediated decay pathway a cellular mechanism that identifies and degrades mRNAs containing premature stop codons therefore preventing potential truncated protein production.

Defects in EXOSC10 have been linked to diseases such as various forms of cancer and autoimmunity. The malfunction of EXOSC10 can disrupt RNA processing and degradation leading to the accumulation of defective RNAs and misregulated gene expression contributing to oncogenesis. In autoimmune conditions abnormal RNA processing by EXOSC10 may lead to altered immune responses. Associations with RPL5 and other ribosomal proteins have also been noted in the context of these disorders highlighting the importance of EXOSC10 in maintaining cellular RNA balance and integrity.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

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 (PubMed : 34516797). 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. EXOSC10 is required for nucleolar localization of C1D and probably mediates the association of MTREX, C1D and MPHOSPH6 with the RNA exosome involved in the maturation of 5.8S rRNA. Plays a role in the recruitment of replication protein A complex (RPA) and RAD51 to DNA double-strand breaks caused by irradiation, contributing to DNA repair by homologous recombination (PubMed : 25632158, PubMed : 31086179). Regulates levels of damage-induced RNAs in order to prevent DNA-RNA hybrid formation at DNA double-strand breaks and limit DNA end resection after damage (PubMed : 31086179). Plays a role in oocyte development, maturation and survival (By similarity). Required for normal testis development and mitotic division of spermatogonia (By similarity). Plays a role in proper embryo development (By similarity). Required for global protein translation (PubMed : 26857222, PubMed : 36912080). Required for cell proliferation (PubMed : 36912080). Regulates metabolism of C9orf72-derived repeat RNA that can be translated into toxic dipeptide repeat proteins (PubMed : 32830871).
See full target information EXOSC10

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

Cancer gene therapy 30:149-162 PubMed36123390

2022

YAP 5-methylcytosine modification increases its mRNA stability and promotes the transcription of exosome secretion-related genes in lung adenocarcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Wenjun Yu,Congcong Zhang,Yikun Wang,Xiaoting Tian,Yayou Miao,Fanyu Meng,Lifang Ma,Xiao Zhang,Jinjing Xia

Redox biology 38:101801 PubMed33232910

2020

The mA reader YTHDC2 inhibits lung adenocarcinoma tumorigenesis by suppressing SLC7A11-dependent antioxidant function.

Applications

Unspecified application

Species

Unspecified reactive species

Lifang Ma,Tianxiang Chen,Xiao Zhang,Yayou Miao,Xiaoting Tian,Keke Yu,Xin Xu,Yongjie Niu,Susu Guo,Congcong Zhang,Shiyu Qiu,Yongxia Qiao,Wentao Fang,Lutao Du,Yongchun Yu,Jiayi Wang

Nucleic acids research 44:2873-87 PubMed26809675

2016

Identification of factors involved in target RNA-directed microRNA degradation.

Applications

WB

Species

Human

Gabrielle Haas,Semih Cetin,Mélanie Messmer,Béatrice Chane-Woon-Ming,Olivier Terenzi,Johana Chicher,Lauriane Kuhn,Philippe Hammann,Sébastien Pfeffer
View all publications

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