biological source
rat
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
5G8, monoclonal
species reactivity
mouse
technique(s)
immunoprecipitation (IP): suitable, western blot: suitable
isotype
IgG1κ
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Gene Information
mouse ... Eri1(67276)
General description
The protein named 3’-5’ exoribonuclease 1 or 3′-5′ exonuclease ERI1, Eri-1 homolog, Histone mRNA 3′-end-specific exoribonuclease, Histone mRNA 3′-exonuclease 1, or Protein 3′hExo (HEXO), and encoded by the human gene ERI1/ 3’EXO,/THEX1 is an RNA exonuclease that binds to the 3′-end of histone mRNAs and degrades them, suggesting that it plays an essential role in histone mRNA decay after replication. Eri1 also can degrade 3’ overhangs on short interfering RNAs (siRNAs) suggestion a possible wider role in RNA interference, and finally Eri1 also processes other RNAs, including ribosomal RNAs and Eri1 is part of a pre-mRNA processing complex and can bind ribosomal subunits and assembled ribosomes too. Recent research also has identified Eri1 as a regulator of micro RNA and plays a role in miRNA homeostasis, lymphocyte development and antiviral functions. Eri1 is localized to the cytoplasm and nucleus, as well as, the nucleolus in normal cells.
~40 kDa observed
Immunogen
Recombinant protein corresponding to mouse Eri1/Exoribonuclease 1.
Application
Research Category
Epigenetics & Nuclear Function
Epigenetics & Nuclear Function
Research Sub Category
RNA Metabolism & Binding Proteins
RNA Metabolism & Binding Proteins
This Anti-Eri1/Exoribonuclease 1 Antibody, clone 5G8 is validated for use in western blotting & IP for the detection of Eri1/Exoribonuclease 1.
Western Blotting Analysis: 0.5 µg/mL from a representative lot detected Eri1/Exoribonuclease 1 in 10 µg of mouse testis tissue lysate.
Western Blotting Analysis: A representative lot from an independent laboratory detected Eri1/Exoribonuclease 1 in MEF cell lysate (Hoefig, K. P., et al. (2012). Nat Struct Mol Biol. 20(1):73-81.).
Immunoprecipitation Analysis: A representative lot from an independent laboratory immunoprecipitated Eri1/Exoribonuclease 1 from MEF cell lysate (Hoefig, K. P., et al. (2012). Nat Struct Mol Biol. 20(1):73-81.).
Western Blotting Analysis: A representative lot from an independent laboratory detected Eri1/Exoribonuclease 1 in MEF cell lysate (Hoefig, K. P., et al. (2012). Nat Struct Mol Biol. 20(1):73-81.).
Immunoprecipitation Analysis: A representative lot from an independent laboratory immunoprecipitated Eri1/Exoribonuclease 1 from MEF cell lysate (Hoefig, K. P., et al. (2012). Nat Struct Mol Biol. 20(1):73-81.).
Physical form
Format: Purified
Protein G Purified
Purified rat monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Preparation Note
Stable for 1 year at 2-8°C from date of receipt.
Analysis Note
Evaluated by Western Blotting in NIH/3T3 cell lysate.
Western Blotting Analysis: 0.5 µg/mL of this antibody detected Eri1/Exoribonuclease 1 in 10 µg of NIH/3T3 cell lysate.
Western Blotting Analysis: 0.5 µg/mL of this antibody detected Eri1/Exoribonuclease 1 in 10 µg of NIH/3T3 cell lysate.
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Marion Declercq et al.
Nucleic acids research, 48(18), 10428-10440 (2020-09-23)
Cellular exonucleases involved in the processes that regulate RNA stability and quality control have been shown to restrict or to promote the multiplication cycle of numerous RNA viruses. Influenza A viruses are major human pathogens that are responsible for seasonal
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