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MURF1 / IRF Antibody (Internal)

Goat Polyclonal Antibody

     
  • IHC - MURF1 / IRF Antibody (Internal) ALS11891
    Anti-TRIM63 / MURF1 antibody IHC of human skeletal muscle.
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
IHC-P, E
Primary Accession Q969Q1
Reactivity Human, Monkey
Host Goat
Clonality Polyclonal
Calculated MW 40kDa
Dilution ELISA (1:32000), IHC-P (1.25 µg/ml),
Additional Information
Gene ID 84676
Other Names E3 ubiquitin-protein ligase TRIM63, 6.3.2.-, Iris RING finger protein, Muscle-specific RING finger protein 1, MuRF-1, MuRF1, RING finger protein 28, Striated muscle RING zinc finger protein, Tripartite motif-containing protein 63, TRIM63, IRF, MURF1, RNF28, SMRZ
Target/Specificity Human TRIM63 / MURF1.
Reconstitution & Storage Store at -20°C. Minimize freezing and thawing.
PrecautionsMURF1 / IRF Antibody (Internal) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name TRIM63
Synonyms IRF, MURF1, RNF28, SMRZ
Function E3 ubiquitin ligase. Mediates the ubiquitination and subsequent proteasomal degradation of CKM, GMEB1 and HIBADH. Regulates the proteasomal degradation of muscle proteins under amino acid starvation, where muscle protein is catabolized to provide other organs with amino acids. Inhibits de novo skeletal muscle protein synthesis under amino acid starvation. Regulates proteasomal degradation of cardiac troponin I/TNNI3 and probably of other sarcomeric-associated proteins. May play a role in striated muscle atrophy and hypertrophy by regulating an anti-hypertrophic PKC-mediated signaling pathway. May regulate the organization of myofibrils through TTN in muscle cells.
Cellular Location Cytoplasm. Nucleus. Cytoplasm, myofibril, sarcomere, M line. Cytoplasm, myofibril, sarcomere, Z line Note=Colocalizes with TNNI3 in myocytes (By similarity). Localizes to the M- and Z-lines in skeletal muscle.
Tissue Location Muscle specific. Selectively expressed in heart and skeletal muscle. Also expressed in the iris
Research Areas
Citations (0)
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Background

E3 ubiquitin ligase. Mediates the ubiquitination and subsequent proteasomal degradation of CKM, GMEB1 and HIBADH. Regulates the proteasomal degradation of muscle proteins under amino acid starvation, where muscle protein is catabolized to provide other organs with amino acids. Inhibits de novo skeletal muscle protein synthesis under amino acid starvation. Regulates proteasomal degradation of cardiac troponin I/TNNI3 and probably of other sarcomeric-associated proteins. May play a role in striated muscle atrophy and hypertrophy by regulating an anti- hypertrophic PKC-mediated signaling pathway. May regulate the organization of myofibrils through TTN in muscle cells.

References

Centner T.,et al.J. Mol. Biol. 306:717-726(2001).
Wistow G.,et al.Mol. Vis. 8:185-195(2002).
Stanchi F.,et al.Submitted (MAR-2000) to the EMBL/GenBank/DDBJ databases.
Dai K.-S.,et al.J. Biol. Chem. 276:23992-23999(2001).
Ota T.,et al.Nat. Genet. 36:40-45(2004).

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Discontinued
Cat# ALS11891
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