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Catalogue Number 151842
Applications IP WB
Antigen/Gene or Protein Targets Senataxin
Reactivity Human
Relevance Defects in Senataxin are the cause of neurodegenerative diseases AOA-2 and ALS4. Senataxin play vital roles in DNA repair and transcription termination. The staining pattern of the antibody is located in the nucleus and chromatin.
Host Rabbit
Immunogen A mixture of four peptides corresponding to the following amino acid ranges of human Senataxin: aa8-30, aa884-895, aa1173-1192, aa2654-2677
Concentration 1mg/mL
Formulation 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl.
Molecular Weight (kDa) 303
Notes Stored in 0.1% sodium azide
Positive Control Whole-cell or Chromatin extracts of HeLa or HEK293 cells
Research Area Epigenetics & Nuclear Signalling, Neurobiology

References

There are 2 reference entries for this reagent.

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References: 2 entries

Yüce et al. 2013. Mol Cell Biol. 33(2):406-17. PMID: 23149945.

Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response.

Europe PMC ID: 23149945


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References: 2 entries

Yüce et al. 2013. Mol Cell Biol. 33(2):406-17. PMID: 23149945.

Senataxin, defective in the neurodegenerative disorder ataxia with oculomotor apraxia 2, lies at the interface of transcription and the DNA damage response.


Add a reference