TDP1 Human shRNA Plasmid Kit (Locus ID 55775)

SKU
TR308891
TDP1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
  $883.00
2 Weeks*
Specifications
Specifications
Product Data
Locus ID 55775
Vector pRS
E. coli Selection Ampicillin
Mammalian Cell Selection Puromycin
Format Retroviral plasmids
Components TDP1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 55775). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free.
RefSeq NM_001008744, NM_001330205, NM_018319, NM_001008744.1, NM_018319.1, NM_018319.2, BC015474, BC015474.1, BC006083, BC107877, BM661793, NM_018319.4, NM_001008744.2
UniProt ID Q9NUW8
Summary The protein encoded by this gene is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. This protein may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains. Mutations in this gene are associated with the disease spinocerebellar ataxia with axonal neuropathy (SCAN1). provided by RefSeq, Aug 2016
shRNA Design These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
Storage Store at -20°C
Shipping Ambient
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Documents
Resources

file-alt Citations

Expression of TDP-43 C-terminal Fragments in Vitro Recapitulates Pathological Features of TDP-43 Proteinopathies
Igaz, Kwong, Chen-Plotkin et al
J Biol Chem (2009) 284 (13), 8516-24 DOI: 10.1074/jbc.M809462200
AI Summary: In this study, OriGene’s TDP-43 expression plasmids (e.g., pCMV6-TDP-43) were used to express TDP-43 C-terminal fragments in cultured cells, enabling the authors to model and analyze pathological features of TDP-43 proteinopathies such as cytoplasmic aggregation, ubiquitination, and abnormal phosphorylation.
Showing 1-1 of 1 papers.
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