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Adprh Mouse shRNA Plasmid (Locus ID 11544)

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SKU
TG512261
Adprh - Mouse, 4 unique 29mer shRNA constructs in retroviral GFP vector, 5µg of each construct provided
  $883.00
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Specifications
Specifications
Product Data
Locus ID 11544
Synonyms Arh1
Vector pGFP-V-RS
E. coli Selection Kanamycin
Mammalian Cell Selection Puromycin
Format Retroviral plasmids
Components Adprh - Mouse, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 11544). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free.
RefSeq BC003437, NM_007414, NM_007414.1, NM_007414.2, NM_007414.3, BC058232
UniProt ID P54923
Summary Specifically acts as a arginine mono-ADP-ribosylhydrolase by mediating the removal of mono-ADP-ribose attached to arginine residues on proteins.UniProtKB/Swiss-Prot Function
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

Role of a TRIM72 ADP-ribosylation cycle in myocardial injury and membrane repair
Ishiwata-Endo, Kato, Tonouchi et al
JCI Insight (2018) 3 (22) DOI: 10.1172/jci.insight.97898
AI Summary: OriGene products contributed to this study by providing shRNA vectors targeting ARH1, ART1, TRIM72, and control sequences, which were used to generate C2C12 cell lines for investigating the role of these genes in membrane repair and wound healing.
Snippet: and used at approximately 80% confluence to avoid effects of cell contact. Scratch wound healing assay. C2C12 cells were prepared that stably expressed ARH1, ART1, TRIM72, and control shRNA vectors (Origene) and transiently overexpressed pEGFP-N1-TRIM72 and pEGFP-N1-TRIM72 (R207K, R260K) vectors. The cells were scratched by needle at confluence, and wound-healing ability was assessed at 0, 8, 16,
Showing 1-1 of 1 papers.
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