Parp1 Mouse shRNA Plasmid (Locus ID 11545)

SKU
TL509117
Parp1 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
In Stock*
Specifications
Specifications
Product Data
Locus ID 11545
Synonyms 5830444G22Rik; Adprp; Adprt1; AI893648; ARTD1; C80510; PARP; parp-1; PPOL; sPARP-1
Vector pGFP-C-shLenti
E. coli Selection Chloramphenicol (34 ug/ml)
Mammalian Cell Selection Puromycin
Format Lentiviral plasmids
Components Parp1 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 11545). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq BC012041, NM_007415, NM_007415.1, NM_007415.2, NM_007415.3
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

DNA polymerase theta-mediated DNA repair is a functional dependency and therapeutic vulnerability in DNMT3A deficient leukemia cells
Le, Vekariya, Toma et al
bioRxiv (2024)
Snippet: DY2230AA Addgene Cat#64878 PARP1 mouse shRNA Origene Cat#TL509117 Not available PARP1 mouse ORF Origene Cat# MR211449L4 Not available HUWE1 mouse shRNA Origene Cat#TL503398 Not available MSH2 mouse shRNA Dharmacon Cat# V3SM11241- 234501644 Not available UBE2O mouse siRNA Dharmacon Cat#L-064151-01-0020, (J-064151-09, J0654151-10,J-065
Poly(ADP-ribose) Polymerase 1 Mediates Rab5 Inactivation after DNA Damage
Mashimo, Morozumi, Nobeyama et al
Int J Mol Sci (2022) 23 (14) DOI: 10.3390/ijms23147827
Cited by 5
AI Summary: OriGene's shRNA plasmids targeting human or mouse PARP1, as well as scrambled shRNA controls, were used to manipulate PARP1 expression in NIH3T3 and HeLa cells, enabling the study of PARP1's role in Rab5 inactivation after DNA damage.
Snippet: … Following uptake, some endosomal vesicles are transported to lysosomes for degradation, while the others are returned to the plasma membrane. The destination of these vesicles is d;- shRNA plasmids targeting human or mouse PARP1 or scrambled shRNA (Origene) were introduced into NIH3T3 and HeLa cells using Lipofectamine 3000 transfection Save Cached
FigureFigureFigure
The 89-kDa PARP1 cleavage fragment serves as a cytoplasmic PAR carrier to induce AIF-mediated apoptosis
Mashimo, Onishi, Uno et al
J Biol Chem (2020) 296, 100046 DOI: 10.1074/jbc.RA120.014479
AI Summary: OriGene products contributed to this study by providing shRNA targeting PARP1 and GFP-PARP1 plasmids, which were used to manipulate PARP1 expression and track PARP1 localization in the investigation of apoptosis mechanisms.
Snippet: … Plasmids shRNA targeting PARP1 and GFP-PARP1 were purchased from Origene. PARP1 D214-GFP and PARP1 E988K-GFP were generated with primers (5′-TGGGAGGAGTGGATGAAGTGG-3′ and 5′-CCTCATCGCCTTTTCTCTTTCCTTC-3′) and (5′-AAGTACATTGTCTATGATATTGC-3′ and 5′-GTTATA;- goat anti-mouse and rabbit immunoglobulin from Thermo Fisher Scientific. Plasmids shRNA targeting PARP1 and GFP-PARP1 were purchased from Origene. PARP1 D214-GFP, PARP1 E988K-GFP were generated with primers
Poly(ADP-ribose) contributes to an association between poly(ADP-ribose) polymerase-1 and xeroderma pigmentosum complementation group A in nucleotide excision repair
King, Cooper, Liu et al
J. Biol. Chem. (2012) 287 (47), 39824-33 DOI: 10.1074/jbc.M112.393504
Cited by 5
AI Summary: OriGene’s PARP-1 shRNA (HuSH 29-mer) was used to create PARP-1-silenced cells, enabling the study of PARP-1’s role in nucleotide excision repair in response to UV-induced DNA damage.
Snippet: PARP-1 HuSH cells were created by transfecting HaCaT cells with PARP-1 shRNA (Origene;HuSH 29-mer). ... on retention of UVR-induced photoproducts in cancer-relevant target cells, immortalized human keratinocytes (HaCaT) were transfected with a short hairpin RNA
Arsenite interacts selectively with zinc finger proteins containing C3H1 or C4 motifs
Zhou, Sun, Cooper et al
J. Biol. Chem. (2011) 286 (26), 22855-63 DOI: 10.1074/jbc.M111.232926
Cited by 24
AI Summary: OriGene contributed to this study by providing the PARP-1 expression plasmid, which was used to investigate arsenite's selective binding to zinc finger motifs.
Snippet: Site-directed Mutagenesis and Transfections. A PARP-1 expression plasmid was purchased from OriGene Technologies, Inc. (Rockville, MD), and site-directed mutagenesis of the first and second zinc fingers of PARP-1 was performed by Retrogen, Inc. (San Diego, CA).
Showing 1-5 of 5 papers.
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