ELAVL1 Human shRNA Plasmid Kit (Locus ID 1994)

SKU
TR313235
ELAVL1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
  $883.00
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Specifications
Specifications
Product Data
Locus ID 1994
Synonyms ELAV1; Hua; HUR; MelG
Vector pRS
E. coli Selection Ampicillin
Mammalian Cell Selection Puromycin
Format Retroviral plasmids
Components ELAVL1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 1994). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free.
RefSeq NM_001419, NM_001419.1, NM_001419.2, BC003376, BC003376.2, BM664469, BM696191, NM_001419.3
UniProt ID Q15717
Summary The protein encoded by this gene is a member of the ELAVL family of RNA-binding proteins that contain several RNA recognition motifs, and selectively bind AU-rich elements (AREs) found in the 3' untranslated regions of mRNAs. AREs signal degradation of mRNAs as a means to regulate gene expression, thus by binding AREs, the ELAVL family of proteins play a role in stabilizing ARE-containing mRNAs. This gene has been implicated in a variety of biological processes and has been linked to a number of diseases, including cancer. It is highly expressed in many cancers, and could be potentially useful in cancer diagnosis, prognosis, and therapy. provided by RefSeq, Sep 2012
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
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file-alt Citations

The alternative spliced 3'-UTR mediated differential secretion of macrophage colony stimulating factor in breast cancer cells
Woo, Chambers
Biochem. Biophys. Res. Commun. (2020) 525 (4), 1004-1010 DOI: 10.1016/j.bbrc.2020.03.007
Cited by 1
AI Summary: OriGene's HuR shRNA (TI352933) was used to silence HuR expression in BT20 breast cancer cells, enabling the study of HuR's role in regulating CSF-1 protein secretion mediated by alternative splicing of CSF-1 mRNA 3'UTRs.
Snippet: was used. 2.5. HuR overexpression and silencing in BT20 cells. HuR-pcDNA3.1 was transfected for overexpression. For silencing, HuR shRNA (Origene, TI352933) was transfected. 2.6. CSF-1 sandwich ELISA. Secreted CSF
HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects
Hubers, Valderrama-Carvajal, Laframboise et al
Hum. Mol. Genet. (2011) 20 (3), 553-79 DOI: 10.1093/hmg/ddq500
Cited by 139
AI Summary: In this study, OriGene’s HuD Myc-DDK-tagged cDNA (Cat# RC208307) and SMN Myc-DDK-tagged cDNA (Cat# RC200236) expression plasmids were used to investigate protein interactions and overexpression effects, enabling the authors to demonstrate the role of HuD in rescuing SMA-like neuronal defects.
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Posttranscriptional suppression of proto-oncogene c-fms expression by vigilin in breast cancer
Woo, Yi, Lamb et al
Mol Cell Biol (2011) 31 (1), 215-25 DOI: 10.1128/MCB.01031-10
AI Summary: OriGene products contributed to this study by providing the c-fms expression plasmid (RC200176) and HuR expression plasmid (RC200446), which were used to investigate the regulatory effects of vigilin and HuR on c-fms mRNA and protein expression in breast cancer cells.
Posttranscriptional suppression of proto-oncogene c-fms expression by vigilin in breast cancer
Woo, Yi, Lamb et al
Mol. Cell. Biol. (2011) 31 (1), 215-25 DOI: 10.1128/MCB.01031-10
Cited by 11
AI Summary: In this study, the OriGene shRNA negative control (TR30003) targeting a non-effective 29-nt GFP sequence was used as a control to validate the specificity of vigilin and HuR knockdown experiments investigating their roles in regulating c-fms expression in breast cancer.
Snippet: An shRNA containing a noneffective 29-nt GFP sequence (TR30003, Origene) was used as a negative control [(−) CTRL]. ... We knocked down vigilin or HuR and used immunoprecipitation followed by qRT-PCR to determine the level of endogenous c-fms or luciferase mRNA (in
Regulation of non-AU-rich element containing c-fms proto-oncogene expression by HuR in breast cancer
Woo, Zhou, Yi et al
Oncogene (2009) 28 (9), 1176-86 DOI: 10.1038/onc.2008.469
Cited by 35
AI Summary: OriGene products contributed to this study by providing the c-fms (CSF1R) cDNA clone (OriGene, SC119706), which was used for gene expression and functional analyses to investigate the regulation of c-fms by HuR in breast cancer.
Showing 1-5 of 5 papers.
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