Rad9 (RAD9A) Human shRNA Plasmid Kit (Locus ID 5883)
CAT#: TR309962
RAD9A - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CNY 6,790.00
货期*
2周
规格
Cited in 1 publication. |
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Specifications
Product Data | |
Product Name | Rad9 (RAD9A) Human shRNA Plasmid Kit (Locus ID 5883) |
Locus ID | 5883 |
UniProt ID | Q99638 |
Synonyms | RAD9 |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | RAD9A - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 5883). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001243224, NM_004584, NM_004584.1, NM_004584.2, NM_001243224.1, BC014848, BC014848.1, NM_004584.3 |
Summary | This gene product is highly similar to Schizosaccharomyces pombe rad9, a cell cycle checkpoint protein required for cell cycle arrest and DNA damage repair. This protein possesses 3' to 5' exonuclease activity, which may contribute to its role in sensing and repairing DNA damage. It forms a checkpoint protein complex with RAD1 and HUS1. This complex is recruited by checkpoint protein RAD17 to the sites of DNA damage, which is thought to be important for triggering the checkpoint-signaling cascade. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] |
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. |
Performance Guaranteed | OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred). |
Citations (1)
The use of this RNAi has been cited in the following citations: |
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Rapid and transient recruitment of DNMT1 to DNA double-strand breaks is mediated by its interaction with multiple components of the DNA damage response machinery
,Kyungsoo Ha, Gun Eui Lee, Stela S. Palii, Kevin D. Brown, Yoshihiko Takeda, Kebin Liu, Kapil N. Bhalla, and Keith D. Robertson,
Hum. Mol. Genet., Oct 2010; 10.1093/hmg/ddq451
[RAD9A]
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