Runx2 Mouse shRNA Plasmid (Locus ID 12393)
CAT#: TF510502
Runx2 - Mouse, 4 unique 29mer shRNA constructs in retroviral RFP vector, 5µg of each construct provided
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CNY 4,790.00
货期*
现货
规格
Cited in 4 publications. |
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经常一起买 (1)
Specifications
Product Data | |
Product Name | Runx2 Mouse shRNA Plasmid (Locus ID 12393) |
Locus ID | 12393 |
UniProt ID | Q08775 |
Synonyms | AM; AML3; Cbf; Cbfa; Cbfa-1; Cbfa1; LS3; Os; Osf2; PEB; Pebp2a1; PEBP2aA; Pebpa2a |
Vector | pRFP-C-RS |
Format | Retroviral plasmids |
Kit Components | Runx2 - Mouse, 4 unique 29mer shRNA constructs in retroviral RFP vector(Gene ID = 12393). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRFP-C-RS Vector, TR30015, included for free. |
RefSeq | NM_001145920, NM_001146038, NM_001271627, NM_001271630, NM_001271631, NM_009820, NR_073392, NR_073425, NM_001146038.1, NM_001146038.2, NM_009820.1, NM_009820.2, NM_009820.3, NM_009820.4, NM_009820.5, NM_001145920.1, NM_001145920.2, NM_001271631.1, NM_001271630.1, NM_001271627.1, BC172607, BC172715, NM_001271633 |
Summary | This gene encodes a member of the runt domain-containing family of transcription factors. This protein is essential for osteoblastic differentiation and skeletal morphogenesis and acts as a scaffold for nucleic acids and regulatory factors involved in skeletal gene expression. The protein can bind DNA both as a monomer or, with more affinity, as a subunit of a heterodimeric complex. Transcript variants that encode different protein isoforms result from the use of alternate promoters as well as alternate splicing. [provided by RefSeq, Sep 2015] |
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 (4)
The use of this RNAi has been cited in the following citations: |
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Mapping Distinct Bone Marrow Niche Populations and Their Differentiation Paths
,null,
Cell reports
,PubMed ID 31291568
[Runx2]
|
Neural EGFL-Like 1 Regulates Cartilage Maturation through Runt-Related Transcription Factor 3–Mediated Indian Hedgehog Signaling
,null,
The American Journal of Pathology
,PubMed ID 29137952
[Runx2]
|
Nfatc1 Is a Functional Transcriptional Factor Mediating Nell-1-Induced Runx3 Upregulation in Chondrocytes
,null,
International Journal of Molecular Sciences
,PubMed ID 29316655
[Runx2]
|
Glucocorticoid-mediated BIM induction and apoptosis are regulated by Runx2 and c-Jun in leukemia cells
,null,
Cell Death & Disease
,PubMed ID 22825467
[Runx2]
|
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