Rad21 Mouse shRNA Plasmid (Locus ID 19357)
CAT#: TL501846
Rad21 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
Need custom shRNA service?
Get a free quote
CNY 5,740.00
货期*
现货
规格
Cited in 1 publication. |
Product images
经常一起买 (3)
Specifications
Product Data | |
Product Name | Rad21 Mouse shRNA Plasmid (Locus ID 19357) |
Locus ID | 19357 |
UniProt ID | Q61550 |
Synonyms | mKIAA0078; SCC1 |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | Rad21 - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 19357). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | BC043032, BC129916, BC129917, NM_009009, NM_009009.1, NM_009009.2, NM_009009.3, NM_009009.4 |
Summary | Double-strand-break repair protein rad21 homolog: As a member of the cohesin complex, involved in sister chromatid cohesion from the time of DNA replication in S phase to their segregation in mitosis, a function that is essential for proper chromosome segregation, post-replicative DNA repair, and the prevention of inappropriate recombination between repetitive regions. The cohesin complex may also play a role in spindle pole assembly during mitosis (By similarity). In interphase, cohesins may function in the control of gene expression by binding to numerous sites within the genome (PubMed:18237772). May control RUNX1 gene expression. Binds to and represses APOB gene promoter (By similarity). May play a role in embryonic gut development, possibly through the regulation of enteric neuron development (By similarity).[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. |
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: |
---|
ASXL1 interacts with the cohesin complex to maintain chromatid separation and gene expression for normal hematopoiesis
,Li, Z;Zhang, P;Yan, A;Guo, Z;Ban, Y;Li, J;Chen, S;Yang, H;He, Y;Li, J;Guo, Y;Zhang, W;Hajiramezanali, E;An, H;Fajardo, D;Harbour, JW;Ruan, Y;Nimer, SD;Yu, P;Chen, X;Xu, M;Yang, FC;,
Sci Adv
,PubMed ID 28116354
[RAD21]
|
Documents
Product Manuals |
FAQs |
SDS |
Customer
Reviews
Loading...