Smc1a Mouse shRNA Plasmid (Locus ID 24061)
CAT#: TL513033
Smc1a - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
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CNY 5,740.00
货期*
现货
规格
Cited in 1 publication. |
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经常一起买 (3)
Specifications
Product Data | |
Product Name | Smc1a Mouse shRNA Plasmid (Locus ID 24061) |
Locus ID | 24061 |
UniProt ID | Q9CU62 |
Synonyms | 5830426I24Rik; mKIAA0178; Sb1.8; SMC-1A; Smc1; Smc1alpha; Smc1l1; Smcb |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | Smc1a - Mouse, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 24061). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | BC131667, NM_019710, NM_019710.1, NM_019710.2, BC003279, BC025590, BC036973, BC055477 |
Summary | Involved in chromosome cohesion during cell cycle and in DNA repair. Involved in DNA repair via its interaction with BRCA1 and its related phosphorylation by ATM, and works as a downstream effector in the ATM/NBS1 branch of S-phase checkpoint (By similarity). Central component of cohesin complex. The cohesin complex is required for the cohesion of sister chromatids after DNA replication. The cohesin complex apparently forms a large proteinaceous ring within which sister chromatids can be trapped. At anaphase, the complex is cleaved and dissociates from chromatin, allowing sister chromatids to segregate. The cohesin complex may also play a role in spindle pole assembly during mitosis. Involved in DNA repair via its interaction with BRCA1 and its related phosphorylation by ATM, or via its phosphorylation by ATR. Works as a downstream effector both in the ATM/NBS1 branch and in the ATR/MSH2 branch of S-phase checkpoint.[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: |
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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
[SMC1A]
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