Non Neuronal Enolase (ENO1) Human shRNA Plasmid Kit (Locus ID 2023)
CAT#: TL313211
ENO1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
Need custom shRNA service?
Get a free quote
CNY 5740.00
Cited in 1 publication. |
Product images

CNY 4070.00
Specifications
Product Data | |
Product Name | Non Neuronal Enolase (ENO1) Human shRNA Plasmid Kit (Locus ID 2023) |
Locus ID | 2023 |
UniProt ID | P06733 |
Synonyms | ENO1L1; HEL-S-17; MPB1; NNE; PPH |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | ENO1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 2023). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_001201483, NM_001428, NM_001353346, NM_001428.1, NM_001428.2, NM_001428.3, NM_001201483.1, BC022545, BC022545.1, BC001810, BC004325, BC004458, BC009218, BC009912, BC011130, BC015641, BC021166, BC027725, BC050642, BC113034, NM_001428.5, NM_001201483.4 |
Summary | This gene encodes alpha-enolase, one of three enolase isoenzymes found in mammals. Each isoenzyme is a homodimer composed of 2 alpha, 2 gamma, or 2 beta subunits, and functions as a glycolytic enzyme. Alpha-enolase in addition, functions as a structural lens protein (tau-crystallin) in the monomeric form. Alternative splicing of this gene results in a shorter isoform that has been shown to bind to the c-myc promoter and function as a tumor suppressor. Several pseudogenes have been identified, including one on the long arm of chromosome 1. Alpha-enolase has also been identified as an autoantigen in Hashimoto encephalopathy. [provided by RefSeq, Jan 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: |
---|
Dominant role of CDKN2B/p15INK4B of 9p21.3 tumor suppressor hub in inhibition of cell-cycle and glycolysis
,Xia, Y;Liu, Y;Yang, C;Simeone, DM;Sun, TT;DeGraff, DJ;Tang, MS;Zhang, Y;Wu, XR;,
Nature communications
,PubMed ID 33824349
[ENO1]
|
Documents
Product Manuals |
FAQs |
SDS |