NME2 Human shRNA Plasmid Kit (Locus ID 4831)
CAT#: TR311160
NME2 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CNY 4,790.00
货期*
现货
规格
Cited in 1 publication. |
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Specifications
Product Data | |
Product Name | NME2 Human shRNA Plasmid Kit (Locus ID 4831) |
Locus ID | 4831 |
UniProt ID | P22392 |
Synonyms | NDKB; NDPK-B; NDPKB; NM23-H2; NM23B; PUF |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | NME2 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 4831). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001018137, NM_001018138, NM_001018139, NM_001198682, NM_002512, NM_001018139.1, NM_001018139.2, NM_002512.1, NM_002512.2, NM_002512.3, NM_001018137.1, NM_001018137.2, NM_001018138.1, NM_001198682.1, BC002476, BC002476.2, BC095458, BM556410, NM_001198682.2, NM_001018137.3, NM_002512.4 |
Summary | Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by NME1) and 'B' (encoded by this gene) isoforms. Multiple alternatively spliced transcript variants have been found for this gene. Read-through transcription from the neighboring upstream gene (NME1) generates naturally-occurring transcripts (NME1-NME2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Nov 2010] |
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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Promoter-proximal transcription factor binding is transcriptionally active when coupled with nucleosome repositioning in immediate vicinity
,Yadav, VK;Thakur, RK;Eckloff, B;Baral, A;Singh, A;Halder, R;Kumar, A;Alam, MP;Kundu, TK;Pandita, R;Pandita, TK;Wieben, ED;Chowdhury, S;,
Nucleic Acids Res. July 2014
,PubMed ID 25081206
[NME2]
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