BMX Human shRNA Plasmid Kit (Locus ID 660)
CAT#: TR320275
BMX - 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 2 publications. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | BMX Human shRNA Plasmid Kit (Locus ID 660) |
Locus ID | 660 |
UniProt ID | P51813 |
Synonyms | ETK; PSCTK2; PSCTK3 |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | BMX - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 660). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001320866, NM_001721, NM_203281, NM_203281.1, NM_203281.2, NM_001721.1, NM_001721.2, NM_001721.3, NM_001721.4, NM_001721.6, BC016652, BC016652.2, NM_001721.7, NM_203281.3 |
Summary | This gene encodes a non-receptor tyrosine kinase belonging to the Tec kinase family. The protein contains a PH-like domain, which mediates membrane targeting by binding to phosphatidylinositol 3,4,5-triphosphate (PIP3), and a SH2 domain that binds to tyrosine-phosphorylated proteins and functions in signal transduction. The protein is implicated in several signal transduction pathways including the Stat pathway, and regulates differentiation and tumorigenicity of several types of cancer cells. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016] |
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 (2)
The use of this RNAi has been cited in the following citations: |
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BMX negatively regulates BAK function thereby increasing apoptotic resistance to chemotherapeutic drugs
,Fox, JL;Storey, A;,
Cancer Res.
,PubMed ID 25649765
[BMX]
|
Bone Marrow X Kinase–Mediated Signal Transduction in Irradiated Vascular Endothelium
,Tianxiang Tu, Dinesh Thotala, Ling Geng, Dennis E. Hallahan, and Christopher D. Willey,
Cancer Res., Apr 2008; 68: 2861 - 2869.
[BMX]
|
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