OGS155
PSF-CMV-UB-FLUC ASCI - FIREFLY LUCIFERASE PLASMID
plasmid vector for molecular cloning
别名:
cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector
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500 ML
¥1,193.48
2.5 L
¥4,463.74
¥1,193.48
预计发货时间2025年4月28日详情
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500 ML
¥1,193.48
2.5 L
¥4,463.74
About This Item
UNSPSC代码:
12352200
NACRES:
NA.85
¥1,193.48
预计发货时间2025年4月28日详情
表单
buffered aqueous solution
分子量
size 7200 bp
菌种筛选
kanamycin
复制起点
pUC (500 copies)
肽切割
no cleavage
启动子
Promoter name: CMV
Promoter activity: constitutive
Promoter type: mammalian
报告基因
firefly luciferase
运输
ambient
储存温度
−20°C
1 of 4
此商品 | 100202 | 110983 | 543897 |
|---|---|---|---|
| technique(s) UV/Vis spectroscopy: suitable | technique(s) GC-HS: suitable | technique(s) gas chromatography (GC): suitable | technique(s) HPLC: suitable |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| form liquid | form liquid | form liquid | form liquid |
| UV absorption λ: 270 nm Amax: ≤0.60, λ: 290 nm Amax: ≤0.10, λ: 330 nm Amax: ≤0.01, λ: 275 nm Amax: ≤0.22, λ: 300 nm Amax: ≤0.05 | UV absorption - | UV absorption - | UV absorption - |
| expl. lim. 15.2 % | expl. lim. 15.2 % | expl. lim. 15.2 % | expl. lim. 15.2 % |
一般描述
This plasmid contains a luciferase cassette under the control of the Ub promoter that is designed as an add-on to any of our other plasmids. The Ub luciferase cassette is flanked by AscI sites but is not designed to be split up. If you would like the luciferase gene alone or the Ub promoter alone please see the reporter gene section or the promoter section on our website. The Ub promoter is a relatively strong promoter. Its strength is approximately 10-fold lower than the CMV promoter but 10-fold stronger than the SV40 promoter. We have a weaker Rous Sarcoma virus promoter driven plasmid in the same format if you require an expression vector with lower levels of reporter gene activity.
Promoter Expression Level: This plasmid contains the mammalian CMV promoter to drive gene expression. We have tested all of our mammalian promoters in a range of cell types and CMV is consistently the strongest in those we have studied. However there are many reports of the CMV promoter demonstrating silencing by methylation in long-term culture.
Promoter Expression Level: This plasmid contains the mammalian CMV promoter to drive gene expression. We have tested all of our mammalian promoters in a range of cell types and CMV is consistently the strongest in those we have studied. However there are many reports of the CMV promoter demonstrating silencing by methylation in long-term culture.
应用
Cloning in a gene: This plasmid has been designed to be compatible with a range of cloning techniques. The multiple cloning site contains a range of standard commonly used restriction sites for cloning. Using these sites genes can be inserted using standard cloning methods with DNA ligase. Other methods such as ligase independent cloning (LIC) Gibson Assembly InFusionHD or Seamless GeneArt can also be used and because all of our plasmids are based on the same backbone the same method can be used for cloning into all of our catalogue vectors.
Multiple cloning site notes: There are a few important sites within the MCS. These include the NcoI site the XbaI site and the BsgI and BseRI sites. The NcoI site contains a start codon that is immediately downstream of both a Kozak and Shine-Dalgarno ribosomal binding site. These allow for optimal positioning of genes when the start codon is placed in this location. If this is not required and you wish to use a downstream site for gene cloning you can remove the NcoI site by cleaving the plasmid with KpnI.
The XbaI site contains a stop codon. This stop codon is positioned in a specific position in relation to the BsgI and BseRI sites that are immediately downstream. When either BseRI or BsgI cleave the plasmid they produce a TA overhang from the stop codon in the XbaI site that is compatible with all of our peptide tag plasmids cut with the same sites. BseRI and BsgI sites are non-palindromic and cleave a defined number of bases away from their binding site.
Whenever we clone a gene into our multiple cloning site we always position the start and stop codon in the same positions in the MCS. If the start and ends of the genes are not compatible with NcoI and XbaI we extend the sequence to the nearest external sites but keep the start and stop codons locations consistent.
Multiple cloning site notes: There are a few important sites within the MCS. These include the NcoI site the XbaI site and the BsgI and BseRI sites. The NcoI site contains a start codon that is immediately downstream of both a Kozak and Shine-Dalgarno ribosomal binding site. These allow for optimal positioning of genes when the start codon is placed in this location. If this is not required and you wish to use a downstream site for gene cloning you can remove the NcoI site by cleaving the plasmid with KpnI.
The XbaI site contains a stop codon. This stop codon is positioned in a specific position in relation to the BsgI and BseRI sites that are immediately downstream. When either BseRI or BsgI cleave the plasmid they produce a TA overhang from the stop codon in the XbaI site that is compatible with all of our peptide tag plasmids cut with the same sites. BseRI and BsgI sites are non-palindromic and cleave a defined number of bases away from their binding site.
Whenever we clone a gene into our multiple cloning site we always position the start and stop codon in the same positions in the MCS. If the start and ends of the genes are not compatible with NcoI and XbaI we extend the sequence to the nearest external sites but keep the start and stop codons locations consistent.
序列
To view sequence information for this product, please visit the product page
分析说明
To view the Certificate of Analysis for this product, please visit www.oxgene.com
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产品编号
说明
价格
储存分类代码
12 - Non Combustible Liquids
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
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