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快速内切酶和修饰酶

快速内切酶和修饰酶

DNA 分子量标准

DNA 分子量标准

蛋白提取、纯化及检测

蛋白提取、纯化及检测

ELISA

ELISA

细胞残留检测

细胞残留检测

pEASY®-Blunt Simple Cloning Kit

目录号: CB111-01

单 价:¥620

规格:
20 rxns
60 rxns
数量:
-
+
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产品详情介绍

pEASY®-Blunt Simple Cloning Vector消除了pEASY®-Blunt Cloning Vector上的多克隆位点,克隆后的PCR产物无法使用pEASY®-Blunt Cloning Vector上多克隆位点的限制性内切酶切下。包含LacZ基因,在含有IPTG和X-gal的平板培养基上,可进行蓝白斑筛选, 适用于平端克隆。

产品组成

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References

1 Wu X, Yu C, Mu W, et al. The structural mechanism for transcription activation by Caulobacter crescentus GcrA[J]. Nucleic Acids Research, 2023.(IF 19.16)

2 Li Y, Du Y, Huai J, et al. The RNA helicase UAP56 and the E3 ubiquitin ligase COP1 coordinately regulate alternative splicing to repress photomorphogenesis in Arabidopsis[J]. The Plant Cell, 2022.(IF 12)

3 Wang X, Liu C, Zhang S, et al. N6-methyladenosine modification of MALAT1 promotes metastasis via reshaping nuclear speckles[J]. Developmental cell, 2021.(IF 10.09)

4 Wang H, Zhang L, Shang Y, et al. Emergence and evolution of highly pathogenic porcine epidemic diarrhea virus by natural recombination of a low pathogenic vaccine isolate and a highly pathogenic strain in the spike gene[J]. Virus evolution, 2020.(IF 5.50)

5 Li L, Fang C, Zhuang N, et al. Structural basis for transcription initiation by bacterial ECF σ factors[J]. Nature communications, 2019.(IF 11.90)

6 Zhang W, Wan H, Feng G, et al. SIRT6 deficiency results in developmental retardation in cynomolgus monkeys[J]. Nature, 2018.(IF 41.57)


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