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The CAND1 is a laboratory instrument designed for DNA and RNA quantification and analysis. It utilizes fluorescence-based technology to accurately measure the concentration and purity of nucleic acid samples. The CAND1 provides reliable and reproducible results, enabling researchers to make informed decisions about their experimental workflows.

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2 protocols using cand1

1

Knockdown of AKTIP, SGK3 and STAT3

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ON-TARGETplus siRNA targeting human AKTIP, SGK3 and STAT3 as well as SMARTpool ON-TARGETplus siRNA targeting 10 AKTIP-bound proteins were purchased from Dharmacon (Lafayette, CO). ESR1, CAND1, FASN and USP7 siRNA were obtained from Integrated DNA Technologies (Coraville, IA). The siRNA sequences are listed in Table S3. Lipofectamine RNAiMAX (Invitrogen, Carlsbad, CA) was used to transfect siRNA at 10 nM. shRNA against AKTIP in pLKO.1-Puro lentiviral vector was developed by The RNAi Consortium (TRC).87 (link) pcDNA3-myc3-CUL2 and pcDNA3-myc3-NEDD8 were gifts from Yue Xiong (Addgene plasmid # 19892 and # 19943).84 (link),85 (link) Transfection of plasmids was performed using Lipofectamine 3000 (Invitrogen). MCF7 cells stably expressing AKTIP shRNA or vector control were established by lentiviral transduction followed by puromycin selection.
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2

Knockdown of AKTIP, SGK3 and STAT3

Check if the same lab product or an alternative is used in the 5 most similar protocols
ON-TARGETplus siRNA targeting human AKTIP, SGK3 and STAT3 as well as SMARTpool ON-TARGETplus siRNA targeting 10 AKTIP-bound proteins were purchased from Dharmacon (Lafayette, CO). ESR1, CAND1, FASN and USP7 siRNA were obtained from Integrated DNA Technologies (Coraville, IA). The siRNA sequences are listed in Table S3. Lipofectamine RNAiMAX (Invitrogen, Carlsbad, CA) was used to transfect siRNA at 10 nM. shRNA against AKTIP in pLKO.1-Puro lentiviral vector was developed by The RNAi Consortium (TRC).87 (link) pcDNA3-myc3-CUL2 and pcDNA3-myc3-NEDD8 were gifts from Yue Xiong (Addgene plasmid # 19892 and # 19943).84 (link),85 (link) Transfection of plasmids was performed using Lipofectamine 3000 (Invitrogen). MCF7 cells stably expressing AKTIP shRNA or vector control were established by lentiviral transduction followed by puromycin selection.
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