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Pcmv6 xl4 src

Manufactured by OriGene

The PCMV6-XL4-SRC is a plasmid that contains the coding sequence for the Src proto-oncogene. This plasmid can be used for expression of the Src protein in various cell lines.

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2 protocols using pcmv6 xl4 src

1

Constructing ERBB1 Expression Plasmid

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To construct pCMV6-XL5-ERBB1 which expresses human ERBB1, the full length human ERBB1 coding sequence was amplified by PCR from LNCaP cDNA using Kpn1-forward primer (5′-GGTACCCGGCCCCCTGACTCCGTCCAG-3′) and HindIII-reverse primer (5′-AAGCTTTCATGCTCCAATAAATTCACTGCTTTGTGGC-3′). The amplified PCR product was digested by KpnI and HindIII (New England BioLabs), followed by ligation into pCMV6-XL5 (Origene) which was pre-digested with the same restriction enzymes. The construct was sequenced to ensure the integrity of the entire coding sequence and correct orientation of the gene. We obtained human ERBB3-expressing plasmid (pCMV6-XL4-ERBB3) and human SRC-expressing plasmid (pCMV6-XL4-SRC) from Origene. Transient gene transfection was carried out using cells grown in 6-well plates and FuGENE HD (Promega).
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2

Constructing ERBB1 Expression Plasmid

Check if the same lab product or an alternative is used in the 5 most similar protocols
To construct pCMV6-XL5-ERBB1 which expresses human ERBB1, the full length human ERBB1 coding sequence was amplified by PCR from LNCaP cDNA using Kpn1-forward primer (5′-GGTACCCGGCCCCCTGACTCCGTCCAG-3′) and HindIII-reverse primer (5′-AAGCTTTCATGCTCCAATAAATTCACTGCTTTGTGGC-3′). The amplified PCR product was digested by KpnI and HindIII (New England BioLabs), followed by ligation into pCMV6-XL5 (Origene) which was pre-digested with the same restriction enzymes. The construct was sequenced to ensure the integrity of the entire coding sequence and correct orientation of the gene. We obtained human ERBB3-expressing plasmid (pCMV6-XL4-ERBB3) and human SRC-expressing plasmid (pCMV6-XL4-SRC) from Origene. Transient gene transfection was carried out using cells grown in 6-well plates and FuGENE HD (Promega).
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