the bluescript sk1 vector (Agilent technologies)
90
Structured Review
Agilent technologies
the bluescript sk1 vector
The Bluescript Sk1 Vector, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bluescript+sk1-vector/pm10828066-57-32-35
Average 90 stars, based on 1 article reviews
The Bluescript Sk1 Vector, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bluescript+sk1-vector/pm10828066-57-32-35
Average 90 stars, based on 1 article reviews
the bluescript sk1 vector - by Bioz Stars,
2026-09
90/100 stars
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Expressing:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the Functional Assay:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the Amplification:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the Polymerase Chain Reaction:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the Sequencing:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the Clone Assay:Article Title: Binding of Ca2+ and Zn2+ to Human Nuclear S100A2 and Mutant Proteins Article Snippet: Construction of Wild Type and Mutated Expression Vectors—To replace one or both of the functional Ca21 N- or C-terminal domain) of wtS100A2 (GenBankTM/EMBL accession number M87068) by a canonical loop (EF-domain) of human a-PV, the human cDNA (GenBankTM/ EMBL accession number X63070) was amplified by PCR on PerkinElmer and Hybaid Omni-Gene thermal cyclers, using specific oligonucleotides spanning the sequence of the EF-site of PV and specific restriction sites for subsequent cloning into the |