superscript iii reverse transcription kit (Thermo Fisher)
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90
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superscript iii reverse transcription kit
Superscript Iii Reverse Transcription Kit, supplied by Thermo Fisher, 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/superscript%E2%84%A2+iii+reverse+transcript+kit/high+capacity+cdna+reverse+transcription+kit/pm40571871-100-25-33
Average 90 stars, based on 1 article reviews
Superscript Iii Reverse Transcription Kit, supplied by Thermo Fisher, 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/superscript%E2%84%A2+iii+reverse+transcript+kit/high+capacity+cdna+reverse+transcription+kit/pm40571871-100-25-33
Average 90 stars, based on 1 article reviews
superscript iii reverse transcription kit - by Bioz Stars,
2026-09
90/100 stars
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Isolation:Article Title: Role of AP-1 and RE-1 binding sites in matrix metalloproteinase-2 transcriptional regulation in skeletal muscle atrophy. Article Snippet: 0006-291X/$ see front matter Published by Elsevier doi:10.1016/j.bbrc.2010.04.067 * Corresponding author at: San Francisco Veter Department of Veterans Affairs, 4150 Clement Stre 94121, USA.. Fax: +1 415 75 Article Title: Surface display and characterization of recombinant α-l-Rhamnosidase from Emiliania huxleyi on Pichia pastoris. Article Snippet: An α-L-Rhamnosidase gene with an open reading frame of 3192 bp encoding a 1036-amino acid protein (EhRha) was cloned from Emiliania huxleyi for flavonoid hydrolysis on the cell surface of Pichia pastoris (P. pastoris) strain GS115 by fusing with the anchor protein (AGα1) from Saccharomyces cerevisiae.. Fluorescence microscopy and flow cytometry assays revealed that EhRha was successfully displayed on the cell surface of P. pastoris GS115.. The enzyme activity assay and substrate specificity analysis showed that the enzyme activity of displayed EhRha was 78 U/g (cell wet weight). Synthesized:Article Title: Role of AP-1 and RE-1 binding sites in matrix metalloproteinase-2 transcriptional regulation in skeletal muscle atrophy. Article Snippet: 0006-291X/$ see front matter Published by Elsevier doi:10.1016/j.bbrc.2010.04.067 * Corresponding author at: San Francisco Veter Department of Veterans Affairs, 4150 Clement Stre 94121, USA.. Fax: +1 415 75 Article Title: Surface display and characterization of recombinant α-l-Rhamnosidase from Emiliania huxleyi on Pichia pastoris. Article Snippet: An α-L-Rhamnosidase gene with an open reading frame of 3192 bp encoding a 1036-amino acid protein (EhRha) was cloned from Emiliania huxleyi for flavonoid hydrolysis on the cell surface of Pichia pastoris (P. pastoris) strain GS115 by fusing with the anchor protein (AGα1) from Saccharomyces cerevisiae.. Fluorescence microscopy and flow cytometry assays revealed that EhRha was successfully displayed on the cell surface of P. pastoris GS115.. The enzyme activity assay and substrate specificity analysis showed that the enzyme activity of displayed EhRha was 78 U/g (cell wet weight). |