gst/halotag® coding sequence (Promega)
90
Structured Review
Promega
gst/halotag® coding sequence
Gst/Halotag® Coding Sequence, supplied by Promega, 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/gst+coding+sequence/luciferase+coding+sequence/pm36614024-634-8-13
Average 90 stars, based on 1 article reviews
Gst/Halotag® Coding Sequence, supplied by Promega, 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/gst+coding+sequence/luciferase+coding+sequence/pm36614024-634-8-13
Average 90 stars, based on 1 article reviews
gst/halotag® coding sequence - by Bioz Stars,
2026-11
90/100 stars
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Related Articles
Reverse Transcription Polymerase Chain Reaction:Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers. Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag® coding sequence (Flexi® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag ® coding sequence (Flexi ® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Clone Assay:Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers. Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag® coding sequence (Flexi® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag ® coding sequence (Flexi ® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Sequencing:Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers. Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag® coding sequence (Flexi® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag ® coding sequence (Flexi ® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Plasmid Preparation:Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers. Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag® coding sequence (Flexi® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. Article Title: α N -Acetyl β-Endorphin Is an Endogenous Ligand of σ1Rs That Regulates Mu-Opioid Receptor Signaling by Exchanging G Proteins for σ2Rs in σ1R Oligomers Article Snippet: The RT-PCR products were cloned downstream of the GST/HaloTag ® coding sequence (Flexi ® Vector, Promega, Madrid, Spain) and the TEV protease site, and when sequenced, the proteins were identical to the GenBankTM sequences. |