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PrimerDesign Inc quickchange primer design tool
Quickchange Primer Design Tool, supplied by PrimerDesign Inc, 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/quickchange+primer+design+program/quickchange+primer+design+program/pmc03585152-94-23-24
Average 90 stars, based on 1 article reviews
quickchange primer design tool - by Bioz Stars, 2026-11
90/100 stars

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Introduce:

Article Title: The NF1 tumor suppressor regulates PD-L1 and immune evasion in melanoma.
Article Snippet: Site-directed mutagenesis of the HA-GRD in pDONR223 was conducted using the QuickChange II XL Site-Directed Mutagenesis Kit (Agilent, 200521) as per the manufacturer’s protocol to generate HA-dGRD pDONR223. .. Primers to introduce the desired mutations were designed using the QuickChange Primer Design Program and purchased from Sigma-Aldrich. .. All HA-tagged NF1 truncations were subcloned into the pHAGE EF1a and pLenti6/V5DEST Gateway Vector (Invitrogen, V49610) destination vectors with Gateway LR Clonase II Enzyme mix (ThermoFisher Scientific, 11791020). eGFP subcloned into pHAGE EF1a vector was employed to ensure even amounts of DNA were transfected in co-IP experiments. eGFP and LacZ subcloned into pHAGE EF1A and pLenti6.3/V5 vectors were used as controls for overexpression experiments.

other:

Article Title: Engineering affinity of humanized ScFv targeting CD147 antibody: A combined approach of mCSM-AB2 and molecular dynamics simulations.
Article Snippet: This study aims to assess the effectiveness of mCSM-AB2, a graph-based signature machine learning method, for affinity engineering of the humanized single-chain Fv anti-CD147 (HuScFvM6-1B9).. In parallel, molecular dynamics (MD) simulations were used to gain valuable insights into the dynamics and affinity of the HuScFvM61B9-CD147 complex.. The result analysis involved integrating free energy changes calculated from the mCSMAB2 with binding free energy predictions from MD simulations.

Mutagenesis:

Article Title: Characterization of pre-mRNA Splicing Defects Caused by CLCN5 and OCRL Mutations and Identification of Novel Variants Associated with Dent Disease.
Article Snippet: .. Primers for mutagenesis were designed using the bioinformatics tool QuickChange® Primer Design Program (available online: https://www. agilent.com/store/primerDesignProgram.jsp, accessed on 20 October 2019) according to the guidelines described in the QuickChange® commercial kit (Table S1). ..

Article Title: Ubiquitination of gasdermin D N-terminal domain directs its membrane translocation and pore formation during pyroptosis.
Article Snippet: pTRIPZshNS (Addgene, 127696) was received as a gift from Sandra Demaria. .. Truncation mutation or point mutation plasmids were generated using the QuickChange Primer Design Program and mutagenesis kit (Agilent Technologies). .. Truncation mutation or point mutation plasmids were generated using the QuickChange Primer Design Program and mutagenesis kit (Agilent Technologies).

Article Title: Identification of the interfacial regions in misfolded transthyretin oligomers.
Article Snippet: Misfolding and aggregation of transthyretin (TTR) is associated with numerous ATTR amyloidosis.. TTR aggregates extracted from ATTR patients consist of not only full-length TTR, but also N-terminally truncated TTR fragments that can be produced by proteolytic cleavage, suggesting the presence of multiple misfolding pathways.. Here, we report mechanistic studies of an early stage of TTR aggregation to probe the oligomerization process for the full-length as well as N-terminally truncated TTR.

Article Title: Molecular mechanism underlying non-discriminatory recognition of relaxin-3 by RXFP3 and RXFP4.
Article Snippet: To conduct functional assays, RXFP4 and RXFP3were cloned into pCMV6 constructs (OriGene Technologies, Maryland, MD, USA). .. Mutant receptors were generated by site-directed mutagenesis using the wild-type (WT) constructs as templates, with primers designed in Communications Biology | (2025) 8:794 9 QuickChange Primer Design [QuickChange Primer Design (http://agilent. com.cn)] and made by Phanta Max Master (Vazyme, Nanjing, China). ..

Article Title: The BRCA2 R2645G variant increases DNA binding and induces hyper-recombination.
Article Snippet: Materials and methods Site-directed mutagenesis Point mutations ( R2520L, R2645G, R2659G ) were introduced in BRCA2 CTD ( aa 2474–3190 ) or EGFP-MBP-BRCA2 vector using QuikChange II and QuikChange XL site-directed mutagenesis kit ( Agilent Technologies ) , respectively, as previously described ( 28 ) . .. Mutagenesis primers were designed using the QuickChange Primer Design program and purchased from MWG Eurofins. ..

Generated:

Article Title: Ubiquitination of gasdermin D N-terminal domain directs its membrane translocation and pore formation during pyroptosis.
Article Snippet: pTRIPZshNS (Addgene, 127696) was received as a gift from Sandra Demaria. .. Truncation mutation or point mutation plasmids were generated using the QuickChange Primer Design Program and mutagenesis kit (Agilent Technologies). .. Truncation mutation or point mutation plasmids were generated using the QuickChange Primer Design Program and mutagenesis kit (Agilent Technologies).

Article Title: Molecular mechanism underlying non-discriminatory recognition of relaxin-3 by RXFP3 and RXFP4.
Article Snippet: To conduct functional assays, RXFP4 and RXFP3were cloned into pCMV6 constructs (OriGene Technologies, Maryland, MD, USA). .. Mutant receptors were generated by site-directed mutagenesis using the wild-type (WT) constructs as templates, with primers designed in Communications Biology | (2025) 8:794 9 QuickChange Primer Design [QuickChange Primer Design (http://agilent. com.cn)] and made by Phanta Max Master (Vazyme, Nanjing, China). ..

Construct:

Article Title: Molecular mechanism underlying non-discriminatory recognition of relaxin-3 by RXFP3 and RXFP4.
Article Snippet: To conduct functional assays, RXFP4 and RXFP3were cloned into pCMV6 constructs (OriGene Technologies, Maryland, MD, USA). .. Mutant receptors were generated by site-directed mutagenesis using the wild-type (WT) constructs as templates, with primers designed in Communications Biology | (2025) 8:794 9 QuickChange Primer Design [QuickChange Primer Design (http://agilent. com.cn)] and made by Phanta Max Master (Vazyme, Nanjing, China). ..

Article Title: Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation.
Article Snippet: Mutagenesis was performed using the Q5 proofreading DNA polymerase (New England Biolabs) and a standard protocol. .. The primers used (Supplemental Table 1) were designed using the QuickChange Primer Design Program and have been described in detail elsewhere.38 Final constructs were sequence-verified. ..

Sequencing:

Article Title: Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation.
Article Snippet: Mutagenesis was performed using the Q5 proofreading DNA polymerase (New England Biolabs) and a standard protocol. .. The primers used (Supplemental Table 1) were designed using the QuickChange Primer Design Program and have been described in detail elsewhere.38 Final constructs were sequence-verified. ..



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