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Citations for Takara Bio :
151 - 200 of 629 citations for Forkhead Box N1 FOXN1 Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Cell Biology 2021Quote: Each fluorescent DNM2 construct utilized was cloned into the pEGFP-N1 vector (Clontech) as described in Tassin et al.18 to generate C-terminal EGFP fusion constructs.
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bioRxiv - Cell Biology 2021Quote: ... The human ezrin sequence was cloned into a pEGFP-N1 (Clontech; 6085-1). The human MISP and EGFP-MISP sequences were subcloned into modified pFastBac-6xHis-MBP plasmid LIC expression vector (Addgene ...
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bioRxiv - Cell Biology 2022Quote: Every protein expressed in mouse rods was also cloned into pEGFP-N1 (Clontech) for expression in AD293 cells using the AgeI and NotI cloning sites within the vector to replace EGFP with the tagged proteins ...
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bioRxiv - Cell Biology 2019Quote: ... cDNAs of mCherry and puromycin resistance were amplified from pmCherry-N1 (632523, Clontech) and pICE vector (Addgene #46960)33 ...
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bioRxiv - Developmental Biology 2020Quote: ... digested with EcoRI and BamHI to yield psfGFP-N1-2E12 using InFusion (Takara).
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bioRxiv - Neuroscience 2020Quote: ... the human cytomegalovirus (hCMV) promoter/immediate-early enhancer (IE) of peGFP-N1 (Clontech) and the chimeric intron (chI ...
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bioRxiv - Developmental Biology 2021Quote: Expression vectors for eGFP fusions were generated in eGFP N1 (Clontech, #6085-1) by subcloning of PCR fragments obtained using primers and template vectors shown in Supplemental Table S1 ...
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bioRxiv - Biophysics 2020Quote: ... The mCherry gene (AgeI / NheI) was obtained by PCR on pmCherry-N1 (Clontech). A four-fragment-ligation was then done to obtain the final construct (HindIII-HA-Nlg1-AgeI-mCherry-NheI-Nlg1Cter-NotI) ...
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bioRxiv - Biochemistry 2022Quote: ... The ZIP4 coding sequence was inserted into a modified pEGFP-N1 vector (Clontech) in which the downstream EGFP gene was deleted and an HA tag was added at the C-terminus ...
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bioRxiv - Microbiology 2023Quote: ... HIV-1 NL4-3 Vpu ORF was cloned into pEGFP-N1 (Clontech, France). The ORF of human ATG5 was cloned in frame with HA tag into pAS1B vector (pAS1B-HA-ATG5) ...
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bioRxiv - Cell Biology 2023Quote: ... delCMV- mCherry was generated by ligating the larger fragment from pmCherry-N1 (Clontech) with the smaller fragment from delCMV-mCherry-actin (Schulze et al. ...
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bioRxiv - Neuroscience 2023Quote: ... Cousin lab was dropped into an pEGFP-N1 CMV mammalian expression vector (Clontech) by In-fusion cloning ...
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bioRxiv - Biochemistry 2023Quote: ... The ZIP4 coding sequence was inserted into a modified pEGFP-N1 vector (Clontech) in which the downstream EGFP gene was deleted and an HA tag was added at the C-terminus ...
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bioRxiv - Cell Biology 2023Quote: ... and Biocenter Finland) was cloned into the pEGFP-N1 backbone (Takara Bio Inc.) with XhoI and Kpn1 restriction sites ...
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bioRxiv - Developmental Biology 2024Quote: ... Empty vectors of pEGFP-C1 and pmCherry-N1 were used as controls (Clontech). For overexpression of NDE1 ...
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bioRxiv - Microbiology 2024Quote: ... The coding sequence of YFP was amplified from the plasmid pEYFP-N1 (Clontech) using an upstream primer (YFP_F ...
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bioRxiv - Neuroscience 2021Quote: ... transfected at 5-7 DIV with the plasmid peGFP-N1 (Clontech, Mountain View, CA) using lipofectamine 2000 (ThermoFisher Scientific) ...
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bioRxiv - Cell Biology 2019Quote: ... The following plasmids were used for transfection: pEGFP-N1 (Clontech Cat. No. 6085-1), pCDNA3.1 N-Myc-TNAP and pCDNA3-mCherry TNAP ...
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bioRxiv - Cell Biology 2019Quote: ... β2AR-mCherry was made by transferring β2AR from β2AR-mCFP to pmCherry-N1 (Clontech) using NheI/XhoI ...
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bioRxiv - Cell Biology 2019Quote: ... LAMP1-GFP was made by transferring LAMP1 from LAMP1-mCherry into pEGFP-N1 (Clontech) using EcoRI/BamHI ...
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bioRxiv - Cell Biology 2019Quote: H2B-mCh was made by transferring H2B from H2B-GFP to pmCherry-N1 (Clontech) using KpnI/BamHI ...
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bioRxiv - Immunology 2019Quote: ... Expression vectors are based on pEGFP-n1 or pEGFP-c1 (Clontech, Mountain View, CA). The VSV-G pseudotyping vector pMD2.G and the viral packaging vector psPAX2 were gifts from Didier Trono (Addgene plasmids #12259 and #12260) ...
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bioRxiv - Cell Biology 2019Quote: ... cut with EcoR I and Xho I and then inserted into pEGFP-N1 (Clontech). The construct was verified by DNA sequencing.
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bioRxiv - Cell Biology 2020Quote: ... Universal donor vector (pCassette) was generated by restriction digest of pEGFP-N1 vector (Clontech) to insert a new multiple cloning site as previously described16 ...
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bioRxiv - Microbiology 2019Quote: ... was first produced by modifying a CMV-driven eGFP cassette from pEGFP-N1 (Clontech), such that the CMV immediate early promoter was partially duplicated with an iscei::kan cassette inserted between the duplicated sequences ...
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bioRxiv - Immunology 2021Quote: ... Full length of WT mHVEM and mutants were cloned into pmCherry-N1 vector (Clontech), respectively ...
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bioRxiv - Immunology 2021Quote: ... The cDNA of SHP-1 was subcloned into the expression vector pEYFP-N1(Clontech) to obtain the chimeric protein YFP-SHP-1 ...
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bioRxiv - Biophysics 2022Quote: ... and human CaMKIIK42RD135N with a C-terminal AviTag were cloned into pEGFP-N1 (Clontech) vector ...
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bioRxiv - Molecular Biology 2023Quote: ... were subcloned in frame from their corresponding SMAUG1-HisTEV2xFLAG plasmids into pEGFP-N1 (Clontech) using XhoI and BamHI ...
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bioRxiv - Genomics 2023Quote: ... cells were co-transfected with 1 µg of pEGFP-N1 plasmid (Takara Bio USA). Where indicated ...
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bioRxiv - Developmental Biology 2023Quote: ... The PCR amplified cDNA fragments were cloned into PEGF-N1 vector (Clontech,6085-1,) with XhoI/BamhI enzyme sites ...
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bioRxiv - Cell Biology 2023Quote: ... and CEP44 mutants were amplified via PCR and cloned into pEGFP-N1 (Clontech Laboratories) and p3×FLAG-CMV-14 (Sigma-Aldrich) ...
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bioRxiv - Cell Biology 2023Quote: ... Human CXCR4 was cloned into the pAcGFPm-N1 plasmid (Clontech Laboratories, Palo Alto, CA), as described (20).
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bioRxiv - Cell Biology 2024Quote: ... the annealed LifeAct was fused to N-terminal of mCherry-N1 vectors (Takara, #632523). Generation of pFN21A-HaloTag-actin was described previously21.
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bioRxiv - Cell Biology 2021Quote: ... was constructed similarly by placing the HRAS-CAAX box motif on the C-terminus of EGFP in the pEGP-C1 vector (Clontech). The RFP-Myo10 construct was prepared by cloning mApple (from Addgene No ...
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bioRxiv - Cell Biology 2021Quote: ... The XPack-GFP plasmid was generated by inserting GFP from pEGFP-N1 (BD Biosciences Clontech) into the XPack CMV-XP-MCS-EF1α-Puro Cloning Lentivector (System Biosciences ...
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bioRxiv - Biochemistry 2019Quote: The TPP1 coding sequence was previously cloned into a pmCherry-N1 vector backbone (Clontech, CA) in place of the pmCherry coding sequence 23 ...
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bioRxiv - Developmental Biology 2019Quote: ... and cloned downstream of the EGFP expression cassette on pEGFP-N1 vector (Takara Bio, USA) to generate each pEGFP-Bmp15-shRNA expression vector (Fig ...
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bioRxiv - Molecular Biology 2019Quote: ... The PCR product was cloned into the corresponding restriction sites of pEGFP-N1 vector (Clontech).
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bioRxiv - Synthetic Biology 2019Quote: ... then assembled and inserted into pEGFP-N1 at NheI and NotI using In-Fusion (Clontech). These plasmids have been deposited with Addgene.
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bioRxiv - Biophysics 2021Quote: ... Protein constructs were expressed under control of a CMV promoter using pEGFP-C1/N1 (Clontech) (enhanced GFP ...
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bioRxiv - Neuroscience 2020Quote: ... The sequences were inserted into either the pEGFP-N1 vector (Clontech, Mountain View, CA, USA) or one modified to contain the -HA epitope using primers containing restriction sites.
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bioRxiv - Molecular Biology 2020Quote: ... The tIE2.1 and tIE2.2 promoter fragments were then cloned into pEGFP-N1 vector (Clontech, USA) to produce pCMV/tIE2.1 and pCMV/tIE2.2 vectors ...
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bioRxiv - Biochemistry 2022Quote: ... DNA-lipid complexes were prepared by incubating 100 ng of eGFP-N1 plasmid (Takara Biosciences) with Lipofectamine 2000 for 20 min ...
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bioRxiv - Cancer Biology 2022Quote: ... These clones were further tested for transfectability using pmCherry-N1 control vectors (Takara Bio #632523). 200’000 cells of selected monocolonies of either cell line were seeded in 6-well plates and transfected on next day with CRISPR plasmids using Lipofectamine 2000 (Invitrogen by Life Technologies #11668019 ...
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bioRxiv - Biophysics 2022Quote: HIV-1 Gag (75) was ligated into pEGFP-N1 (Clontech, Takara Bio, Mountain View, CA) to generate the HIV-1 Gag-EGFP vector ...
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bioRxiv - Biophysics 2022Quote: HIV-1 Gag (75) was ligated into pEGFP-N1 (Clontech, Takara Bio, Mountain View, CA) to generate the HIV-1 Gag-EGFP vector ...
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bioRxiv - Cell Biology 2019Quote: ... The LHA was cloned into BglII and AgeI sites of the pEGFP-N1 vector (Clontech). The RHA was subcloned into BsrGI and StuI sites of the pEGFP-N1/LHA construct.
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bioRxiv - Cell Biology 2023Quote: pmCherry-C1 (cat. No. 632524) and pAcGFP-N1 (cat. No. 632469) were purchased from Clontech. dsRed-EEA1-FYVE was a generous gift from Dr ...
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bioRxiv - Neuroscience 2021Quote: ... Neuronal morphology of 14 DIV neurons transfected with the plasmid peGFP-N1 (Clontech, Mountain View, CA) was examined using high-resolution confocal digital images obtained from an Opera-Phenix microscope (Perkin-Elmer) ...