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paper n a pcmv6 ac rfp origene ps100034 software  (OriGene)


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    OriGene paper n a pcmv6 ac rfp origene ps100034 software
    Paper N A Pcmv6 Ac Rfp Origene Ps100034 Software, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/Vector+Software/pCMV6-AC-RFP+Mammalian+Expression+Vector/pm42228570-355-74-77
    Average 94 stars, based on 17 article reviews
    paper n a pcmv6 ac rfp origene ps100034 software - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Control:

    Article Title: GPNMB overexpression- a marker of resistance to CDK4/6 inhibitors
    Article Snippet: Lentiviral particles encoding the human GPNMB ORF (NM_001005340, GPNMB Human Tagged Lenti ORF clone, (OriGene cat# RC207615L4V, pLenti-C-mGFP-P2A-Puro) were obtained from OriGEne Technologies (Rockville, MD, USA). .. The pLenti-C-mGFP-P2A-Puro vector (OriGene cat# PS100093V) served as the lentiviral control for all experiments and labeled as empty vector (EV). .. LCC2, MCF7 and T47D cells were transduced with either GPNMB ORF (GPNMB Overexpression, GPNMB-OE) or control lentivirus (Empty Vector-EV) according to the manufacturer’s instructions.

    Labeling:

    Article Title: GPNMB overexpression- a marker of resistance to CDK4/6 inhibitors
    Article Snippet: Lentiviral particles encoding the human GPNMB ORF (NM_001005340, GPNMB Human Tagged Lenti ORF clone, (OriGene cat# RC207615L4V, pLenti-C-mGFP-P2A-Puro) were obtained from OriGEne Technologies (Rockville, MD, USA). .. The pLenti-C-mGFP-P2A-Puro vector (OriGene cat# PS100093V) served as the lentiviral control for all experiments and labeled as empty vector (EV). .. LCC2, MCF7 and T47D cells were transduced with either GPNMB ORF (GPNMB Overexpression, GPNMB-OE) or control lentivirus (Empty Vector-EV) according to the manufacturer’s instructions.

    Immunohistochemical staining:

    Article Title: Immunohistochemical analysis to detect a molecular signature in intervertebral disc degeneration
    Article Snippet: .. For immunohistochemical evaluation, sections were incubated overnight (4 °C) with a primary antibody against FOXO3a (#ab70315, rabbit anti-human, 1:100 dilution; Abcam, Cambridge, UK), SOD2 (#sc-133134, mouse anti-human, 1:100 dilution; Santa Cruz biotech., Dallas, USA), HIF1α (clone H1alpha67, mouse anti-human, 1:200 dilution; Novusbio, Centennial, USA), GLUT1 (#TA301678, mouse anti-human, 1:200 dilution; Origene, Rockville, USA), and BRY (#ab209665, rabbit anti-human, 1:500 dilution; Abcam), followed by treatment with Vectastain ABC solution (#MP-7500; Vectorlabs, Burlingame, USA) for 30 min. To achieve specificity, the working concentrations of primary antibodies were selected by following the dilution guidelines and technical specifications provided by the antibody’s manufacturer. .. Reactions were developed using 3,3′-diaminobenzidine (DAB) solution (Vectorlabs), sections were counterstained with hematoxylin, mounted in glycerol and observed under a bright-field microscope (Nikon Eclipse 50i; objectives: Nikon CFI Achr Adl 10× Ph1 Na 0.25 #MRP40102, Nikon CFI Achr Adl 40× Ph1 Na 0.55 #MRP46402; Nikon Corporation, Tokyo, Japan).

    Incubation:

    Article Title: Immunohistochemical analysis to detect a molecular signature in intervertebral disc degeneration
    Article Snippet: .. For immunohistochemical evaluation, sections were incubated overnight (4 °C) with a primary antibody against FOXO3a (#ab70315, rabbit anti-human, 1:100 dilution; Abcam, Cambridge, UK), SOD2 (#sc-133134, mouse anti-human, 1:100 dilution; Santa Cruz biotech., Dallas, USA), HIF1α (clone H1alpha67, mouse anti-human, 1:200 dilution; Novusbio, Centennial, USA), GLUT1 (#TA301678, mouse anti-human, 1:200 dilution; Origene, Rockville, USA), and BRY (#ab209665, rabbit anti-human, 1:500 dilution; Abcam), followed by treatment with Vectastain ABC solution (#MP-7500; Vectorlabs, Burlingame, USA) for 30 min. To achieve specificity, the working concentrations of primary antibodies were selected by following the dilution guidelines and technical specifications provided by the antibody’s manufacturer. .. Reactions were developed using 3,3′-diaminobenzidine (DAB) solution (Vectorlabs), sections were counterstained with hematoxylin, mounted in glycerol and observed under a bright-field microscope (Nikon Eclipse 50i; objectives: Nikon CFI Achr Adl 10× Ph1 Na 0.25 #MRP40102, Nikon CFI Achr Adl 40× Ph1 Na 0.55 #MRP46402; Nikon Corporation, Tokyo, Japan).

    other:

    Article Title: Identification of cycling regulatory T cell precursors as conductors of immune escape during breast carcinoma progression.
    Article Snippet: Article Identification of cycling regulatory T cell precursors as conductors of immune escape during breast carcinoma progression

    Article Title: Intratumoral microbiota and host genotype cooperatively shape neutrophil cytotoxic functions in colorectal cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Mice strain: NOD-rag-gamma-deficient (NRG) mice NOD.Cg-Rag1tm1Mom Il2rgtm1Wjl/ SzJ, Charles River, Italy) N/A Oligonucleotides Universal bacterial 16S rRNA gene primers; FW- TCCTACGGGAGGCAGCAGT; RWGGACTACCAGGGTATCTAATCCTGTT Microsynth N/A Fusobacterium nucleatum 16s rRNA gene primers; FW- GCCTCACAGCTAGGGACAAC; RWGAGTAAGGGCCGTGTCTCAG Microsynth N/A CXCL1 (human primers): Hs00236937_m1 Applied Biosystems Cat#4331182 CXCL2 (human primers): Hs00236966_m1 Applied Biosystems Cat# 4331182 CXCL5 (human primers): Hs00171085_m1 Applied Biosystems Cat# 4331182 CXL8 (human primers): Hs00174103_m1 Applied Biosystems Cat# 4331182 CD66b (human primers); FW- 5 ′ -TCAAAGCATTTGCAATCAGC-3 ′ ; RW- 5 ′ -GTGGGCAACTTCACAAAGGT-3 ′ Microsynth N/A GAPDH (human primers): Hs02786624_g1 Applied Biosystems Cat#4331182 SIGLEC-14 (human primers); FW: 5 ′ -AGGATTTATTCTCCCATCTCGCT-3 ′ ; RW: 5 ′ -GATGCTGATGGCGAGGTTCTG-3 ′ Sigma-Aldrich N/A SIGLEC-5 (human primers); FW: 5 ′ -GTGGTTCTGACATCTCACCTCATC-3 ′ ; RW: 5 ′ -CCTGAAGATGGTGATGGTCTG-3 ′ Sigma-Aldrich N/A Recombinant DNA pLenti-C-mGFP-P2A-Puro Origene Cat#PS100093 Human SIGLEC5 ORF clone (mGFP-tagged) Origene Cat#RC206610L4 Human SIGLEC14 ORF clone (mGFP-tagged) Origene Cat#RC224202L4 pCMV-dR8.2 Addgene Cat #8455 pVSV-G Addgene Cat#138479 Software and algorithms Adobe Illustrator 27.4 Adobe RRID: SCR_010279 cBioPortal https://www.cbioportal.org N/A CellSense Microscope Imaging Software Olympus N/A clusterProfiler (v4.6.2) Bioconductor RRID:SCR_016884 DoubletFinder (v2.0.6) GitHub RRID:SCR_018301 FACS Diva Software BD Biosciences RRID: SCR_001456 FACS Symphony A5 Cell Analyzer BD Biosciences RRID: SCR_022674 FlowJo v10 + Downsample v3.0.0 + UMAP v2.2 + XShift/Cluster Explorer FlowJo LLC RRID: SCR_008520 GraphPad Prism v8.3.1 GraphPad RRID:SCR_002798 Human Protein Atlas (v23) https://www.proteinatlas.org N/A ImageJ NIH RRID:SCR_003070 ImageJ (FiJi) https://imagej.net/Fiji RRID:SCR_002285 Leiden algorithm Seurat / R N/A MAPS software FEI / Thermo Fisher Scientific N/A PCA Seurat / R RRID:SCR_016341; https://satijalab.org/seurat R (v4.4.3) The R Project RRID:SCR_001905 Seurat (v5.3) Satija Lab / CRAN RRID:SCR_016341 Seurat R package v5.1.0 CRAN/Bioconductor RRID:SCR_016341; https://satijalab.org/seurat (Continued on next page) Cell Host & Microbe 34, 425–443.e1–e11, March 11, 2026 e4

    Over Expression:

    Article Title: Impaired SOX17 Expression Causes Endothelial Dysfunction and Pulmonary Arterial Hypertension by Insufficient Suppression of RUNX1
    Article Snippet: To generate stable SOX17 CRISPR/Cas9 knockout (KO) HPAECs, a single-guide RNA targeting the human SOX17 gene (5′-GTAGTACACGTGAAGGGCGC-3′) was cloned into the lentiCRISPRv2 vector (Addgene plasmid #52961). .. To generate stable RUNX1 overexpression HPAECs, full-length human RUNX1 cDNA (OriGene, Cat# SC123977) was cloned into the pHAGE-EF1α-IRES-blast vector from our lab. High titer lentiviruses were produced at Brown University Legorreta Cancer Center Cell & Genome Engineering Shared Resource. .. HPAECs were transduced at a multiplicity of infection (MOI) of 10 through spinfection, which was performed in the presence of 8 μg/ml polybrene (Sigma-Aldrich, Cat# TR-10003) at 900 g and 32°C for 2 h. The culture medium was replaced 24 h post-transduction, and puromycin antibiotic selection was initiated 5 days post-transduction with a concentration of 0.7 μg/ml.

    Clone Assay:

    Article Title: Impaired SOX17 Expression Causes Endothelial Dysfunction and Pulmonary Arterial Hypertension by Insufficient Suppression of RUNX1
    Article Snippet: To generate stable SOX17 CRISPR/Cas9 knockout (KO) HPAECs, a single-guide RNA targeting the human SOX17 gene (5′-GTAGTACACGTGAAGGGCGC-3′) was cloned into the lentiCRISPRv2 vector (Addgene plasmid #52961). .. To generate stable RUNX1 overexpression HPAECs, full-length human RUNX1 cDNA (OriGene, Cat# SC123977) was cloned into the pHAGE-EF1α-IRES-blast vector from our lab. High titer lentiviruses were produced at Brown University Legorreta Cancer Center Cell & Genome Engineering Shared Resource. .. HPAECs were transduced at a multiplicity of infection (MOI) of 10 through spinfection, which was performed in the presence of 8 μg/ml polybrene (Sigma-Aldrich, Cat# TR-10003) at 900 g and 32°C for 2 h. The culture medium was replaced 24 h post-transduction, and puromycin antibiotic selection was initiated 5 days post-transduction with a concentration of 0.7 μg/ml.

    Produced:

    Article Title: Impaired SOX17 Expression Causes Endothelial Dysfunction and Pulmonary Arterial Hypertension by Insufficient Suppression of RUNX1
    Article Snippet: To generate stable SOX17 CRISPR/Cas9 knockout (KO) HPAECs, a single-guide RNA targeting the human SOX17 gene (5′-GTAGTACACGTGAAGGGCGC-3′) was cloned into the lentiCRISPRv2 vector (Addgene plasmid #52961). .. To generate stable RUNX1 overexpression HPAECs, full-length human RUNX1 cDNA (OriGene, Cat# SC123977) was cloned into the pHAGE-EF1α-IRES-blast vector from our lab. High titer lentiviruses were produced at Brown University Legorreta Cancer Center Cell & Genome Engineering Shared Resource. .. HPAECs were transduced at a multiplicity of infection (MOI) of 10 through spinfection, which was performed in the presence of 8 μg/ml polybrene (Sigma-Aldrich, Cat# TR-10003) at 900 g and 32°C for 2 h. The culture medium was replaced 24 h post-transduction, and puromycin antibiotic selection was initiated 5 days post-transduction with a concentration of 0.7 μg/ml.

    CRISPR:

    Article Title: Activity-regulated circSamm50 modulates mitochondrial dynamics and spine structural plasticity.
    Article Snippet: Four hours after plating, media was replaced with feeding media consisting of Neurobasal media supplemented with Glutamax, Penstrep, and 2% B27 (Invitrogen), and half of the media was replaced every 4 days until the time of experiments at 37◦C with 5% CO2. .. REAGENT or RESOURCE SOURCE IDENTIFIER Samm50 circ_F IDT TCATGAAGCCCGGGAAAAAC Samm50 circ_R IDT CAACTTCCACAAACTCGGCT Foxk2-1157_F IDT CTCCTCCTAACCCTGAACCACA Foxk2-1157_R IDT TCTCTCTTCTCGCTGGATAGGG Foxk2-1357_F IDT ATGTGGTACCCATGCCTACAG Foxk2-1357_R IDT TGCTTCTCTCTCTTCTCGCTG See Table S1-Primers for miRNA primers, CRISPR gRNA, linear RNA primers and insert sequences N/A Recombinant DNA pCMV6-AC-GFP Origene PS100010 pGL3 Basic Luciferase vector Promega E1751 pXR001-mCD4: EF1a-RfxCas13d-P2A-mCD4T2A-EGFP Addgene 228359 Samm50-WT-pGL3 This paper N/A Samm50-MUT-pGL3 This paper N/A circSamm50-WT- pGL3 This paper N/A circSamm50-MUT-pGL3 This paper N/A RCaMP1.07 This paper N/A pCMV6-AC-RFP Origene PS100034 Software and algorithms Graphpad Prism 10 GraphPad Software https://www.graphpad.com/scientific- software/prism/ ImageJ NIH https://imagej.nih.gov/ij/ MATLAB Max Planck, Fl GitHub - ryoheiyasuda/countSpines Fluoview Olympus http://www.olympusconfocal.com/products/ fv1000/fv1000software.html Mitochondria Analyzer NIH https://github.com/AhsenChaudhry/ Mitochondria-Analyzer Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Other CellVis glass-bottom 24-well plate CellVis P24-1.5H-N MatTek No.1 glass coverslip dishes Mattek P35G-1.0-14-C Cell Reports 45, 117378, June 23, 2026 25 ..

    Recombinant:

    Article Title: Activity-regulated circSamm50 modulates mitochondrial dynamics and spine structural plasticity.
    Article Snippet: Four hours after plating, media was replaced with feeding media consisting of Neurobasal media supplemented with Glutamax, Penstrep, and 2% B27 (Invitrogen), and half of the media was replaced every 4 days until the time of experiments at 37◦C with 5% CO2. .. REAGENT or RESOURCE SOURCE IDENTIFIER Samm50 circ_F IDT TCATGAAGCCCGGGAAAAAC Samm50 circ_R IDT CAACTTCCACAAACTCGGCT Foxk2-1157_F IDT CTCCTCCTAACCCTGAACCACA Foxk2-1157_R IDT TCTCTCTTCTCGCTGGATAGGG Foxk2-1357_F IDT ATGTGGTACCCATGCCTACAG Foxk2-1357_R IDT TGCTTCTCTCTCTTCTCGCTG See Table S1-Primers for miRNA primers, CRISPR gRNA, linear RNA primers and insert sequences N/A Recombinant DNA pCMV6-AC-GFP Origene PS100010 pGL3 Basic Luciferase vector Promega E1751 pXR001-mCD4: EF1a-RfxCas13d-P2A-mCD4T2A-EGFP Addgene 228359 Samm50-WT-pGL3 This paper N/A Samm50-MUT-pGL3 This paper N/A circSamm50-WT- pGL3 This paper N/A circSamm50-MUT-pGL3 This paper N/A RCaMP1.07 This paper N/A pCMV6-AC-RFP Origene PS100034 Software and algorithms Graphpad Prism 10 GraphPad Software https://www.graphpad.com/scientific- software/prism/ ImageJ NIH https://imagej.nih.gov/ij/ MATLAB Max Planck, Fl GitHub - ryoheiyasuda/countSpines Fluoview Olympus http://www.olympusconfocal.com/products/ fv1000/fv1000software.html Mitochondria Analyzer NIH https://github.com/AhsenChaudhry/ Mitochondria-Analyzer Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Other CellVis glass-bottom 24-well plate CellVis P24-1.5H-N MatTek No.1 glass coverslip dishes Mattek P35G-1.0-14-C Cell Reports 45, 117378, June 23, 2026 25 ..

    Luciferase:

    Article Title: Activity-regulated circSamm50 modulates mitochondrial dynamics and spine structural plasticity.
    Article Snippet: Four hours after plating, media was replaced with feeding media consisting of Neurobasal media supplemented with Glutamax, Penstrep, and 2% B27 (Invitrogen), and half of the media was replaced every 4 days until the time of experiments at 37◦C with 5% CO2. .. REAGENT or RESOURCE SOURCE IDENTIFIER Samm50 circ_F IDT TCATGAAGCCCGGGAAAAAC Samm50 circ_R IDT CAACTTCCACAAACTCGGCT Foxk2-1157_F IDT CTCCTCCTAACCCTGAACCACA Foxk2-1157_R IDT TCTCTCTTCTCGCTGGATAGGG Foxk2-1357_F IDT ATGTGGTACCCATGCCTACAG Foxk2-1357_R IDT TGCTTCTCTCTCTTCTCGCTG See Table S1-Primers for miRNA primers, CRISPR gRNA, linear RNA primers and insert sequences N/A Recombinant DNA pCMV6-AC-GFP Origene PS100010 pGL3 Basic Luciferase vector Promega E1751 pXR001-mCD4: EF1a-RfxCas13d-P2A-mCD4T2A-EGFP Addgene 228359 Samm50-WT-pGL3 This paper N/A Samm50-MUT-pGL3 This paper N/A circSamm50-WT- pGL3 This paper N/A circSamm50-MUT-pGL3 This paper N/A RCaMP1.07 This paper N/A pCMV6-AC-RFP Origene PS100034 Software and algorithms Graphpad Prism 10 GraphPad Software https://www.graphpad.com/scientific- software/prism/ ImageJ NIH https://imagej.nih.gov/ij/ MATLAB Max Planck, Fl GitHub - ryoheiyasuda/countSpines Fluoview Olympus http://www.olympusconfocal.com/products/ fv1000/fv1000software.html Mitochondria Analyzer NIH https://github.com/AhsenChaudhry/ Mitochondria-Analyzer Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Other CellVis glass-bottom 24-well plate CellVis P24-1.5H-N MatTek No.1 glass coverslip dishes Mattek P35G-1.0-14-C Cell Reports 45, 117378, June 23, 2026 25 ..

    Plasmid Preparation:

    Article Title: Activity-regulated circSamm50 modulates mitochondrial dynamics and spine structural plasticity.
    Article Snippet: Four hours after plating, media was replaced with feeding media consisting of Neurobasal media supplemented with Glutamax, Penstrep, and 2% B27 (Invitrogen), and half of the media was replaced every 4 days until the time of experiments at 37◦C with 5% CO2. .. REAGENT or RESOURCE SOURCE IDENTIFIER Samm50 circ_F IDT TCATGAAGCCCGGGAAAAAC Samm50 circ_R IDT CAACTTCCACAAACTCGGCT Foxk2-1157_F IDT CTCCTCCTAACCCTGAACCACA Foxk2-1157_R IDT TCTCTCTTCTCGCTGGATAGGG Foxk2-1357_F IDT ATGTGGTACCCATGCCTACAG Foxk2-1357_R IDT TGCTTCTCTCTCTTCTCGCTG See Table S1-Primers for miRNA primers, CRISPR gRNA, linear RNA primers and insert sequences N/A Recombinant DNA pCMV6-AC-GFP Origene PS100010 pGL3 Basic Luciferase vector Promega E1751 pXR001-mCD4: EF1a-RfxCas13d-P2A-mCD4T2A-EGFP Addgene 228359 Samm50-WT-pGL3 This paper N/A Samm50-MUT-pGL3 This paper N/A circSamm50-WT- pGL3 This paper N/A circSamm50-MUT-pGL3 This paper N/A RCaMP1.07 This paper N/A pCMV6-AC-RFP Origene PS100034 Software and algorithms Graphpad Prism 10 GraphPad Software https://www.graphpad.com/scientific- software/prism/ ImageJ NIH https://imagej.nih.gov/ij/ MATLAB Max Planck, Fl GitHub - ryoheiyasuda/countSpines Fluoview Olympus http://www.olympusconfocal.com/products/ fv1000/fv1000software.html Mitochondria Analyzer NIH https://github.com/AhsenChaudhry/ Mitochondria-Analyzer Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Other CellVis glass-bottom 24-well plate CellVis P24-1.5H-N MatTek No.1 glass coverslip dishes Mattek P35G-1.0-14-C Cell Reports 45, 117378, June 23, 2026 25 ..

    Software:

    Article Title: Activity-regulated circSamm50 modulates mitochondrial dynamics and spine structural plasticity.
    Article Snippet: Four hours after plating, media was replaced with feeding media consisting of Neurobasal media supplemented with Glutamax, Penstrep, and 2% B27 (Invitrogen), and half of the media was replaced every 4 days until the time of experiments at 37◦C with 5% CO2. .. REAGENT or RESOURCE SOURCE IDENTIFIER Samm50 circ_F IDT TCATGAAGCCCGGGAAAAAC Samm50 circ_R IDT CAACTTCCACAAACTCGGCT Foxk2-1157_F IDT CTCCTCCTAACCCTGAACCACA Foxk2-1157_R IDT TCTCTCTTCTCGCTGGATAGGG Foxk2-1357_F IDT ATGTGGTACCCATGCCTACAG Foxk2-1357_R IDT TGCTTCTCTCTCTTCTCGCTG See Table S1-Primers for miRNA primers, CRISPR gRNA, linear RNA primers and insert sequences N/A Recombinant DNA pCMV6-AC-GFP Origene PS100010 pGL3 Basic Luciferase vector Promega E1751 pXR001-mCD4: EF1a-RfxCas13d-P2A-mCD4T2A-EGFP Addgene 228359 Samm50-WT-pGL3 This paper N/A Samm50-MUT-pGL3 This paper N/A circSamm50-WT- pGL3 This paper N/A circSamm50-MUT-pGL3 This paper N/A RCaMP1.07 This paper N/A pCMV6-AC-RFP Origene PS100034 Software and algorithms Graphpad Prism 10 GraphPad Software https://www.graphpad.com/scientific- software/prism/ ImageJ NIH https://imagej.nih.gov/ij/ MATLAB Max Planck, Fl GitHub - ryoheiyasuda/countSpines Fluoview Olympus http://www.olympusconfocal.com/products/ fv1000/fv1000software.html Mitochondria Analyzer NIH https://github.com/AhsenChaudhry/ Mitochondria-Analyzer Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Zen2.1 SP1 (Black) Carl Zeiss SCR_013672 Other CellVis glass-bottom 24-well plate CellVis P24-1.5H-N MatTek No.1 glass coverslip dishes Mattek P35G-1.0-14-C Cell Reports 45, 117378, June 23, 2026 25 ..

    Positive Control:

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37
    Article Snippet: Membrane was stripped, re-probed with mouse anti-GAPDH antibody (1:20000, #HRP-60004, ProteinTech Group) overnight at 4°C and incubated with anti-mouse HRP-conjugated antibody (1:10000, #711-035-151, Jackson ImmunoResearch), as above for protein loading control. .. As positive control, total protein extracts were extracted from HEK293T cells transfected with pCMV6-XL4-DAB1 mammalian expression vector (#SC113027, Origene) and 1 μg was loaded on SDS-PAGE gel. .. Graphical representation was carried out using GraphPad Prism, and statistical analysis was performed using IBM SPSS.

    Transfection:

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37
    Article Snippet: Membrane was stripped, re-probed with mouse anti-GAPDH antibody (1:20000, #HRP-60004, ProteinTech Group) overnight at 4°C and incubated with anti-mouse HRP-conjugated antibody (1:10000, #711-035-151, Jackson ImmunoResearch), as above for protein loading control. .. As positive control, total protein extracts were extracted from HEK293T cells transfected with pCMV6-XL4-DAB1 mammalian expression vector (#SC113027, Origene) and 1 μg was loaded on SDS-PAGE gel. .. Graphical representation was carried out using GraphPad Prism, and statistical analysis was performed using IBM SPSS.

    Expressing:

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37
    Article Snippet: Membrane was stripped, re-probed with mouse anti-GAPDH antibody (1:20000, #HRP-60004, ProteinTech Group) overnight at 4°C and incubated with anti-mouse HRP-conjugated antibody (1:10000, #711-035-151, Jackson ImmunoResearch), as above for protein loading control. .. As positive control, total protein extracts were extracted from HEK293T cells transfected with pCMV6-XL4-DAB1 mammalian expression vector (#SC113027, Origene) and 1 μg was loaded on SDS-PAGE gel. .. Graphical representation was carried out using GraphPad Prism, and statistical analysis was performed using IBM SPSS.

    SDS Page:

    Article Title: The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37
    Article Snippet: Membrane was stripped, re-probed with mouse anti-GAPDH antibody (1:20000, #HRP-60004, ProteinTech Group) overnight at 4°C and incubated with anti-mouse HRP-conjugated antibody (1:10000, #711-035-151, Jackson ImmunoResearch), as above for protein loading control. .. As positive control, total protein extracts were extracted from HEK293T cells transfected with pCMV6-XL4-DAB1 mammalian expression vector (#SC113027, Origene) and 1 μg was loaded on SDS-PAGE gel. .. Graphical representation was carried out using GraphPad Prism, and statistical analysis was performed using IBM SPSS.



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