morange sequence (TaKaRa)
Structured Review

Morange Sequence, supplied by TaKaRa, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pmorange2+vector/pmc08079664-285-4-9?v=TaKaRa
Average 93 stars, based on 3 article reviews
Images
1) Product Images from "Combining electrophysiology and optogenetics for functional screening of pyramidal neurons in the mouse prefrontal cortex"
Article Title: Combining electrophysiology and optogenetics for functional screening of pyramidal neurons in the mouse prefrontal cortex
Journal: STAR Protocols
doi: 10.1016/j.xpro.2021.100469
Figure Legend Snippet: Experimental images from patch-clamp recording using LED light (A) Patch-clamp setup for electrophysiological experiments. (B) Amplifier for the recording (upper) and patch pipettes made from glass capillaries using a puller machine (lower). (C) Blue light shining during the experiments to confirm the fluorescent expression of mOrange or GFP. (D) Images of GFP-negative control and GFP-positive knockdown neurons through DIC microscope during the experiment. The upper neuron that is surrounded by the black circle is the control neuron and white cells mean the GFP-positive neurons (lower black circle). Scale, 50 μm. (E) PC screen on which the PATCHMASTER program is running to record synaptic currents evoked by optogenetic stimulation. (F) Scheme of possible neuron pairs in the electroporated mPFC.
Techniques Used: Patch Clamp, Expressing, Negative Control, Knockdown, Microscopy, Control
Figure Legend Snippet: Summary of plasmids in this protocol
Techniques Used: Plasmid Preparation, Control, Sequencing
Figure Legend Snippet: Validation of efficiency of the KD miRNA in HEK 293T cells (A) Illustration of workflow to evaluate the efficiency of the KD-miRNA vector compared to the Scr-miRNA vector for targeted genes in HEK293T cells. The illustration was made by BioRender. WT: wildtype, Res: rescue. (B) Representative images of the GFP and mOrange from the transfected HEK293T cells in each condition. Scale, 100 μm.
Techniques Used: Biomarker Discovery, Plasmid Preparation, Transfection
Figure Legend Snippet: Sparsely-labeled opsin (Chronos with GFP) in the miRNA expressing neurons in the electroporated neurons (A–C) Representative Images of fluorescent expression of Chronos with GFP (A) and, KD miRNAs with mOrange (B), and the merge image showing the double-positive neurons (C). Scale, 500 μm. (D) Scheme of the patch-clamp recording using optogenetic stimulation. (E) Representative traces of optogenetically induced EPSCs from a non-fluorescent control neuron.
Techniques Used: Labeling, Expressing, Patch Clamp, Control
Figure Legend Snippet: Summary for comparison of pairs of pyramidal neurons in paired-pulse stimulation
Techniques Used: Comparison, Plasmid Preparation, Expressing
Figure Legend Snippet: mOrange-sparse labeling for spine analysis (A) Images of the sparse labeling of GFP vector for the miRNA (left), mOrange vector (middle) as a reporter to label the individual neuron sparsely, and merge (right). Scale, 50 μm. (B) Representative images of dendrites from the mOrange-labeled neurons. Scale, 5 μm.
Techniques Used: Labeling, Plasmid Preparation
Figure Legend Snippet:
Techniques Used: Recombinant, Mutagenesis, Transfection, Blocking Assay, Expressing, Plasmid Preparation, DNA Purification, cDNA Synthesis, Ligation, Software, In Utero, Electroporation, Microscopy

