How to Download and Install Orange5 Software for Memory and Microcontrollers Programming
In the previous article, we introduce the difference between the 2022 new Orange5 Super Pro and Orange5 Plus V1.35. Now we will share the Orange 5 Super Pro V1.35&1.36 software download link and installation guide for new users.
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Do not get confused by Orange pricing. Orange charge separately for the device, the immo software, the airbag software and the radio software, plus a few specials.All this comes with the clone.To compare the two, you must add up all the costs from Orange. There is a very large saving if you buy the clone. But you cannot update it and you have no support from Scorpio. It will suit some people for sure.
New Orange5 Plus clone comes with V1.35 software and full adapters. It adds more new functions than Orange5 and works easier with the USB Dongle. Here share the related software download link and new functions list.
Do not get confused by Orange pricing. Orange charge separately for the device, the immo software, the airbag software and the radio software, plus a few specials.All this comes with the clone.To compare the two, you must add up all the costs from Orange. There is a very large saving if you buy the clone. But you cannot update it and you have no support from Scorpio. It will suit some people for sure. The adapters are poor quality, and for many the hardware does not work. No doubt as time goes by will will see huge threads about how to fix them. The company who makes it does not have a good reputation for quality or support.
2- Copy the OEM Orange 5 software to the computer local disk 3- Disable or uninstall anti-virus software on PC 4- Install Orange5 V1.34 on Windows XP/ WIN7/ WIN8 -to-install-orange5-v1-34-on-windows-xp-win-7-win-8/ NOTE: all above is only for Orange 5 programmer clone
The Orange-5 programmer operates with two kinds of software, one from them is public software and another is pesonal software.Downloaded software update has only the public part.By this if you have a personal parts they must be integrated manually in a new update.
The most simply way is to hold the personal files in some separate place on a computer.After the update downloaded, install it as usually. Next copy the personal files into directory of the programmer.
In order to work the update requires the latest Orange-5 base software. -lk.com/downloads/Orange5/orange5.rarArchive password is same as for the previous version !Mail us with your Orange-5 serial number if you don't have the password.For any problems or questions regarding this update mail us.
1. Built-in update software: Make VVDIProg firmware update timely.2. High-speed USB communication interface: Make software automatically connect.3. Smart operation mode: possible causes of error will be listed4. Reserve ports: For future update.5. Self-test function: Check if the machine works well or not.6. Power supply: Through USB cable, software will automatically prompt if the external USB power supply is needed
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Transverse (a) and longitudinal (b) elastosonographic images of the distal attachment of the fetlock joint capsule (DJC) showing the positioning of the ROIs over the DJC (yellow circle) and the dorsal digital extensor tendon (DDET) (green circle) in one horse of Group S. The top left box shows the elastogram of the transverse (a) and longitudinal (b) scans of the DJC with the superimposed ROI above the DJC (yellow) and DDET (green) in Group S. The bottom left box shows the conventional B-mode image of a transverse and a longitudinal scan of the DJC with the superimposed ROI above the DJC (yellow) and DDET (green). The box at the right side of the image shows the graph produced by the software: the x-axis is time-dependent with green segments indicating the moments of proper pressure and red segments the incorrect ones. The y-axis shows the EI values for the DJC (yellow) and DDET (green). The values of EI are expressed at the top right side of the image. SR, not shown, is then calculated by the software (ROI: region of interest; DJC: distal attachment of the joint capsule; DDET: dorsal digital extensor tendon; EI: Elasticity Index; SR: Strain Ratio)
Transverse (a) and longitudinal (b) elastosonographic images of the distal attachment of the fetlock joint capsule (DJC) showing the positioning of the ROIs over the DJC (yellow circle) and the dorsal digital extensor tendon (DDET) (green circle) in one horse of Group P. The top left box shows the elastogram of the transverse (a) and longitudinal (b) scans of the DJC with the superimposed ROI above the DJC (yellow) and DDET (green) in group P. The bottom left box shows the conventional B-mode image of a transverse and a longitudinal scan of the DJC with the superimposed ROI above the DJC (yellow) and DDET (green). The box at the right side of the image shows the graph produced by the software: the x-axis is time-dependent, with green segments indicating the moments of proper pressure and red segments the incorrect ones. The y-axis shows the EI values for the DJC (yellow) and DDET (green). The values of EI are expressed at the top right side of the image. SR, not shown, is then calculated by the software (ROI: region of interest; DJC: distal insertion of the joint capsule; DDET: dorsal digital extensor tendon; EI: Elasticity Index; SR: Strain Ratio)
Phenotypic analyses of T cells and tumor cells were performed by direct or indirect immunofluorescence on a FACSCalibur cytometer using CellQuest software (BD Biosciences). Briefly, 2 105 cells were stained with Abs (primary and secondary antibodies), washed, fixed with 2% (w/v) paraformaldehyde solution in PBS, and, after washing, analyzed by flow cytometry. For intracellular staining, cells were fixed and permeabilized by 0.1% (w/v) BSA (Sigma-Aldrich) and 0.1% (w/v) saponin (Sigma-Aldrich) solution in PBS (Sigma-Aldrich), stained with the specific Abs (primary and secondary Abs), washed with 0.1% (w/v) BSA (Sigma-Aldrich) and 0.1% (w/v) saponin (Sigma-Aldrich) solution in PBS, and analyzed by flow cytometry.
For monitoring live three-dimensional cultures (over an 18 h period at 37C), stacks of confocal slices were collected every 5 min with a LSM 510 laser-scanning confocal microscope (Carl Zeiss MicroImaging) using a 20 0.75 apochromat plan objective. Z-projection of slices was realized using LSM Image Examiner software (Zeiss). For non-live monitored experiments, one slice (0.38 μm) was collected using a 63 1.4 apochromat plan objective.
For the phagocytosis assay, we used the M4T-derived melanoma cell line M4TD, which is HLA class I negative. M4TD cells were labeled by CMTMR CellTracker probes (5 μM) and exposed to UVB radiation (25 kJ). Necrotic cells were obtained after five serial freeze-thaw cycles. Apoptotic cells and necrotic cells were then collected and cocultured either in a two-dimensional or three-dimensional environment with CMFDA CellTracker-labeled ECs at a ratio of 1:2 for endothelial/apoptotic cells or endothelial/necrotic cells for 24 h. M4E that engulfed apoptotic cells or necrotic cells in a two-dimensional environment were directly sorted on FACSVantage using FACS Diva software (Becton Dickinson). We then tested their recognition by CTL clone M4.48 with a TNF secretion assay.