The largest database of trusted experimental protocols

Coreldraw graphics suite x7

Manufactured by Corel
Sourced in Canada

CorelDRAW Graphics Suite X7 is a comprehensive software package designed for professional graphic design, illustration, and photo editing. It provides a range of tools and features for creating and manipulating digital content, including vector graphics, page layout, and image processing capabilities.

Automatically generated - may contain errors

9 protocols using coreldraw graphics suite x7

1

Facial Symmetry Measurement Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
In this method, a picture was taken of the face when the head was completely straight. The picture was analyzed by CorelDRAW Graphics Suite X7 software (Corel Corporation, Ontario, Canada), and two of the following parameters were calculated.
Relative facial size: As shown in Figure 1, the ratio of the distance between the external canthus and the corner of the lips of both face sides, named reference lines, was defined as relative facial size. If the distance between the external canthus and the corner of the lips of both face sides was the same, the face was symmetric based on this parameter.[7 (link),8 (link)][12 (link)] However, when these lines were different, for better comparison of patients, the amount of the longer reference line was divided into the other line and the result was named relative facial size parameter.
Facial angle: As shown in Figure 1, this parameter was measured by calculating the angle between the two following lines; the first line connected two external canthi (line A in Figure 1) and the second line connected the two lips corners (line B in Figure 1). If two lines were parallel, the face was symmetric based on this parameter, however, the presence of an angular difference means facial asymmetry.[7 (link),8 (link)][12 (link)]All quantitative parameters were calculated three times, and the average was reported as a result.
+ Open protocol
+ Expand
2

Rigorous Image Scoring Reliability

Check if the same lab product or an alternative is used in the 5 most similar protocols
All pictures were scored using CorelDRAW Graphics Suite X7 (Corel Corp.). The order of the pictures was randomised and the coder (SH) was blind to condition and phase. After every 50th picture, ten out of these 50 pictures (i.e. 20%) were randomly chosen using the sample function in R and re-scored to assess intra-observer reliability. Additionally, 10% of the total sample were scored by a second coder to test for inter-observer reliability. The second coder was trained with example pictures before coding the sample.
+ Open protocol
+ Expand
3

Statistical Analysis of Experimental Data

Check if the same lab product or an alternative is used in the 5 most similar protocols
The data were analyzed using Statistica, Version 12 (Statsoft Inc., Tulsa, OK, USA, 2013). The assumptions of normality distribution and homogeneity of variance were estimated. Based on the results of the estimation, further analyses were performed using non-parametric tests (the Mann–Whitney U test and the Kruskal Wallis test). The boxplots graphs were created using MATLAB R2009a (The Mathworks, Natick, MA, USA). Spider plots were performed with CorelDRAW®, Graphics Suite X7 (Corel Corporation, Ottawa, ON, Canada). For all analyses, we assumed a significance level of 0.05.
+ Open protocol
+ Expand
4

Visualizing Curcumin Analogs in PANC-1 Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
PANC-1 cells (2 × 105) were plated on µ-Slide 8 Well Glass Bottom dishes (Ibidi®,Martinsried, Germany) in 500 µL media and placed in a humidified incubator at 37° C 5% CO2. After 24 h culturing, detection of curcumin, curcumin analogs (1 µM, 5 min) and ER tracker green (1 µM, 5 min, Thermo Fisher) were performed using Olympus Fluoview FV1000 confocal laser scanning microscope (Olympus Life Science Europa GmbH, Hamburg, Germany ) in triplicates. Microscope configuration was the following: objective: UPLFLN 40× (oil, NA:1.3); dichroic mirror: 20/80, excitation: 405 nm (curcumin analogs), 514 nm (ER tracker); detection range: 425–475 nm (curcumin), 530–630 nm (ER tracker); scanning dimensions: 512 × 512 pixel; sampling speed: 2 µs/pixel; confocal aperture: 182 µm; zoom: 5×; line averaging: 2×. Curcumin analogs and ER tracker green images were pseudocolored as cyan and green, respectively. Transmitted light images were also captured with 514 nm laser and paired with each fluorescence image. ER tracker green imaging was performed using 514 nm laser instead of 488 nm laser to minimize channel crosstalk. Composite images were prepared using CorelDraw® Graphics Suite X7 (Corel, Ottawa, Canada).
+ Open protocol
+ Expand
5

Multicolor Fluorescence Imaging of Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human U2OS and HEK293 cells were seeded in 8-well chamber slides (1x104 cell/well) in complete DMEM and transfected next day with 0.25 μg of CFP and YFP fusion plasmids using Turbofect transfection reagent (Fermentas, Lithuania) as previously described [9 (link)]. Confocal laser scanning microscopy was performed using Olympus Fluoview FV1000 laser scanning microscope (Olympus Life Science Europa GmbH, Hamburg, Germany). Microscope configuration was the following: objective lens UPLSAPO 40x (oil, NA 1.3); sampling speed: 8μs/pixel; scanning mode: sequential unidirectional; excitation: 458 nm (CFP) and 515 nm (YFP); laser transmissivity: 30% and 10% were used for CFP and YFP, respectively; main dichroic beamsplitter: DM458/515, intermediate dichroic beamsplitter: SDM 510; CFP was detected between 470–520 nm and YFP was detected between 520–570 nm. Differential interference contrast (DIC) or standard transmission images were captured with 515 nm laser line. Composite images were prepared using CorelDraw Graphics Suite X7 (Corel).
+ Open protocol
+ Expand
6

Morphological Characterization of Turkish Beetles

Check if the same lab product or an alternative is used in the 5 most similar protocols
The field trips of this study were made in different provinces of Turkey between 2010 and 2019 (Figure 1). Specimens were collected by hand and pitfall traps. Photographs of the primary and secondary characters were taken with a Zeiss Axiocam ERC5s digital camera connected to a Stemi 508 (Zeiss Germany) stereomicroscope. Helicon Focus 6.0.18 image stacking software was used to combine photographs which were taken in different focal planes. CorelDRAW Graphics Suite X7 was used to create the plates and edit photographic images. Google Earth Pro was used to create the maps. Hanley & Ashe (2003) were followed for dissection techniques. Terminology for the body parts, aedeagus and spermatheca structures follows Assing (2005) . The material is deposited in AZMM (Alaşehir Zoological Museum, Manisa, Turkey) of Manisa Celal Bayar University.
The following abbreviations are used for the measurements: AL, length of antenna; AW, maximal width of abdomen; EL, length of elytra from apex of scutellum to posterior margin at suture; EW, width of elytra; HL, head length from anterior margin of clypeus to posterior margin of head; HW, head width (including eyes); ML, length of aedeagus from apex of ventral process to base; PL, length of pronotum along median line; PW, maximal width of pronotum; TaL, length of metatarsus; TiL, length of metatibia; and TL, total length.
+ Open protocol
+ Expand
7

Morphological Study of Staphylinidae in Western Anatolia

Check if the same lab product or an alternative is used in the 5 most similar protocols
The material studied was collected using aspirators in Aydın, Balıkesir, Denizli, İzmir, Kütahya, Manisa, Muğla Provinces of western Anatolia between 2014 and 2016. Dissection techniques followed that of Hanley & Ashe (2003) . The morphological studies were carried out by a Stemi 508 (Zeiss Oberkochen, Germany) stereomicroscope. Photographs were taken with a Zeiss Axiocam ERC5s digital camera. Adobe Photoshop 2020 was used for focus stacking. CorelDRAW Graphics Suite X7 was used for editing photographs. Google Earth Pro was used to create the map. Primary and secondary sexual characters of the species are described following the terminology of Assing (2006; 2010) . Head length was measured from the anterior margin of the frons to the posterior margin of the head, length of the pronotum was measured along the median line; elytral length was measured along suture from the apex of the scutellum to the posterior margin; the length of the median lobe of the aedeagus was measured from the apex of the ventral process to the base of the capsule. The material is deposited in Alaşehir Zoological Museum, Manisa, Turkey (AZMM).
+ Open protocol
+ Expand
8

Visualizing Maize Apical Meristem with Fluorescence Microscopy

Check if the same lab product or an alternative is used in the 5 most similar protocols
Fluorescent oligonucleotide-injected apical meristem regions of 6-day-old hand sectioned maize seedlings were imaged using Leica SP5 laser scanning confocal microscope (Leica Microsystems GmbH, Wetzlar, Germany) either by directly layering intact potted plants' leaf over the immersion objective using a coverslip-bottom Petri dish (Fodor and Ayaydin 2018) or by excision of the leaf and mounting on 24 × 50 mm coverslip. For chlorophyll imaging, 543-nm laser and a detection range of 650-750 nm were used. For cell wall autofluorescence, 405-nm laser excitation and 415-530-nm emission range were used. Macroscopic leaf images were captured using Samsung Galaxy Note 8 mobile phone camera (Samsung Electronics, Seoul, South Korea). Plot profile measurement of selected rectangular areas was performed using Fiji software (Schindelin et al. 2012) . Exported intensity values of plot profiles were used to plot the charts in Microsoft Excel 2010 (Microsoft, Redmond, WA, USA). Composite images were prepared using CorelDraw Graphics Suite X7 (Corel Corporation, Ottawa, Canada).
+ Open protocol
+ Expand
9

Fluorescence Microscopy Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
For fluorescence stereo microscopy screening, an Olympus SZX12 stereo microscope was used with GFP filter set. Confocal laser scanning microscopy was performed in an Olympus Fluoview FV1000 confocal laser scanning microscope. Microscope configuration was the following: objective lenses: UPLSAPO 20x (dry, NA: 0.75), UPLFLN 40x (oil, NA: 1.3); excitation lasers: 488 nm and 543 nm; GFP and fluorescein diacetate (FDA)
(1 µg/ml, 5 min) were detected between 505-530 nm, propidium iodide (PI) (1 µg/ml, 5 min) was detected between 570-670 nm using spectral detectors. Transmitted light (bright field) images were captured with 488 nm laser line. Composite images were prepared using ImageJ software (National Institutes of Health, USA, version 1.41) and CorelDraw Graphics Suite X7 (Corel).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!