File:Trüpsiini kristallid polariseeritud valguses.jpg
From Wikimedia Commons, the free media repository
Jump to navigation
Jump to search
Size of this preview: 544 × 599 pixels. Other resolutions: 218 × 240 pixels | 436 × 480 pixels | 697 × 768 pixels | 929 × 1,024 pixels | 1,865 × 2,055 pixels.
Original file (1,865 × 2,055 pixels, file size: 1.28 MB, MIME type: image/jpeg)
File information
Structured data
Captions
Summary
[edit]DescriptionTrüpsiini kristallid polariseeritud valguses.jpg |
English: Crystals of enzyme trypsin under Nikon SMZ800 microscope using polarizing lens. Polarizer is a simple solution to distinguish protein crystals from salt crsytals due to their optical differences, saving time and money not measuring salt crystals in diffractometer. Crystals were grown in the presence of benzamidine at room temperature and using seeding technique for obtaining crystals of better quality.
Eesti: Trüpsiini kristallid Nikon SMZ800 mikroskoobi all läbi polariseeriva filtri. Polariseeriv filter annab kristallimise teaduses lihtsa võimaluse eristada valgu kristalli soolakristallist, kuna valgu kristall on valguse suhtes enamikel juhtudel anisotroopne, soolakristallid tihti mitte. Soolakristalli mõõtmine difraktomeetri või sünkrotroniga oleks aga aja ja ressursside kulu. Trüpsiin on oluline ensüüm seedeelundite töös, lagundades valke väiksemateks ühikuteks. Kristallid kasvatati 22 kraadi Celsiuse juures bensamidiini (trüpsiini inhibiitor, soodustades kristallide ning korrektsema kristallstruktuuri teket) juuresolekul ning piisava suurusega kristallide saamiseks kasutati nn külvamistehnikat (seeding). Kristallimisel varieeriti pH ning soola (ammooniumsulfaat) kontsentratsiooni, pildil on parima kvaliteediga kristallid kõigi katsetatud tingimuste hulgast ning sobilikud kristallstruktuuri mõõtmiseks difraktomeetris. Pilt on tehtud nutitelefoniga Samsung Galaxy SII(kaamerasilma suurus on sobilik mikroskoobi okulaari avaga) Tromsø Ülikooli Norstruct laboris. |
Date | |
Source | Own work |
Author | Taavi Ivan |
This image was uploaded as part of Estonian Science Photo Competition.
|
Licensing
[edit]I, the copyright holder of this work, hereby publish it under the following license:
This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license.
- You are free:
- to share – to copy, distribute and transmit the work
- to remix – to adapt the work
- Under the following conditions:
- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
- share alike – If you remix, transform, or build upon the material, you must distribute your contributions under the same or compatible license as the original.
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 17:22, 18 October 2012 | 1,865 × 2,055 (1.28 MB) | Taavi.Ivan (talk | contribs) | {{Information |Description ={{en|1=Crystals of enzyme trypsin under Nikon SMZ800 microscope using polarizing lens. Polarizer is a simple solution to distinguish protein crystals from salt crsytals due to their optical differences, saving time and mo... |
You cannot overwrite this file.
File usage on Commons
There are no pages that use this file.
File usage on other wikis
The following other wikis use this file:
- Usage on et.wikipedia.org
- Usage on ro.wikipedia.org
Metadata
This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. The timestamp is only as accurate as the clock in the camera, and it may be completely wrong.
Camera manufacturer | SAMSUNG |
---|---|
Camera model | GT-I9100 |
Exposure time | 1/33 sec (0.03030303030303) |
F-number | f/2.65 |
ISO speed rating | 125 |
Date and time of data generation | 10:21, 17 September 2012 |
Lens focal length | 4.03 mm |
Width | 3,264 px |
Height | 2,448 px |
Orientation | Rotated 90° CCW |
Software used | I9100XWLPX |
File change date and time | 10:21, 17 September 2012 |
Y and C positioning | Centered |
Exposure Program | Aperture priority |
Exif version | 2.2 |
Date and time of digitizing | 10:21, 17 September 2012 |
APEX shutter speed | 5.05 |
APEX aperture | 2.81 |
APEX brightness | 2.46 |
APEX exposure bias | 0 |
Maximum land aperture | 2.81 APEX (f/2.65) |
Metering mode | Center weighted average |
Flash | Flash did not fire, compulsory flash suppression |
DateTimeOriginal subseconds | 00 |
DateTimeDigitized subseconds | 00 |
Supported Flashpix version | 1 |
Color space | sRGB |
Exposure mode | Auto exposure |
White balance | Auto white balance |
Scene capture type | Standard |
Unique image ID | SBEF02 |
Hidden categories: