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Sylvie Le Guyader on
URL: http://confocal-microscopy-list.275.s1.nabble.com/comparison-of-lasers-for-MPM-tp7582206p7582222.html
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Hi again
I agree that the service quality is area dependent and we are super happy with our Swedish Coherent service.
However the policy that the customer pays for shipping the laser back comes from Coherent so i would strongly advise scrutinizing the warranty conditions and asking about this if nothing is specified.
We paid 3000€ to ship a defective laser despite a full service contract last year.
I do not know if SP applies the same policy.
Sylvie
On 18 jun 2014, at 23:57, "Armstrong, Brian" <
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Hi All, our experience with Coherent is quite the opposite. When our Chameleon Ultra was failing after 2500hrs, Coherent shipped the new LASER and we swapped them so that we did not lose even a single day of function. I think that we have done this three times now. Each time it has been a smooth transition. Several years ago they replaced a Chameleon 210 with an Ultra without charge. I would buy only Coherent for this very reason.
With many products the service seems to vary depending upon the area and service personnel.
Our experiences may be confined to Southern California but I believe Coherent company policies are customer oriented.
Cheers,
Brian D Armstrong PhD
Associate Research Professor
Director, Light Microscopy Core
Beckman Research Institute
City of Hope
Dept of Neuroscience
1450 E Duarte Rd
Duarte, CA 91010
626-256-4673 x62872
-----Original Message-----
From: Confocal Microscopy List [mailto:
[hidden email]] On Behalf Of Henthorn, Jim C. (HSC)
Sent: Wednesday, June 18, 2014 7:34 AM
To:
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Subject: Re: comparison of lasers for MPM
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Pam,
I defiantly would not consider Coherent, since we have a Chameleon XR that died with 334 head hours and our only option is to send it to Scotland for repair for $35,000. I was told that the service with the Mai Tai is much better.
Good luck,
Jim Henthorn
Flow and Image Cytometry Lab
975 NE 10th Street BRC 1317
Stanton L Young Biomedical Research Building
Oklahoma City, OK 73104
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http://research.ouhsc.edu/core-facilities/On Jun 18, 2014, at 2:50 AM, Sylvie Le Guyader <
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Hi Pam
If you are into second and third harmonic generation, it can be useful to design the system so that you can split your TiSa before you pump it to higher wavelength. This way you get one line at 900-1000 nm to excite your fluorophore and one line at 1200-1300 for THG to visualize the tissue structure.
Both SP DeepSee and Coherent TiSa/OPO can be split that way but the SP DeepSee delivers a fixed lower wavelength (1040nm which works for RFPs) and a tunable longer wavelength (690-1300nm) whereas in the Coherent system, both wavelength can be tuned (more flexible but more expensive).
The question is then very much if you want to image second and third harmonics.
If you do not need to THG, my understanding is that the SP and Coherent lasers are equivalent although I have only played with the Coherent Ultra II and the question is then if you want some compensation or not as Craig mentioned.
Med vänlig hälsning / Best regards
Sylvie
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Karolinska Institutet
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office: +46 (0) 8 5248 1107
LCI room 1: +46 (0) 8 5248 1172
LCI room 2: +46 (0) 8 5248 3542
mobile: +46 (0) 73 733 5008
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Sent: 18 June 2014 08:48
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Subject: Re: comparison of lasers for MPM
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Excellent point, Craig! I¹m running a core facility, so I have a lot of different users
with different applications. So I guess from that standpoint, I¹m looking for
thoughts on how the systems compare in range of use, ease of use, and reliability.
Because you are right, each user will have a different application!
Dr Pamela A. Young
| Light and Optical Microscopist
Australian Centre for Microscopy & Microanalysis
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On 18/06/2014 12:55 pm, "Craig Brideau" <
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You are asking a bit of an 'apples vs. oranges' question here, in that
different lasers with different accessories achieve different functions.
Different lasers will be appropriate or inappropriate, depending on the
type of imaging you want to do and the types of fluorophores you want
to work with.
I always start by asking the user what non-linear imaging they want to do.
The usual answer is 2-photon, but some also want second harmonic
generation capability (SHG), and some want higher-order 3-photon
imaging, although this is pretty rare. This question gives clues as to
what pulse width and tuning range the user may require.
The next is what sort of tissues the user wants to image, and how deep
they want to go. If they want to go very deep, this indicates that
longer wavelength tuning ranges are appropriate, as well as dispersion
control with shorter pulse widths, pointing to OPO or just a
long-tuning Ti:Saph and pulse compression accessories. For relatively
shallower imaging on not particularly scattering samples, these
measures are not necessary.
Then I ask what sort of fluorophores the user is used to working with,
and which ones they plan to use. This will help nail down exactly what
excitation wavelengths will be necessary, indicating what sort of
tuning range will be necessary out of the laser, and whether or not an
OPO will be needed. For multiple fluorophores it is important to
determine if all of them can reasonably be excited by a single
wavelength, or whether a second wavelength would be needed, which again
points to an OPO for this situation. If the dyes the user wants will
all work adequately with a single wavelength than just a basic laser is
sufficient.
Finally, the experience level of the user, and whether or not the
system will be a 'core' system for multiple users, influences how
user-friendly and turnkey the system and its accessories need to be.
These are not the only considerations, but I hope it gives you some
idea of the thought processes that go towards selecting a laser.
Craig Brideau
On Tue, Jun 17, 2014 at 8:31 PM, Pamela Young
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Hello List,
Has anyone done any comparisons of MPM lasers? Most of my experience
has been with various versions of the MaiTai and the InSight DeepSee
(and of course many much older lasers). So if you have thoughts on
how these systems compare to the Chameleon and OPO, I would love your
thoughts.
Thanks,
Pam
Dr Pamela A. Young | Light and Optical Microscopist Australian Centre
for Microscopy & Microanalysis
THE UNIVERSITY OF SYDNEY
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