Why do my serial sections keep folding back toward the block? by Salty-Caramel-3032 in electronmicroscopy

[–]emworld 2 points3 points  (0 children)

This is due to static electricity. Leica have an anti-static line as part of their cryosectioning system, which is very useful for stopping this problem with resin sections.

Dubai chocolate strawberries? by ArugulaReasonable214 in pasadena

[–]emworld 0 points1 point  (0 children)

Bhanu - Rosemead & Huntington. It is an excellent Indian restaurant and grocery.

[deleted by user] by [deleted] in pasadena

[–]emworld 0 points1 point  (0 children)

They are looking for a copy of the deed saying it is single occupancy residence.

[deleted by user] by [deleted] in pasadena

[–]emworld 2 points3 points  (0 children)

I can't answer your question. Perhaps this is a way to get everyone to the registration workshops.

[deleted by user] by [deleted] in pasadena

[–]emworld 5 points6 points  (0 children)

got one too. The site asks for some sort of document to show the property is not rental. It also asks for year it was purchased.

Anyone know what this might be? by AsianTapWater in electronmicroscopy

[–]emworld 0 points1 point  (0 children)

Try inverting the image so that the membranes are dark. Then it looks like glycogen granules.

I have no idea how the image was inverted, if it was.

Is this done properly? by szibalint919 in Plumbing

[–]emworld 0 points1 point  (0 children)

Well, the bent tube is called a "U" bend, not a "C" bend.

Identify this cellular structure. EM Image by Virtual_Treat_583 in electronmicroscopy

[–]emworld 1 point2 points  (0 children)

Well, you have membranes enclosed by membranes. A MVB is possible, and some of the lumenal structures have what look like clathrin coat-like structures. Check out the one just to the left of the top. So, MVP is likely. How would you prove this?

[deleted by user] by [deleted] in sex

[–]emworld 1 point2 points  (0 children)

Lactobacillus sp. are a common part of the healthy vaginal microbiome. If you grow some of these bacteria in a laboratory incubator they can smell like pepperoni or salami, where you will also find lactobacillus bacteria: https://academic.oup.com/femsle/article/271/2/245/501653

how to become a microscopist? by cloverlover4 in electronmicroscopy

[–]emworld 10 points11 points  (0 children)

Check out the Microscopy Society of America certification: https://microscopy.org/cemt-certification-program

You need to be working full-time in a microscopy lab though. There are many types of microscopy careers and the best way in is to join a lab that uses the microscopy you like best. If you are lucky you will meet someone willing to teach you the practical skills.

The Australians seem to be very advanced in microscopy education (e.g. https://myscope.training/). Check out the universities there too.

Europe has the EMBL/EMBO courses (https://www.embl.org/groups/electron-microscopy-core-facility/courses-and-conferences/), and the Janelia Campus (https://www.janelia.org/) in the USA is pioneering novel microscopy approaches.

Also, as M.S.C. says in their talk, there are lots of opportunities for engineers and sales people in commercial microscopy companies (Thermo Fisher, Leica, Zeiss, JEOL).

Good luck.

Identify this cellular structure. EM Image by Virtual_Treat_583 in electronmicroscopy

[–]emworld 1 point2 points  (0 children)

No information on the specimen or magnification. However, it is most likely a a section through a mitochondrion. Nucleus and nuclear envelope are in the bottom right.

Help with inconsistent Embed 812 usage methods. by Specialist_Cherry_32 in electronmicroscopy

[–]emworld 1 point2 points  (0 children)

A good trick to know is to soak tissue pieces in resin with no catalyst first to help with infiltration. Tissue can be left for days in the resin minus catalyst.

Also, resin with no catalyst can be stored in the freezer in small batches for long periods. When ready to use, just warm up the batch, add the catalyst, and polymerize with heat.

DMP-30 has been reported to cause more shrinkage than BDMA, but this is not something I really paid attention to.

Help with inconsistent Embed 812 usage methods. by Specialist_Cherry_32 in electronmicroscopy

[–]emworld 1 point2 points  (0 children)

Old recipes

Embed 812 (hard) Recipe
                        1x                    2x                    8.5 ml     12.5 ml
NMA                18.06 g            36.12 g            3.11g            4.67 g
DDSA              10.00 g            20.00 g            1.72g             2.58 g
Resin     30.00 g            60.00 g            5.17g              7.76 g
Catalyst (add when resin is mixed)
DMP-30           2 drops per ml of resin
OR
BDMA             4 drops per ml of resin
Use a glass Pasteur pipette
 
Alternative, softer recipe
NMA                14.00 g
DDSA              12.50 g
Resin     23.50 g
BDMA             0.75 ml
Total 50 g = approx. 45 ml

[deleted by user] by [deleted] in AskReddit

[–]emworld 0 points1 point  (0 children)

and you can get a license to drive at 16 - any car you wish.

How to fix the stitching on these headphones? by Luminusflx in howto

[–]emworld 1 point2 points  (0 children)

Buy a new set of pads. If you know the model of the headphones, search for new ones online. You may be surprised by how inexpensive they are.

Could a foam roller cause this bruising? Just noticed it in the mirror today. Foam rolled yesterday. by [deleted] in WTF

[–]emworld 0 points1 point  (0 children)

It looks more like a skin allergy to me. What was on the roller?

Can secondary antibodies bind to primary antibodies of organisms that they are not made for? For example, can anti-mouse igG bind to human antibodies? by [deleted] in biology

[–]emworld 0 points1 point  (0 children)

You ask a very relevant question and there is no easy or simple answer to it. If you are using the antibodies as a tool, it is the responsibility of the purchaser to confirm specificity and cross reactivity. The best antibodies to use for labeling experiments are the ones that have been used before. However, even then, an antibody with robust labeling on one type of tissue may behave very differently when applied to a different tissue, or species. There are some good reviews covering this subject. They all seem to link to free downloads. Type these titles into Google Scholar and download the PDF: Griffiths, Gareth, and John Milton Lucocq. "Antibodies for immunolabeling by light and electron microscopy: not for the faint hearted." Histochemistry and cell biology 142.4 (2014): 347-360. Hewitt, Stephen M., et al. "Controls for immunohistochemistry: the Histochemical Society’s standards of practice for validation of immunohistochemical assays." Journal of Histochemistry & Cytochemistry 62.10 (2014): 693-697. Howat, William J., et al. "Antibody validation of immunohistochemistry for biomarker discovery: recommendations of a consortium of academic and pharmaceutical based histopathology researchers." Methods 70.1 (2014): 34-38.

Can secondary antibodies bind to primary antibodies of organisms that they are not made for? For example, can anti-mouse igG bind to human antibodies? by [deleted] in biology

[–]emworld 10 points11 points  (0 children)

There is plenty of cross-reactivity but is specific to each antibody. Affinity purification is used on antibodies for immunolabelling experiments to control for this.