#labproject

[beebeebrojan]

BERT AND GLO Prenuptial Photo: Lab Project Studio #Labproject #Labprojectphoto #weddingphoto #weddingday #weddingbells #wedding #weddingphotography #weddinginvogue #weddingphilippines #weddingtime #urdanetawedding #prenupshoot #prenup #bacacayprenup #weddingmagazine

[chefsalvatorecuomo111]

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A post shared by Salvatore Cuomo (@chef_salvatore_cuomo)

Where to choose the right place to build a food laboratory @labo3680 ?? Our indispensable base in the kitchen is water so we chose this place, perhaps it could also be the reason why only in this place unique dishes will be experimented & not copyable in other location. Water is the source of everything. . . . . #lab3680 #labproject #japan #water #foodlabo #teamsalvatorecuomo #chefsalvatorecuomo #water #kyushu #life #chefslife #teamlab3680 https://www.instagram.com/p/CCuOm07FPHs/?igshid=15r3lulg89xjv

[dataviz2018spring]

erp2151

[asereneserendipity-blog]

Lab Project Week 2

My supervisor is gonna be away for a few weeks, starting from 25/4 - my second week in the lab! I imagined things were gonna be chaotic, because 1. I don’t have that much experience in doing the things that I’m supposed to do; 2. The people who are more experienced are in the holiday mood too (one is enjoying life in Portugal and another left early daily and starts to enjoy her life in Paris right now); 3. My Thai colleague is only a lil’ bit less clueless than I am and most of the time we need to rely on our supervisor’s guidance; and 4. My supervisor was gonna attend a conference in Indonesia which is 6 hours ahead - meaning that if we have anything urgent to report / ask for help we can’t get reply in time!

Luckily, the first week without my supervisor’s supervision went ok. Shit happened (which is something that happens in the lab anyway) and I got to fix them / at least made them less worse. There came to a point where I had to improvise stuff and did it before getting a green light from my supervisor (he’s known for being a lil’ bit slow in responding to emails, apparently. And who can blame him for the late replies - he’s in a different time zone anyway!) and I was so glad to receive an email from him afterwards saying that what I did was correct! #BornToBeScientist

Just to summarise what went wrong during week 2:

1. My cells grow really slow - can’t say that it’s something that gone wrong cause’ as long as the cells are healthy and are not infected *touch wood* then I’ll be fine. 

It’s just that since they are growing so slow that I have to wait for them to reach a certain confluence, I can’t harvest them (for SDS-PAGE) and seed them on coverslips (for IFA) yet. Which slows down my progress altogether urgh.

Lesson learned: I can be quite impatient when it comes to lab work - I need to see results and I need to keep my head and hands busy all the time. But because lab works are usually continuous ie you have to complete the previous step in order to carry out the later step, the former can easily affect downstream works. There are also incredibly lots of protocols with waiting times - some 5 mins, some 1 hour, some overnight - which have both their pros and cons. Pros: If you plan it carefully you only have to work half-day (only to carry on the downstream work the day after). Cons: If you screw up a crucial step (let’s hope it doesn’t ever happen to whoever works in a lab) you might need to start it all over again and it might take up a whole freaking day. And this leads to...

2. I screwed up my second gel by staining it with Coomassie Blue. And I only realised it when I got back home. While talking with my parents. As I was about to record my lab book and started to refer to protocols. And I read the protocols listed under Western blot. And it came across to me like a super bright meteor shower rains upon Earth, that I FREAKING SHOULDN’T STAIN THE GEL IF I WERE TO PERFORM WESTERN BLOT. Idiot. I was too confident after the gel done running. It felt so natural to pour the blue staining solution into the plastic container with my gel in. Only to realise (after placing the gel on a rocker to let it stain overnight) after a couple of hours later that I’D DONE SOMETHING SO TERRIBLY WRONG I felt like apologising to the gel for mistreating it. 

Lesson learned: If you accidentally stain your gel that you were supposed to do Western blot with, just destain it completely (it’s a trick - you’d have to change the destain solution every hour until you can’t see the bands [or something along that line]). When Lisa told me that I thought “Thank God, I don’t need to re-do my gel afterall. But guess what - it took ages for the gel to be completely destained that I decided to just run a new gel instead. It only took me less than 2 hours to run a new gel and get the transparent (as it’s supposed to be before staining) baby. But before running the gel, I faced some problems...

3. Those freaking chipped glass plates made my gel (before it settled) leaked. Damn I made 3 gels and ALL OF THEM LEAKED. D: I was so frustrated that in the end I couldn’t be bothered to make a new gel anymore I used the one with the least leak. And it run ok, so I guess the leak didn’t affect the running much. But I won’t know if it does have any effect on protein separation until the X-ray film (which the membrane is exposed to) is developed. Let’s hope my first Western blot attempt is a success *fingers crossed*!

4. The doxycycline that I added to my NS1 cultures was in the wrong concentration! My Thai colleague aliquoted the solution for me which is really sweet of her, but she wrote the wrong concentration on the tube. And both of us added one tenth of the required concentration to our cell culture. She realised it after checking with the stock and emailed our supervisor about this, and thank god he said that it was fine, as long as we stick to the required concentration the next time we split them. Phew!

5. Apparently I can split the NS1 and Rep cells at 1:2 or 1:3, instead of the 1:12 and 1:24 that I’ve been doing. No wonder my Thai colleague’s cells are growing at a much faster rate than mine (she was splitting the cells at 1:3)! I didn’t know that we can increase the cell ratio until this morning (my supervisor emailed us) and I immediately split my cells according to my judgement afterwards - some I need them to grow faster, and some slower (to accommodate the long weekend). If only I knew it earlier, I could have harvested and seeded my cells already! :<

I’m a person who saves the best for last. That said, I received a lot of compliments from my supervisor and colleagues. My first gel turned out to be really good, the bands were well-defined and I didn’t break it. That gave me confidence in running gels (I need confidence as I’ll be doing electrophoresis for god knows how many times for my project zzz). I did my first gel-membrane transfer and it went well (without supervision and guidance!)! At least at the end of the transfer my gel turned transparent, indicating that all proteins had been transferred onto the membrane (although whether or not it is a good transfer depends on the protein detection, which [hopefully] I will be able to perform next week).

My supervisor also likes it when I update him on my progress and my plans. I guess being active in reporting progress leaves a good impression as supervisors don’t have to ask students for their progress. Otherwise it would seem as if the supervisors are nannies and students the babies, which doesn’t really sound good - we are graduate students and/or adults, for whatever sake! 

Although I didn’t get to achieve Stage 1 of my project (as suggested by my supervisor) by week 2, I guess I did pretty alright / didn’t screw up that much. My supervisor mentioned that it’s fine to take things slowly - I guess he can sense the impatience in me - so long as I have some decent results to show to him when he comes back, instead of rushing things and get none done with. Which I kinda agree. After all, lab work is (mostly) result-oriented. No one really cares how much work you did / how much effort you put into, so long as you have (hypothesised) results to show. 

I really enjoy doing lab works. I am much more convinced that I’ll survive the years working in the lab when I start doing my PhD. And I really love the idea of me spending time working towards achieving something that I’ve been dreaming about. 

[snipersnapper]

#kitchenscience #kitchensciencelab :D yay! we made it through our first #homeschoolscienceproject #labproject on the the unit for the 'scientific process', then 'designing an experiment' This one is for my #7thgrader, but the #5thgrader learns, too. We were investigating the effects of different temperatures of water from almost boiling (90deg) to iced water (-15deg) on the sprouting of mongo seeds. We found out 80deg water helped them sprout fastest! Lab reports to be done next. Just so things don't go to waste, we've planted the seeds to grow plants that will be the 5th grader's experiment: the effects of different fertilizer concentrations on plant growth. #exciting #kaaliwlang :D #homeschooling #homeschoollife

[mx-phoenix-nixon]

My first clay model from last week with #LABproject #ProperJob

[junkieforjungkookie]

In the lab waiting to do the next part of my experiment. Can't wait to go home and get pancakes. #bored #labproject #hungry

[beebeebrojan]

Ah Hamra Tower Kuwait #Urban #buildings #kuwait #kuwaitcity #kuwaitbuilding #kuwaitarchitecturalphotography #kuwaitarchitecture #urbanphotography #blackandwhitephotography #streetphotography #blackandwhite #kuwait2020 #blackwork #photooftheday #labproject #labprojectphotography #fujifilm #fujifilmxt20 #fujifilm_global #fujifilm_kuwait #fujifilm_xseries #fujifilmphotography #pinayphotographer #albayphotographer #expatphotographer #alshaheedpark https://www.instagram.com/p/B6yxYG2ArAv/?igshid=uguqsch0yruo

[everythingdippedingold]

Touch your toes #neon #AmericanApparel #LABproject #QueenswayPlaza #Admiralty #HongKong (at LAB CONCEPT Queensway Plaza)

[labprojectltd]

#labproject #givenchy #saintlaurentparis #cheistianlouboutin

[cassleah]

Am I #Arora yet? #jellyfish #marinebiomechanics #labproject #bioluminescene

[asereneserendipity-blog]

Lab Project Week 1

After having nothing to do (except for two assignments which were not that bad) for 10 weeks (it doesn’t seem like a very long time but trust me, time pass really slowly if you’ve got nothing better to do than watching shows. And eating, of course), I FINALLY STARTED MY LAB PROJECT ON APR 18TH!

:D

First impression

What a joyous moment it was when I stepped into the lab with one of the technician fellows who was gonna conduct my lab induction. Although the lab is just situated in our own Biomedical Science building (not as fancy as my cousin’s project cause’ she got to do her project in liaison with NHS as she had to obtain patient samples, thus she got to receive another access card with NHS logo on it which I was so jealous of), I was thrilled cause’ it was my first time entering an ACGM Level 2 lab - a restricted lab that only permitted workers can enter. How cool does that sound!?  

First tries

Of course, working with cell culture (stably expressing viral replicon) means that I’ve got some forms to fill up and training to go through, but that’s ok, cause’ really, I’ve always wanted to do cell culture! I remember that when we had lectures on cell culture I thought that it’s going to be difficult to perform, plus the red DMEM (media) and the uniquely-shaped T75 flask aren’t common materials that you’d see in a normal lab. Turns out, performing cell culture (or cell passaging) is easy enough! On my third attempt I can already perform it without referring to the protocol! *self pat-on-shoulder* Cell culture was the first technique I learn in this lab, and it is the basic of my lab project, really, cause’ I’ll be growing my own cell line samples and all downstream works are based on the cells that I grow. 

Another technique that I’ve always wanted to learn is IFA, and I finally got to try it out on Fri (Apr 22th). Honestly, it’s not as fancy and as cool as I’d imagine it to be - cause’ really, it’s just seeding the cells on coverslip > fixing > permeabilising > blocking unspecific protein interactions > incubating with primary antibodies > incubating with secondary antibodies > immunostaining > examining under IF microscope. Every reagent is colourless (except for the sec. antibodies & staining reagent) and it does not have a single magical moment. AT ALL. Which kinda disappoints me, really, cause’ you’d think that for such a cool visualising technique the method behind must be really amazing, But nah. It’s just as ordinary as the methods used in other techniques. :/

First acquaintances 

In our lab, there’s currently a post-doc (really friendly and helpful, knowledgeable; basically the ‘nanny’ of our lab. A really kind one), 5 PhD students (2 are in the process of writing up their papers; 1 is kind and helpful as well, but seems to be a lil’ bit awkward / shy; 1 is really unfriendly, doesn’t speak much (doesn’t even greet me, let alone talk to me zzz), seems to only minding her own business; 1 is very helpful, especially because the kind of stuff that we are working on are roughly the same for the time being, so she’s been guiding me and providing useful information related to lab works - she’s like my mentor and I’m grateful that I have a senior to refer to whenever I have doubt in any aspect of the work that I’ll be doing, cause’ if not I think I’d still be very blur and unsure of what I was gonna do). Next week or the week after there’ll be another PhD student joining us, making our lab a 10-member (plus 2 supervisors) happy family (well maybe not the PhD student who is always pulling a long face but... I’m just talking about the majority here). 

Side-notes 

Although I won’t actually be dealing with infectious agents (I’ll just be using DENV replicon, which is non-infectious) but the thought of me finally advancing into virology is really exciting. With all the shadowing and practices that I’ve been doing during the first week, I’m sure that I’ve slowly gotten the hang of it. Mistakes were made but I’ve learned and gained experience. I won’t be defeated by what I did wrong or did not so well because it’s from those imperfections that I learn to improve my skills. Be it cell culture, SDS-PAGE, WB, or IFA, I’m sure with practice and patience I would be able to perform the experiments with confidence and hopefully that’ll lead to obtaining the optimum results for my project. I really hope that the results of my project would contribute, no matter how insignificant, to constructing a larger, clearer, and better picture of the scientific world. 

At least my passion ignites a spark within my heart that is gonna burn brighter. A spark that is fuelled by my thirst for knowledge. A spark that acts as a guide in my future undertakings. 

[ivanolita]

LABproject

LABproject is an online platform that acts as an extension of Nick Ballon's photographic book Ezekiel 36:36, released on August 1st 2013. Ballon's fascination and personal connection with Bolivia is brought to life with his documentation of Lloyd Aéreo Boliviano (LAB), one of the world's oldest surviving airlines which is currently under threat of closure. LABproject presents the history and back-story of LAB and its community. The story is in many ways the story of Bolivia and its people: people perpetually looking towards a promised future which never seems to arrive.

[mx-phoenix-nixon]

Last day of #LABproject #ProperJob

[daisyeileen-blog]

Oh you need some icy hot?i gotchu!lol #pharmacytech #labproject

[beebeebrojan]

ISHIAYAGREY CAFE MENU By @beebrojan of #LabProjectDesign #labproject With the help of @addie_nava and @akoinisicells , thank you guys. #coffeeshopmenu #labProjectphotography #coffeelabproject (at Philippine International Convention Center) https://www.instagram.com/p/Bo2t2_8n4w7/?utm_source=ig_tumblr_share&igshid=14lva087vzfez