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• 
  @khushiak-47827 күн бұрын

  The vedio is too awesome

• 
  @Haxx-ue6yq8 күн бұрын

  شكراً لقد استفدت كثيراً ❤

• 
  @mustafakouzrite34429 күн бұрын

  Excellent. Please, can you elaborate why the culture has to be 18 to 24 hours old?

• 
  @HardyDx7 күн бұрын

  Aerobic organisms must be taken from an 18 to 24 hour old culture. Organisms lose their catalase activity with age. For slower growing anaerobic organisms, an older (24-72 hours) culture may be acceptable.

• 
  @kimondoDen11 күн бұрын

  Very insightful

• 
  @virensingh-sw5hk13 күн бұрын

  Keep it up gentlemen

• 
  @albertoperez322321 күн бұрын

  can you find borrelia with that?

• 
  @lorettarodman911724 күн бұрын

  I was taught a very different way, always remember that there is more than one way to streak plates everyone! Find what works best for you. Also if you have a bacteria that really sucks at growing on plates from freezer stock I’ve found that not flaming between streaks helps with that

• 
  @christophercatani882025 күн бұрын

  Great great video!

• 
  @ChinenyeOkeke-s6x25 күн бұрын

  How can someone ride of staphylococcus aureus

• 
  @sam65500225 күн бұрын

  why we can not take colonies from MSA ?

• 
  @flowercafe3406Ай бұрын

  Thank you so much. That was perfect!

• 
  @HardyDx24 күн бұрын

  Glad it helped!

• 
  @itanruiz7828Ай бұрын

  Works very great! Thank you.

• 
  @HardyDx24 күн бұрын

  You're welcome!

• 
  @DanTheisenАй бұрын

  Absolutely love this video! The efforts and unmatched generosity that so many fellow employee/owners pour into our community events are simply incredible. Thanks to the volunteers, event leaders, committee leaders, and company executives who make this part of our Culture of Service…to our Community.

• 
  @sahilpathan7894Ай бұрын

  My Bsc Microbiology complete, will I get a job in pharma company. ?

• 
  @jonathanmelo8673Ай бұрын

  No.

• 
  @kunalmistry585629 күн бұрын

  Yes , lots of opportunities

• 
  @shekharchokkam845710 күн бұрын

  Yes u will get job but better u can complete MSc then u will get better opportunity

• 
  @kakoteo315 күн бұрын

  Not immediately, get jobs that get you expirience in USP testing that will raise your chances

• 
  @Bbg-l3hАй бұрын

  THANK

• 
  @MEDIOnAcademyBDАй бұрын

  ❤

• 
  @NiyibugingoValentin-dk7sk2 ай бұрын

  Thank your brother is here with me and I will get it more information

• 
  @mtado49332 ай бұрын

  yeah i fucked it up so badly

• 
  @ry_n0072 ай бұрын

  thank you for saving my ee broski 🙏🙏

• 
  @Faceless_Chat3 ай бұрын

  Very helpful. I have a "unknown bacterium" assignment that starts today. This really helped bc I already forgot you have to sterilize the loop between streaking...

• 
  @sparkleberrypop4 ай бұрын

  Thank you for this video. It is very informative. I hope you can remove the background music or lower the volume down. Thank you

• 
  @HardyDx4 ай бұрын

  Thank you for taking the time to watch our video and for sharing your feedback with us. We truly appreciate your input, and we want you to know that your suggestions will definitely be considered in our future video planning. Regarding the background music volume, we understand your concern. Unfortunately, we are unable to make adjustments to previously posted videos without affecting our current viewership and traffic. However, please know that we are continuously striving to improve the quality of our content based on valuable feedback like yours. Once again, thank you for being a loyal viewer, and we hope you continue to find our videos informative and engaging.

• 
  @joannadevung43584 ай бұрын

  If i accidentally tore the surface of the agar using the loop during streaking, will the bacteria colonies still able to grow?

• 
  @HardyDx2 ай бұрын

  Colonies will still grow, yes. However, it is usually best to restart on a fresh plate as the puncture could lead to difficulties in reading/counting colonies or could cause unwanted areas of heavy growth. Don't worry though! Marring the surface is extremely common, especially in beginners. Keep practicing and you'll be able to do it as if it were nothing!

• 
  @AliyuNanaaishat4 ай бұрын

  Please can I see a video that will teach me more on how to carry out indoor air quality using SDA and PDA

• 
  @miltonkunda89124 ай бұрын

  Why can't I work in one of your labs

• 
  @TheModernVictorian4 ай бұрын

  Sorry, I couldn't watch all the video because of the music, but otherwise what I did see was informative. That kind of cheesy not-even techno-kinda royalty free noise is just too pervasive for some people to focus on what they actually want to hear.

• 
  @thenone69453 ай бұрын

  Quit yapping.

• 
  @Aakif8624 ай бұрын

  Wher you from sir

• 
  @Aakif8624 ай бұрын

  Love from India ❤

• 
  @user-lk9yo4jg3e4 ай бұрын

  kzread.info/dash/bejne/epN8zsyeoJjRZaQ.html

• 
  @user-hm2rl9ef5w4 ай бұрын

  Why did you put the hose inside the autoclave into Erlen?

• 
  @HardyDx4 ай бұрын

  Thank you for your question. The hose is actually a temperature probe. As the video explains the probe can be placed directly into the media (which is in the Erlenmeyer flask aka “Erlen”). As the directions state: “Place the flask of boiling media into an autoclave to sterilize. If your autoclave is equipped with a temperature probe, the temperature probe can be placed directly into the media and the cycle parameters will be based on the readings of the probe.”

• 
  @DoniaNabil-li2fg5 ай бұрын

  Thank you for this interesting video ❤

• 
  @HardyDx4 ай бұрын

  Glad you enjoyed it!

• 
  @user-ly7jy5jr6e5 ай бұрын

  The video on the One step stain is confusing, it says you do not need to use buffer, yet you say to put it in the buffer. Very confusing.

• 
  @PokeSquirtleBlue5 ай бұрын

  Very Informative video comparing the workflow of CompactDry™and Petrifilm™!

• 
  @HardyDx5 ай бұрын

  Glad it was helpful!

• 
  @BAD5RO5 ай бұрын

  Informative

• 
  @M313_16 ай бұрын

  *ثانكيو* 🦦

• 
  @temtuapati6 ай бұрын

  Thank you for the time spent on this video

• 
  @HardyDx5 ай бұрын

  Our pleasure!

• 
  @sumayariza7816 ай бұрын

  So outstanding! Thanks

• 
  @HardyDx6 ай бұрын

  Glad you enjoyed it!

• 
  @ceciliaovansa27386 ай бұрын

  Nice one

• 
  @HardyDx6 ай бұрын

  Thanks for watching

• 
  @ceciliaovansa27386 ай бұрын

  It was nice watching

• 
  @HardyDx6 ай бұрын

  Thanks!

• 
  @Cyan-J-e5u6 ай бұрын

  It's self explanatory and the visuals, helps for easy remembrance. Thanks.

• 
  @HardyDx6 ай бұрын

  You are very welcome. I am glad our video was useful for you.

• 
  @maranada86836 ай бұрын

  EAT MANUKA HONEY!!!!!! YOU CAN eat it straight or mix in a glass with apple cider vinegar!!! Or both!!!

• 
  @metalandwood4u2 күн бұрын

  Did it heal or cure you of this disease ?

• 
  @btsforever39386 ай бұрын

  hey can u tell me how can i prepared slide of water by applying giemsa stain on it for detecting parasite Giardia in water Under the microscope . and also tell me how can i set microscope for it.😩

• 
  @HardyDx6 ай бұрын

  Check out this helpful video on "How to do a hematology stain (Wright-Giemsa stain) Laboratory Tutorial Procedure" kzread.info/dash/bejne/oY5l1M2dmM2wiLQ.html

• 
  @btsforever39386 ай бұрын

  @@HardyDx okay ty✨

• 
  @ZainabLambe-dj5hx6 ай бұрын

  Thank you for the video

• 
  @mehrajgul1316 ай бұрын

  Can this be used in a grade C area as this is a closed system?

• 
  @lordsirmoist15947 ай бұрын

  you know youre entering a career of science and medicine when you get videos like this on your feed

• 
  @nurdiyana92627 ай бұрын

  do you mix the bacteria with nutrient broth or mac farland standard?

• 
  @gulkeshdomun6 ай бұрын

  nutrient broth

• 
  @miaab71437 ай бұрын

  Is it ok to autoclave for 1 hour and a half??

• 
  @ethical_trading01117 ай бұрын

  ❤❤❤

• 
  @KyleZHardyDiagnostics7 ай бұрын

  This is the best Hardy Diagnostics short I've seen so far!

• 
  @PokeSquirtleBlue7 ай бұрын

  This is such a fantastic video. So informative!

• 
  @HardyDx7 ай бұрын

  Glad it was helpful!

• 
  @anycamenzind8 ай бұрын

  Will there be a video available that talks about the microscope and Khoeler illumination? Unfortunately, part of the practical microbiology and laboratory sessions were taken in times of pandemic. Likewise, I would greatly appreciate if you could explain how the UFC colony counter works. Your explanations are great! Thank you 🙌🙌🙌