StatLab ’s Post

Understanding the difference between mitosis and meiosis can feel like a huge task. But here’s the truth—it's actually a lot simpler than you think! Once you grasp a few key ideas, comparing these two processes won’t just be easy, it’ll be fun. Whether you're prepping for a biology exam or just trying to understand what happens inside our cells, you’re in the right place. In this blog, we’ll break down mitosis and meiosis so clearly that by the end, you’ll be a pro at telling them apart. Let’s dive in! https://wix.to/6jGjOdb

Register now for this Nature webinar with Xuan Zhang from Cincinatti Children's Hospital as he talks about "Defining the bone marrow atlas with high-dimensional biology via a novel CITE-seq workflow". Learn how Curiox laminar wash technology helped to improve this workflow. https://lnkd.in/gj_qqG-B #flowcytometry, #laminarwash, #ScienceAdvancements, #sampleprep, #CITEseq, #highdimensionalbiology

📰 Our latest newsletter just dropped! 📰 * Exclusive Reseller collaborations * Brand New OEM Network * The pE-400max in action * Unlocking spatial biology applications with the help of Kromnigon ... Did you get it? No..? That must mean you're not subscribed! Never miss out on the latest updates ever again. Stay in the loop and subscribe to our #newsletter today! 📨✨ 👉 https://lnkd.in/eHYCRPnA #FluorescenceMicroscopy #cellbiology #lifesciences #lablife #subscribe #microscopy

Hope you can join me tomorrow and hear about the fusion of digital pathology and transcriptomics.

I'm excited for the emerging integration of mIF and spatial multiomic data.

Building upon our previous newsletter, we are now exploring the constraints associated with saliva testing. This particular form of testing presents significant challenges within the realm of forensic biology, see the link below. #ForensicScience #BiologicalAnalysis https://lnkd.in/gGi_vaFg

Not sure where to start with your first spatial biology experiment? Let us help with our step-by-step guide to planning your first GeoMx DSP experiment! Learn how to choose morphology markers and decide on a region of interest selection strategy to maximize success for your first experiment. https://bit.ly/3RBSYBy With GeoMx DSP, you decide where to draw the line. #spatialbiology #spatialtranscriptomics #spatialproteomics

🔬 Delighted to spotlight our colleague and collaborator, Dr Elisabeth Kugler, AFHEA CSci MRSB., on this #FluorescenceFriday. 👁️ Dr. Kugler's image offers a detailed insight into zebrafish development, showcasing a digital section through the eye of a 2.5-day old specimen. Noteworthy is the visualisation of support cells' movement towards blood vessels, critical for nutrient supply and waste removal. 🔍 Acquired with a Zeiss LSM 900 AiryScan microscope, utilising a 40x water immersion LD C-Apochromat objective, the image demonstrates the precision and capabilities of modern microscopy techniques. 🌟 Commending Dr. Kugler's work in developmental biology, this image adds valuable insights to our understanding of cellular dynamics in early zebrafish development. #Science #Research #Microscopy #Zebrafish #DevelopmentalBiology #FluorescenceMicroscopy #Zeiss #LSM900 #AiryScan #STEM #Glia #mullerGlia #evodevo

Have you heard about the Diff-Quik? MGG Quick Stain? Whatever your answer is, you'll definitely enjoy what you're going to read right now! ⬇️⬇️ MGG: May Grunwald-Giemsa. It is a quick method for differential staining of formed blood elements. It can also be used to stain other types of air-dried smears (sediment smears, needle aspirates). The resulting staining can be compared to traditional May Grunwald-Giemsa method. Solutions in this kit contain the same dye as traditional May Grunwald and Giemsa solutions. Thanks to their high degree of dissociation, active molecules (eosin and thiazine dyes) can be absorbed by cellular structures very quickly. ⚠️WARNING⚠️ - It is important to immerse and extract specimen as requested in the method. A continuous permanence in the solution does not guarantee good staining results. - If the final staining shows unbalance between eosinophil and basophil components it is necessary to verify pH of washing water. If this value is very different from neutrality - pH 7 - we advise to use a buffer (ex. phosphate buffer pH 7 Bio-Optica) or distilled water. 🔬METHOD🔬 1) Dry the smear in the air. 2) Immerse the slide 5 times for 1 second each in solution A. After every immersion wait a moment to drain excess. 3) Immerse the slide 5 times for 1 second in solution B. After every immersion wait a moment to drain excess. 4) Immerse the slide 3-5 times for 1 second in solution C. After every immersion wait a moment to drain excess. 5) Wash in tap water. 6) Dry the slide in the air (do not use heat sources such as oven, etc.…). For more info: https://lnkd.in/dT8SN_hK. #mgg #quickstain #diffquick #histology #histopathology #clinicaldiagnostics #laboratory #bloodsmear #cytology #bio_optica #innovativemeditech #imt #gcc #uae #ksa #jordan