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Abnova
Добавлен 21 сен 2009
A professional biotechnology education channel
Видео
Spiraltor™ 48 mRNA Oligo (dT) purification
Просмотров 973Год назад
An automated system performing mRNA Oligo (dT) purification is shown in this AbVideo. Spiraltor™ 48 - Spiral-Mix Magnetic Bead Handling is a patented spiral-mix, magnetic bead handling system for high throughput mRNA purification. Combining 48 channel open platform with oligo (dT) magnetic beads, Spiraltor™ 48 easily handles 48 different assays simultaneously by transferring beads from one well...
Demonstration of Abnova Precipitor™ 32
Просмотров 1,3 тыс.3 года назад
Abnova’s Precipitor™ 32 system is an automated magnetic bead platform for high throughput extraction, purification, and precipitation. Combining 96 deep well plate with conjugated magnetic beads, Precipitor™ 32 easily handles 32 different assays simultaneously by transferring beads from one well to the next for mixing, binding, washing, and elution reactions via the robotic action of parallel m...
亚诺法 x 艾美捷 - 生技界的成功合作典范
Просмотров 6443 года назад
这几年来中国大陆生技产业蓬勃发展,科研产品的需求量大幅成长;亚诺法很荣幸能与艾美捷长期合作,为大陆科研尽一份心力。
2019 Abnova Hot Summer Sale
Просмотров 1,4 тыс.5 лет назад
Hot Summer Sale www.abnova.com/activity/promo/2019SummerSale.asp Date: 2019/6/12 00:00 - 2019/6/13 23:59 EDT Discount: 30% Off Product on Sale: All product types except made to order and systems If you have any questions, feel free to contact us at marketing@abnova.com.tw
SpiralPipet™
Просмотров 1,3 тыс.5 лет назад
Abnova’s SpiralPipet™ is a patented spiral-mix, magnetic bead handling system for high throughput precipitation, purification, and extraction. For more information, please go to bit.ly/2YvXpAx Interested in this product? Feel free to contact us: sales@abnova.com
CytoQuest™ CR Automated Leucosep Preparation
Просмотров 6215 лет назад
( www.abnova.com ) - An automated system performing PBMC extraction is shown in this AbVideo. After Leucosep preparation, cells can either be banked or followed by downstream CTC enumeration using CytoQuest™ CR. Abnova’s CytoQuestTM CR is a non-invasive system for capture, enumeration, isolation and retrieval of circulating rare cells (CRCs), including circulating tumor cells (CTCs), circulatin...
mutaFISH™ - How it works
Просмотров 4,8 тыс.5 лет назад
Abnova has integrated padlock probe and rolling circle amplification (RCA) for in situ, single cell, single molecule, DNA and RNA mutation detection at single nucleotide resolution.
CytoQuest™ CR Bubbles & Microfluidics - Dos & Don'ts
Просмотров 7555 лет назад
The AbVideo focuses on how to prevent bubble formation inside sample, microfluidic tubing or plugs when performing Cell Capture using CytoQuest™ CR.
mutaFISH™ Circulating Tumor Cell
Просмотров 1,4 тыс.5 лет назад
A thorough description on how to perform mutaFISH™ staining in situ in circulating tumor cells captured in CytoChipNano. Abnova’s mutaFISH™ probe are for in situ, single cell, single molecule, DNA and RNA mutation detection at single nucleotide resolution. In this video, mutaFISH™ EGFR L858R L858wt Ex19wt RNA Probes is used for demonstration. Please visit Abnova website for more information of ...
mutaFISH™ Frozen Tissue
Просмотров 7785 лет назад
A thorough description on how to perform mutaFISH™ staining in situ in frozen tissue. Abnova’s mutaFISH™ probes are for in situ, single cell, single molecule, DNA and RNA mutation detection at single nucleotide resolution. In this video, mutaFISH™ EGFR L858R L858wt Ex19wt RNA Probes is used for demonstration. Please visit Abnova website for more information of mutaFISH™ products.
CytoQuest™ CR Capture Antibody Immobilization
Просмотров 1,3 тыс.5 лет назад
( www.abnova.com ) - This AbVideo demonstrates step by step protocol of antibody immobilization on CytoChipNano before cell capture. Abnova’s CytoQuest™ CR is a non-invasive system for capture, enumeration, isolation and retrieval of circulating rare cells (CRCs), including circulating tumor cells (CTCs), circulating stem cells (CSCs), and circulating fetal cells (CFCs). Please visit Abnova web...
CytoQuest™ CR Cell Capture
Просмотров 1,3 тыс.5 лет назад
( www.abnova.com ) - CytoQuest™ CR Cell Capture AbVideo focuses on system operation including processes on parameters and settings, system priming, buffer filling, sample loading and capturing. Abnova’s CytoQuest™ CR is a non-invasive system for capture, enumeration, isolation and retrieval of circulating rare cells (CRCs), including circulating tumor cells (CTCs), circulating stem cells (CSCs)...
AbLearning™ - Episode 5: T Cell Immunometabolism
Просмотров 5 тыс.6 лет назад
AbLearning™ - Episode 5: T Cell Immunometabolism
AbLearning™ - Episode 4: Chimeric Antigen Receptor T Cell Therapy: Efficacy & Safety
Просмотров 17 тыс.6 лет назад
AbLearning™ - Episode 4: Chimeric Antigen Receptor T Cell Therapy: Efficacy & Safety
AbLearning™ - Episode 3: Chimeric Antigen Receptor T Cell Therapy
Просмотров 2,9 тыс.6 лет назад
AbLearning™ - Episode 3: Chimeric Antigen Receptor T Cell Therapy
AbLearning™ - Episode 2: Circulating Tumor Cell Isolation
Просмотров 1,8 тыс.6 лет назад
AbLearning™ - Episode 2: Circulating Tumor Cell Isolation
AbLearning™ - Episode 1: Circulating Tumor Cells
Просмотров 10 тыс.6 лет назад
AbLearning™ - Episode 1: Circulating Tumor Cells
CytoQuest™ CR CTC Post Leucosep Freezing and Banking
Просмотров 2959 лет назад
CytoQuest™ CR CTC Post Leucosep Freezing and Banking
CytoQuest™ CR Plugs Assembly & CytoChipNano Placement - Dos & Don’ts
Просмотров 1879 лет назад
CytoQuest™ CR Plugs Assembly & CytoChipNano Placement - Dos & Don’ts
CytoQuest™ CR SCx™ Spiral Chamber Assembly - Dos & Don’ts
Просмотров 3369 лет назад
CytoQuest™ CR SCx™ Spiral Chamber Assembly - Dos & Don’ts
latest video : H&E Staining | Purpose of staining in histopathology | Human Touch in H&E Staining : ruclips.net/video/WBUriohMkSM/видео.html
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🙏🙏🏻😊
every nice even after 14 years
Do I need to resuspend after adding MTT solution?
Would be better to desribe the function of each buffer and stripping reagent rather than the music in the background.
systematically demonstration of video. love this short way for whole day prep🥰
How I kmow DMSO will be under 1% after adding cells? How to do the calculation?
In my lab, we thaw the cryovial, then centrifuge it and remove the media using pipette. After that we add fresh medium in the vial resuspend with the cell pillets.Then transfer it to the 7 ml of media.Directly adding cells with dmso in our lab make our cells dead.Our cel line is HELA adn MDA-231.
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can you please tell me the molarity of this two solutions
can i use this precedure for total RNA extraction from brain tissue
why we used DMSO?
After centrifugation with isopropanol, I get 2 layers? Is it ok
Cheer~~~determine the content or quality of (a metal or ore).
The video is 13 years old, protocol has updated since then. Those days this was the method. Today the protocol is modified so follow the latest procedures. Overall, the basic principle will always remain same. ✌
song name?
6:27 What is that purple solution?
Sir Why use parafilms only ?
خب بابا میدونیم میدونید بیدارم زنگ زدن نمیخواهد که
Your thumbs are contaminating the sample.
to fix the antigen, can I replace the paraformaldehyde with formaldehyde?
what is the name of this lab please? i want to apply for PhD studies they looks so amazing
I am interested in finding out if the smallest surface ( that with volume signs) of the flask is treated for cell culture.
Thank you for your informative video. I was wondering if 1mM PMSF is added to 10 ml of RIPA lysis buffer. It would be great if you could clarify the exact amount of RIPA lysis buffer.
Thank you 🙏
Song is a banger a 2x speed
Great lesson😊
Reading the protocol - the volume of Trizol needs to be titrated according to the volume of cells to be obtained, and whether the cells have been grown in monolayer or suspension. Trizol is quite powerful so can degrade the cells and RNA altogether. Don't use 1 mL Trizol uniformly - only the volume you need. The volume of Trizol affects the volume of Chloroform, Isopropanol and Ethanol to be added later in the reaction.
this is stupid and convoluted find a way to do this in one pot. dont waste my time
Taking my baby steps into research, your videos have helped a lot!
Hi, thanks for the video. Please, I have a question: I will like to ask a question about cell treatment experiment with a test drug for 72 h. In such an experiment, do I have to add my drug once and incubate for 72h then check the cell viability or I have to remove the drug solution and replace with the same drug and concentration after each 24h to avoid wrong readings due to degraded drug in wells or evaporation? Please any other person reading the comments can also reply me if you have the correct answer to my question. Thank you
Could you please explain the steps of rehydration ( what you used and how much time in each bath) thank you .
can you tell me about cell line name? i really want to know that..
Very nice
Таке собі
Good music
Soo helpful thankss
What happens if you incubate at room temperature the primary antibody?
nice analyses
I appreciate the video warning against late behavioral/social interventions in the "Wait and See" method. By then, it is a game of catch up of addressing side effects while trying to get to the root cause. Giving extra support may provide different mileage, but withholding has much more drastic implications.
Please tell me if the sample could be a plasma or a serum from patients aimed at the determination of their protein or antibodies concentrations ?
Wats the pink solution that is removed at the beginning of the video?
The culture media most probably
Fantastic
Hello, I have two questions 1. After collecting my sample and adding Trizol, can i store it in -20C for a month? 2. Why we must change centrifugation 12000g to 7500g in etoh wash step? Can i perform this step with 12000g?
Why the upper phase is red, phenol-chloroform phase and the lower phase is aqueous ?
the website that you have provided is not working / not found for optimization of IEF program
y this is not working with DNA fasta file
Does the T25 flask has the cap without holes when it arrived ? If yes could be used for cell culture especially if we loose the cap as you probably did before injcubation?
can i do my mtt not inside the bisafety cabinet?