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Malarial Cell Culture - Science topic

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how H CQ+Azi acts against covid 19?
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Hi there!! I want to do quality check some Sanger sequence reads and realized that the reads contain some odd letters (N, K, Y, B etc) different from the normal 4 DNA base letters (ATGC). What can i do to edit away these strange nucleotides represented by the strange letters?
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These are not strange nucleotides, but they represent ambiguous peaks at those positions, and polymorphism. Each of these letter specific combinations of signals and are defined in the IUPAC list of ambiguous nucleotides. You need to check these positions in your sequence electrpherograms and confirm. If you have peaks of comparable intensity, you may retain these letters while submitting your sequences to the GenBank. GenBank accept sequences with IUPAC codes. Fllow the link while revising your sequences:
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i am a researcher in Nigeria and i need to induce Experimental cerebral malaria.
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We recently received some Plasmodium falciparum sporozoites cryovials which are frozen with HES (hydroxy ethyl starch),Trehalose and DOPC (Dioleoylphosphatidyl-Choline) based freezing solution. As we have no experience with these freezing solution, can I please ask if anyone can advice us what principle should we follow when we thaw these cells (also would be fantastic if anyone can provide us a thawing protocol for similar conditions)?
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I do not know your application but I have used the trehalose based freezing solutions with human epithelial cells.  We thawed the cells the same way with any cryo-media, Fast.  Threhalose is not considered toxic.  Similar to raffinose or other branched carbohydrates.
General procedure:
1. Vials were swirled by hand in a 38 C water bath. 
2.  As soon as the lat remnant of ice disappears, we very gently diluted the crryo-media 10 fold
3. cells allowed the cells to rest for 30mins-1 hour in aerobic conditions. 
The thaw is the highest stress point for cells in the cryopreservation procedure.  Respiration restarts and membranes have to be repaired.  Between the damaged membranes and the superoxide generation, not all cells will make it out of cryo.
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Dear Colleagues,
I am looking for the public domains with blood slide images infected with Malaria disease and their corresponding manual parasitemia (degree of Malaria infection) results. I will use these results to validate the accuracy of my model, which does automatic parasitemia detection. The model I am trying to propose does not require manual counting of the infected red-blood-cells using microscope, but its accuracy needs to be compared with the existing classical approach of manual counting.
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Hello Baraka,
The best way u can go about it is what Lamoussa had adviced. 
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I am looking to get experience in malarial cell culture and animal model study. Could anyone suggest any lab or center, where anti-malarial or any malarial study is going on, so I can approach for training ?
I already tried to contact NIMR (Chennai & Delhi) and also CDRI in Uttar Pradesh. No response form them.
Any suggestions guys?
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Regional Público Health Centre; before as Malaria Research Center. Contact Ildefonso Fernandez: ifernand1@hotmail.com