Negate stain in ODOC

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Aug 6th, 2022
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How to negate stain in ODOC

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appreciate this job today oil stain removal you see the patch here is quite bad and Iamp;#39;m just going to treat it with some resin cloth or stain remover now itamp;#39;s really important when you use this that the stain is dry so you canamp;#39;t use it once youamp;#39;ve started pressure washing and the blocks have become wet but just apply the oil stain across the stain and Iamp;#39;m going to give it a bit of a scrub but agitate it and then pressure wash it away once itamp;#39;s sat there for a few minutes as well and now Iamp;#39;m going to go away do another job nearby come back once itamp;#39;s dried out again and check it it might need a second application but you canamp;#39;t do the second application until itamp;#39;s dried out and reapply it once once itamp;#39;s dried out again so thatamp;#39;s what weamp;#39;re going to do show you how we get on okay so now Iamp;#39;m going to pressure wash the area using the turbo nozzle here itamp;#39;s t

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Heat damages certain cellular features including bacterial glycocalyx (capsules and slime layers), therefore we do not heat fix when negative staining.
Negative staining employs the use of an acidic stain and, due to repulsion between the negative charges of the stain and the bacterial surface, the dye will not penetrate the cell. In negative staining, the results yield a clear cell with a dark background.
URANYL ACETATE A 1% to 3% solution of uranyl acetate dissolved in distilled water (pH 4.2 to 4.5) can be used to negatively stain many types of samples. The stain should be filtered through a 0.22 m filter that has been pre-rinsed with large volumes of double distilled water.
1. Place 3- 50 l drops of sterile water and 2- 50 l drops of 2% UA on parafilm 2. Apply 4 l of sample onto glow discharged grid for 40 sec 3. Gently blot the sample (Whatman #1 filter paper).
Negative Staining Procedure If you are working from a plate culture, add a drop of sterile water to the slide and dilute your organism in the drop without spreading the drop. Put one or two drops of nigrosin on another slide. Use your sterilized loop to pick up a loop-full of nigrosin.
Negative staining protocols. The conventional negative staining protocol involves the adsorption of the specimen to a glow-discharged carbon-coated EM grid, which is washed with two drops of deionized water and subsequently stained with two drops of heavy metal solution.
Negative Staining Take two slides. Place a drop of acidic dye, nigrosin, at one end of your slide. Place your specimen into the dye and swirl it in the stain. Using the other slide, hold it at a 45 angle and feather the mixture across the slide by pushing the dye. Air dry but do NOT heat fix. Observe your negative slide.

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