WOUND HEALING EVALUATION PARAMETERS : (i) Wound contraction and epithelization time The percentage wound contraction was determined using the following formula : Percentage wound contraction = Healed area x 100 Total area Wound contraction was measured plannimetically using a transparent paper in each four days interval. It was observed the after simple ointment base treatment, % wound contraction reached to maximum in 21days. Mean of epithelization time of polyherbal was found to be leaser (16day) compared to control groups (21 days). TABLE.7.1. Effect of Topical Application leaves of Azadirchta indica , Cassia fistula, Eucalyptus globulus & Bulbs of Allium sativum extract Polyherbal Formulation on Excision …show more content…
20µl of blood was diluted in 0.4 ml of the diluting fluid in a test tube. The cover slip was put on the counting chamber and then a small quantity of the diluted blood was put between the cover slip and ruled the platform of the counting chamber. The chamber was not be overflow and there was not be any air bubble in the chamber. The solution was allowed to settle for a couple of minutes and then the counting was done under the high power of a microscope. The WBC count is made in large (1 mm) corner squares of neubauer chamber. The numbers of cells in the 4 corner groups of 16 squares are counted. If the dilution has been 1 to 20 then the total number of cells in millions per mm3 of blood. Calculation: The 1 square has an area of 1 mm2 and is 0.1mm deep, being thus 0.1mm3/0.1µl in volume. Since 4 such squares are counted, a volume of 0.4 mm3/0.4µl has been covered. In order to give the value per mm3, the number of cells counted must be multiplied by 2.5. However, since the dilution is 1 to 20, the multiplication factor is 2.5 x 20. Cells/mm3= No. of cell counted in four square x 2.5 x
Prelab week 1 Calculations Preparation of 1.5μmol/L mixed low-level standard dilution 150μmol/L × V1=1.5μmol/L × 10ml V1=(1.5μmol/L×10ml)/(150μmol/L)=0.1ml Conversion of milliliters to microliters (0.1ml×1000)μL= 100μL Preparation of 3μmol/L mixed low-level standard dilution 150μmol/L × V1=3μmol/L × 10ml V1=(3μmol/L×10ml)/(150μmol/L)=0.2ml Conversion of milliliters to microliters (0.2ml×1000)μL= 200μL Preparation of 3μmol/L mixed low-level standard dilution 150μmol/L × V1=7.5μmol/L × 10ml V1=(7.5μmol/L×10ml)/(150μmol/L)=0.5ml Conversion of milliliters to microliters (0.5ml×1000)μL= 500μL Preparation of the blank samples The volumetric flask will be filled to the mark with 150μmole/L of stock solution to act as blank (reference). Additional two blanks will
The serial 2-fold dilution were done with a volumetric pipette, its pump, and 10 mL volumetric flasks. Eight different solutions were produced, half of which came from Red 40 and the other half, from Blue 1. These different concentrated solutions were placed in a 10 mL volumetric flask, each labelled with either R for Red 40
Problem 3 solutions using different approaches in the literature Approach Reference Machine cells Number of intercellular
In the lab “All That Glitters” the objective that was focused on during the lab was calculating the density, volume and mass of various substances. The method that was used in finding the volume of the samples is called the displacement method. This is a process where the volume of the water in the graduated cylinder is calculated before and after the sample is placed. In this lab, the goal of the experiment was to identify and come to consensus about what the unknown substance might be. For this experiment, the required materials were ten pre and post pennies, unknown sample, graduated cylinder, weigh boat, water, paper towels and a weighing scale.
The colour of each test tube was recorded and if proteins were present that was recorded for each test tube. Finally, the pH was recorded for each sample using pH
FOV Dia.(mm) FOV Area (mm^2) 10 10 10 100 2mm 4mm^2 20 20 10 200 1mm 1mm^2 40 40 10 400 .5 mm
ST Report In the experiment, the problem was the contaminants that were affecting the quality of the water samples. To fix this issue, three scientists had to determine the contaminants that were present in the samples. One sample was from the school sink and the second sample was from an unknown source. The scientists conducted many tests to figure out what pollutants were present in the water.
Background Research: Isopods are group of small, cold-blooded, crustaceans also known as pillbugs and sowbugs (pillbugs are commonly known as “roly polies”). Pillbugs are almost exactly like sowbugs, but differ because they can curl up into balls and are thicker than sowbugs (PNNL). Isopods are related to a few water crustaceans including crabs, crayfish, and shrimp, so water is necessary for them to survive. For that reason, they live in damp or wet areas such as forests and meadows. Isopods have seven armour plates, called “pereonites,” that serve as protection from predators and have seven pairs of legs.
For circulatory strain gages, every vast line parallels 10 mm Hg (millimeters of mercury) and every little line remains for 2 mm Hg. Attendants must make an interpretation of solution requests into the correct measurements and number of pills to control. Basically, the quantity of pills required equivalents the measurement sought isolated
\section{Facility Static and Dynamic Control}\label{Calibr} The facility calibration is the transfer function between the oscillating gauge pressure $P_C(t)$ in the chamber (described in ~\autoref{Sub31}) and the liquid flow rate $q(t)$ in the distributing channel, i.e. the test section. Due to practical difficulties in measuring $q(t)$ within the thin channel, and being the flow laminar, this transfer function was derived analytically and validated numerically as reported in ~\autoref{Sub32} and ~\autoref{Sub33}. \subsection{Pressure Chamber Response}\label{Sub31} Fig.\ref{fig:2a} shows three example of pressure signals $P_C(t)$, measured in the pneumatic chamber.
5 litres of 1x10^-2 Dodecylamin has been diluted to 1x10^-5M by adding accurate amount of water from the tap. To calculate required water amount mathematical equations given below : C1V1=C2V2 10^-2M x V1 =10^-5M x 1,000 mL V1 = 10^-5/10^ -2
The addition signs for each test on serum 2216 illiterates how concentrated the molecule is like purple for example was the most concentrated due to the amount of addition signs in the table. For Macromolecule test 1 and 2 the sample was diluted. Both the concentration and decreased by an equal set of intervals. The volume of distilled water is what was added and the results illustrate how deeply colored each concentration was. Each cup was diluted with the test pertaining to it with a syringe that explain the volume and the concentration is from heating or mixing the sample throughout the investigation.
FIll the third with another 90ml dh20 to reach 100ml. Move 10 ml of the third well to the fourth well. Fill the fourth well with 90ml dh20 to reach 100ml. Move 10 ml of the fourth well to the fifth well. FIll the fifth well with 90 ml of dh20 to reach 100ml.
The streaking technique used was a modified streaking for isolation with a heavy quadrant one. The result revealed that bacteria is alpha, with an incomplete breakdown of the medium with a susceptibility of 17mm from the bacitracin gamma hemolysis. That is why the organism represented by the bar graph was in low numbers because it was incomplete. The other test was DNase agar, it is an enzyme test used to identify if the organism has the enzyme DNA. The streaking technique is a single straight line down the middle of the plate.
Hypothesis: If we add pineapple and meat tenderizer to the gelatin, then it will not congeal. Materials needed: Gelatin, Fresh and canned pineapple, Meat tenderizer, Beakers, Cold and boiling water, a timer, 4-5 bowls, 4-5 test tubes and a rack, and a few spoons. STEPS Step 1.