Answer:
A) Cytoplasm
B) Chloroplast
C) Plasma membrane
D) Cell membrane
E) Smooth endoplasmic reticulum & Rough endoplasmic reticulum
F) Cell wall
Explanation:
Look at the picture below
A Negative stain such as India ink or Congo red-Look for the presence of a capsule.
This stain method is usually used to stain the area around the microorganism.
B The Gram stain-Divide bacteria into two groups based on cell wall structure (thick vs. thin).
This is type of differential staining used to distinguish organisms based on their staining properties. Gram + and Gram- bacteria stain different because of different cell wall structure.
C The Ziehl-Neelsen Acid-fast stain- Identify bacteria with waxy cell walls such as: Mycobacterium tuberculosis (the cause of TB).
This is also differential staining method which uses heat and phenol to derive dye into the cells with lipid-rich walls.
D Simple stain with a basic dye-Stain microbes a bright color to make it easier to see them in bright field microscopy.
One dye is used in simple staining in order to determinate the size, shape and arrangement of the cells.
E The Schaeffer-Fulton Endospore stain-Identify Bacillus or Clostridium species, such as the causative agents of anthrax, botulism, tetanus and gangrene.
This is a special type of staining only used for the bacteria that can form endospores. Bacteria are first treated with heat and then with malachite green, which is very strong stain that can penetrate endospores.
For the answer to the question above,
<span>DNA is made up of two nucleotide strands. The nucleotides are connected together by covalent bonds within each strand. The sugar of one nucleotide forms a covalent bond with the phosphate group of another. The two strands themselves are connected by hydrogen bonds. The hydrogen bonds are found between the bases of the two strands of nucleotides. Adenine forms hydrogen bonds with thymine whereas guanine forms hydrogen bonds with cytosine. This is called complementary base pairing</span>
I think theres a few methods to do it, but this is probably the most efficient.
Physician has prescribed 2.5% of 500ml
Actual amount of Aminosyn in this prescription is
500*0.025= 12.5ml of Aminosin
Therefore you need to ensure when you pour your solution of the 8.5% Aminosyn, it has 12.5 ml of Aminosyn.
To work out how much 8.5% Aminosyn you should pour, you must think of the 12.5ml as 8.5%
Therefore 1% = 12.5/8.5= 1.470588
Therefore the amount of 8.5% solution you need to pour is 100* 1.470588= 147.1ml
Then make up the rest(352.9ml) by adding distilled water. You now have 500ml of 2.5% aminosyn.
