Answer:
Igneous rocks are formed from cooled magma, magma is formed from melted metamorphic rock, metamorphic rock is formed from either heated igneous rock or heated and pressurized sedimentary rock, sedimentary rock is formed from sediments throught compaction and cemenetaion and sediments are formed from weathered and eroded igneous or metarmorphic rocks
Explanation:
For more info look up rock cycles and hit images for a simple format
Answer:
The large intestines, liver, body, and lungs are included
Explanation:
Excretion is the mechanism by which waste and excess water are eliminated from the skin. It's one of the key ways that homeostasis is maintained by the body. Although kidneys are always the key excretion organs, a number of organs are also excreting waste. The large intestines, liver, body, and lungs are included. The excretory system is made up of all of these organs of excretion, along with kidneys.
Answer:
Is an animal that can be dependent or able to get internal generation from heat. So basically a warm blooded animal.
The answer would be C. A haploid cell.
Gametes are haploid cells made by meiosis. Male and female gametes fuse together during fertilization and form the diploid zygote.
The structure of a typical antibody molecule
Antibodies are the secreted form of the B-cell receptor. An antibody is identical to the B-cell receptor of the cell that secretes it except for a small portion of the C-terminus of the heavy-chain constant region. In the case of the B-cell receptor the C-terminus is a hydrophobic membrane-anchoring sequence, and in the case of antibody it is a hydrophilic sequence that allows secretion. Since they are soluble, and secreted in large quantities, antibodies are easily obtainable and easily studied. For this reason, most of what we know about the B-cell receptor comes from the study of antibodies.
Antibody molecules are roughly Y-shaped molecules consisting of three equal-sized portions, loosely connected by a flexible tether. Three schematic representations of antibody structure, which has been determined by X-ray crystallography, are shown in Fig. 3.1. The aim of this part of the chapter is to explain how this structure is formed and how it allows antibody molecules to carry out their dual tasks—binding on the one hand to a wide variety of antigens, and on the other hand to a limited number of effector molecules and cells. As we will see, each of these tasks is carried out by separable parts of the molecule. The two arms of the Y end in regions that vary between different antibody molecules, the V regions. These are involved in antigen binding, whereas the stem of the Y, or the C region, is far less variable and is the part that interacts with effector cells and molecules.
