The answer to this question is the Pyers
patches. The Pyers patches are lymphatic tissues found through
the small intestines that have an important role in the immune system. Pyers
patches are also known as the aggregated lymphoid nodules that monitors and
prevents growth of bacteria in the intestine that is harmful in the intestines.
Answer:
The correct answer is - a. If these two mite chromosomes have different genes at different loci.
Explanation:
If it is 2n= 2, it means that it is diploid and has two sets of chromosomes in which one set comes from mother and the other from father which means parent's genes contribute to diploid equally. Both sets of chromosomes form homologous chromosome pair. Each homolog of the pair has the same gene at the same loci in diploid and if it has not the same homologous gene at the same loci these are haploid.
Answer:
a. ciliary body: focus the pupil
Explanation:
The choroid thickens behind the iris and forms the circular ciliary body. Ciliary muscles are present in the ciliary body. The lens is attached to the ciliary body by ligaments. The function of the ciliary body is to holds lens in place and to serve in accommodation.
When focusing on a distant object, the relaxed ciliary muscles make the lens is flat and the suspensory ligament is taut. When focusing on a near object, the contraction of the ciliary muscles of the ciliary body allows the lens to accommodate. The lens becomes rounded causing the suspensory ligament to relax. Thereby, the ciliary body regulates the shape of the lens for near and far vision.
Based on the information, you can determine that color-blindness is X LINK RECESSIVE.
C) X-linked recessive.
<u>Explanation:</u>
Color blindness is the common hereditary condition that is hereditary passed from their parents. The gene for the color blindness found in the chromosomes. So for the male to be color blind. X linked color blindness is the recessive traits.
Female heterozygous of the trait have a normal vision. The X link recessive is the mode of the inheritance in which the mutation of the gene on the chromosomes causes the depletion in the phenotype because the male has one Y and one x chromosomes.
Answer:
It is expected to observe the immunoprecipitation of the GST-tagged KinY complex, thereby indicating the role of RegX in the mechanism of cytoskeletal reorganization.
Expanation:
Western blot is a technique widely used in molecular biology laboratories in order to identify proteins and also to quantify their expression levels. This technique is useful to detect proteins with high specificity, in this case the technique has been used for the detection of an immunoprecipitated (i.e., GST-tagged KinY complex) in order to confirm the role of the upstream protein RegX in cytoskeletal organization.
