What’s the question!!!!!!!!!!!!!!
Answer:
forming
Explanation:
Team development is a process wherein different individuals come together and learn to work efficiently to carry out a specific task.
There are certain stages that a team goes through during the development phase and these are:
1. Forming
2. Storming
3. Norming
4. Performing
5. Adjourning
The stage of team development where the different members get to know each other and orient themselves concerning each other's space is known as forming. This is a stage where they get acquainted with each other and explore and learn the ideas fo different team members.
Since in the given situation the scientists and dentists are holding a team meeting to get acquainted with each other and formally introducing themselves, the team is currently in the development stage of forming.
Answer:
Gene knockout is a technique used to determine the function of a gene that has already been sequenced, which is achieved by analyzing the phenotype of the individual carrying the knockout mutation(s). Moreover, gene sequencing is a technique used to determine the sequence of a given gene, which allows to determine how gene variants (polymorphisms) may be associated with the phenotypes of the target trait.
Explanation:
In genetics, gene knockout is a technique used to trigger mutations in a (already) sequenced gene in order to inactive its function and observe the resulting phenotype for a particular trait. This approach that starts with the inactivation of a given gene and ends with the phenotype is known as reverse-genetics. On the other hand, gene sequencing can be defined as the methodologies/techniques/tools used to determine the nucleotide base pair sequence of a particular gene. The gene knockout technique involves knowing a priori the gene sequence in order to obtain a gene knockout (gene KO). The combination of the information obtained from these techniques can be used to determine how variation (genetic variation) affects the expression of a phenotypic trait.
Answer:
<h2>
Haploid=13</h2><h2>
triploid=39 </h2><h2>
tetraploid=52</h2><h2>
trisomic=14 </h2><h2>
monosomic=12</h2>
Explanation:
Given;
A species with a diploid number of 26, so 26= 2n ( a diploid cell),
so in haploid condition, chromosome number becomes half (13 in this case). triplod is when 2n + n, and 2n +2n ( tetploid). Trisomy and monosomy is the addition or deletion of a sinlge chromosome of a sinlge set .
Haploid=13, one chromosome from each pair of chromosome set,
triploid=39 (13× 3); diploid+ n( 3n)
tetraploid=52 (13× 4) 4n
trisomic=14 (13+1) ; n+1
monosomic=12 (13-1); n-1
