True because carbohydrates are in the cell membrane.
The correct order of steps in an experiment would be:
- Identify the variables.
- Write out your hypothesis in an if/then format.
- Gather your materials.
- Analyze the data.
- Write your conclusion.
<h3>What is an experiment?
</h3>
An experiment is a term to refer to the process by which a hypothesis is supported/disproved. The experiments serve to explain the cause-and-effect relationship according to the results obtained.
Experimentation has some important steps that we must follow to demonstrate our ideas regarding a scientific manifestation, these steps are:
- Identify the variables: We must identify the factors that we can manipulate so that the result changes.
- Write our hypothesis: Establish a hypothetical result that we are going to demonstrate.
- Gather the materials: We must have all the materials and variables to be able to carry out our experiments.
- Analyze the data: When we do an experiment we must record everything we see and then analyze it to examine each step and the procedures performed.
- Write the conclusion: After analyzing the data obtained, we can write a conclusion about the experiment carried out and the result obtained.
Learn more about experiments in: brainly.com/question/9199868
The genetic fault that usually causes colour vision deficiency is passed on in what's known as an X-linked inheritance pattern.
This means:
1) it mainly affects boys, but can affect girls in some cases
2) girls are usually carriers of the genetic fault – this means they can pass it on to their children, but do not have a colour vision deficiency themselves
3) it's usually passed on by a mother to her son – the mother will often be unaffected as she'll normally just be a carrier of the genetic fault
4) fathers with a colour vision deficiency will not have children with the problem unless their partner is a carrier of the genetic fault
5) it can often skip a generation – for example, it may affect a grandfather and their grandson
6) girls are only affected if their father has a colour vision deficiency and their mother is a carrier of the genetic fault