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dalvyx [7]
3 years ago
12

Glucose travels in the plasma or liquid part of

Biology
1 answer:
djverab [1.8K]3 years ago
3 0

Answer:

Explanation:

Glucose is a sugar, highly soluble in water because it has lots of polar hydroxyl groups (-OH) which can form hydrogen-bonds with water molecules. These types of bonds are intermolecular forces which are present in other macromolecules like the DNA or proteins.

Cholesterol and triglycerids are lipids. These have long chains of hydrocarbons, which are non polar and therefore insoluble in water.

Blood is made of a solid and a liquid part. <u>The solid part contains cells</u>. <u>The liquid part (plasma), is made of water, salts, and proteins</u>. Glucose and cholesterol/triglycerids travel in the liquid part of the blood, in an aqueous environment. Because the lipids are not soluble, they need to travel with a carrier protein that keeps them protected from the surrounding water.

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damaskus [11]

When ice forms, one water molecule's hydrogen atoms form weak hydrogen bonds with the tops of the oxygen atoms of two other water molecules. Lining up the water molecules in this pattern takes up more space than randomly arranging them.

<h3>What is polarity?</h3>

A physical property of compounds that connects other physical properties like melting and boiling points, solubility, and intermolecular interactions between molecules is referred to as polarity.

When ice forms, one water molecule's hydrogen atoms form weak hydrogen bonds with the tops of the oxygen atoms of two other water molecules.

Lining up the water molecules in this pattern takes up more space than randomly arranging them.

When water freezes, the water molecules slow down enough that their attractions arrange them into fixed positions. Water molecules freeze in a hexagonal pattern, with molecules further apart than when the water was liquid.

Thus, because of this frozen water take on the pattern it does.

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Which of the following describes the structure formed when a probe
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3 years ago
huntington disease is a dominant disease caused by expansion of the trinucleotide repeat region of the htt gene that results in
Travka [436]

By haphazardly introducing a transgene harboring a disease-causing mutant variant of the HTT gene into the genome of a mouse or primate, it is possible to produce an animal model with the majority of the symptoms of this condition. Here option B is the correct answer.

Huntington's disease is an uncommon, genetic condition that results in the gradual degeneration of brain nerve cells. Huntington's illness, which frequently results in mobility, cognitive, and psychological problems, has a substantial impact on a person's functional capacities.

A DNA region known as a CAG trinucleotide repeat is involved in the HTT mutation that causes Huntington's disease. Three DNA-building building pieces that are repeated several times in a row make up this region.

Complete question:

Huntington's disease is a dominant disease caused by the expansion of the trinucleotide repeat region of the Htt gene that results in the production of a Huntingtin protein with an expanded number of glutamines. An animal model with most features of this syndrome could be created by

A - knocking in a wild-type copy of the Htt gene to a mouse or primate genome.

B - randomly inserting a transgene containing a wild-type allele of the Htt gene to a mouse or primate genome.

C - randomly inserting a transgene containing a disease-causing mutant allele of the Htt gene into a mouse or primate genome

D - knocking out one copy of the wild-type Htt gene from a mouse or primate genome.

E - knocking out both copies of the wild-type Htt gene from a mouse or primate genome.

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3 0
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