Answer:
The correct insulin pathway is described as under:
2. Binding of insulin to the alpha subunit of the insulin receptor
8. Activation of insulin receptor tyrosine kinase
3. Phosphorylation of IRS proteins
6. Phosphorylation of phosphinositide 3-kinase (PI-3K)
4. Conversion of PIP2 to PIP3
7. Activation of PIP3-dependent protein kinase B (PDK1)
5. Glut4 receptors transported to the cell membrane
Explanation:
The insulin signaling pathway is described as under:
RTK (receptor tyrosine kinases) which is a receptor for insulin is an extracellular receptor but in contrast to other cell surface receptors it is catalytic in nature. In the absence of insulin (ligand), it is monomeric but as soon as it gets activated (activation occurs upon ligand binding), it undergo dimerization. It leads to auto-phosphorylation in it's tyrosine residue which subsequently leads to phosphorylation of tyrosine residue of other receptors. Such hyper-phosphorylated receptor have high affinity with enzyme/molecule like IRS protein which have SH2 domain . IRS down stream activates phosphinositide 3-kinase (PI-3K). This enzyme converts component of animal cell membrane PIP2 into PIP3. PIP3 also remains membrane bound but it has the potential to phosphorylate another enzyme named as PIP3-dependent protein kinase B (PDK1). Further, PDK1 leads to the activation of Akt or PK-B. Akt is a serine-threonine kinase which ultimately leads to the recruitment of Glut4 receptors on cell membrane for uptake of more and more glucose into the cell.
Note: Apart from this Akt also phosphorylates another protein named as FOXO which ultimately causes cell growth, Akt can also phosphorylate BAD protein so as to restrict cell apoptosis or we can say it leads to cell survival, Akt also leads to translation in a cell with the help of mTOR raptor etc.
Answer:
DNA from a gene of interest can be inserted into a plasmid, then the modified plasmid can be inserted into a bacterial cell to replicate a gene of interest many times.
Explanation:
Plasmids are the extra-chromosomal circular DNA present in bacterial cells. Plasmids are able to replicate themselves independent of genetic DNA. Their ability to self replicate allows them to maintain themselves in the bacterial cells. This is why plasmids are used as cloning vectors in recombinant DNA technology.
A gene of interest is isolated from the donor cell and is inserted into the plasmid. The recombinant plasmid is introduced into bacterial cells where it replicates the ligated desired gene and allows the gene cloning. For example, the human insulin gene is ligated with plasmid and the recombinant plasmid is introduced in <em>E. coli</em> where it replicates the human insulin gene and allows the production of desired copies of the gene.
I believe the answer is an egg
Answer:
Atoms are electrically neutral as a result of having an equal amount of positive (due to the protons) and negative (due to the electrons) charges on it.
An ion generally is an electrically unbalanced atom (i.e an atom with a net charge on it)
A negative ion called an anion is produced when an atom gains an extra electron from a neighboring atom, giving it an extra negative charge. This can be produced by ionization with a radioactive radiation or simply by dissolution.
A positive ion is called a cation and it is produced when an atom loses electron to a neighboring atom. The loss of this electron causes the positive charges to outweigh the negative charges in the atom. Cations can be produced by radioactive radiation ionization of an atom or by simple dissolution.
The subatomic particle that is negative is the 'electron'.
