Answer:
H20
Explanation:
Because without water you will die faster then without food
<span>it probably break apart with cleavage, because the carbon atoms in graphite from sheets that could split apart easily in layers.</span>
Answer:
The cell interior would experience higher than normal Na+ concentrations and lower than normal K+ concentrations.
Explanation:
Na+/K+ ATPase exists in two forms: Its phosphorylated form has a high affinity for K+ and low affinity for Na+. ATP hydrolysis and phosphorylation of the Na+/K+ pump favor the release of Na+ outside the cell and binding of K+ ions from the outside of the cell. Dephosphorylation of the pump increases its affinity for Na+ and reduces that for K+ ions resulting in the release of K+ ions inside the cells and binding to the Na+ from the cells.
The presence of ATP analog would not allow the pump to obtain its phosphorylated form. Therefore, Na+ ions would not be released outside the cells. This would increase the Na+ concentration inside the cell above the normal. Similarly, the pump would not be able to pick the K+ from the outside of the cell resulting in reduced cellular K+ concentration below the normal range.
Science method. like the gemdas is math there’s a process for science which depends on chem or bio.
Answer:
gDNA = "genomic DNA" and cDNA = "complementary DNA." cDNA is classically associated with being reverse transcribed either from all extracted RNA from a tissue or cell (total RNA) including (in eukaryotes) pre-mRNA, ribosomal RNA, tRNA, snoRNA, miRNA and mRNA, etc.) while cDNA obtained only from reverse transcription of the mRNA (expressed eukaryotic cytosolic mRNA) fraction (e.g., by poly[dT]n and random priming) is complementary DNA (cDNA) made from what is called the "transcriptome." Eukaryotes have introns and exons in the gDNA, while prokaryotes do not. So eukaryotic cDNA reverse transcribed from mRNA lacks introns. Prokaryotic-derived cDNA is always complementary to prokaryotic RNA and gDNA (so is always necessary to have a good DNase treatment prior to gene expression analysis by e.g., qPCR for prokaryotic transcriptome work)...