Would gene chips containing bacterial DNA segments be useful for monitoring gene expression in a mammalian cell?

Alternative splicing allows an organism to express different versions of a gene in different cells carry more genes produce fewer proteins express more than one gene from the same promoter

Compare the auto induction media (AIM) with regular induced protein expression. Which is better when conducting experiments?

How is the T7 bacteriophage regulated expression exploited in molecular biology?

After sequencing a new genome for the first time, functional protein-coding genes are initially identified by:     BLAST searches that look for viral integration in the host genome     Bioinformatic searches that reveal consensus sequences in expressed genes     Aligning expressed exons sequenced from cDNA using transcriptomics     B and C     A and B Many regions of non-coding eukaryotic DNA previously thought to be "junk" are now known to contain sequence elements important to regulating gene expression. What approach can be used to identify important non-coding regulatory regions when annotating a newly sequenced genome?     comparing cDNA to genomic DNA to validate that the gene is expressed     identifying restriction enzyme recognition sequences in the genome     phylogenetic footprinting to identify conserved non-coding sequences     searching for start/stop codons and splice recognition sites that predict where a gene might be located…

What gene expression question could you answer using data from the ENCODE website?

you design an ideal promoter for a gene to be highly expressed in E. coli cells? Describe strategies and explain