Common questions

How to use a story sequence graphic organizer?

How to use a story sequence graphic organizer?

This is a story sequence graphic organizer. Students can use this graphic organizer to tell a story and include details about the first, next, and last parts of the story. There is space for a picture for each part as well. Thank you for your interest in my item! This is a story sequence graphic organizer.

What can you do with first then next graphic organizer?

This is a story sequence graphic organizer. Students can use this graphic organizer to tell a story and include details about the first, next, then, and last parts of the story. There is space for a picture for each part as well. Thank you for your interest in my item!

Which is the best description of the creert2 model?

Model Description. Successful ubiquitous induction of Cre activity after tamoxifen administration in all tissues analyzed. Efficiency of deletion varies between different organs and different loxP flanked (floxed) target genes but usually exceeds 70%, except in the brain were deletion efficiency is lower.

Are there any discrepancies in the Addgene sequence?

Discrepancies between sequencing results obtained by Addgene and the original sequence provided by the depositor may be present. Addgene has sequenced portions of this plasmid for verification. The results are shown below. Leading primers are indicated on the first line of each sequence.

Is the cloning site in pgr106 the same as PGR 107?

Both pgR106 and pgR107 are binary vectors based on pGreen0000, they are basically the same vector except that the cloning site in pgR106 contains ClaI-AscI-NotI-SalI, while in pgR107 contains CalI-SmalI-SalI.

Which is a better selection marker for pgr106?

Therefore pgR106 is more suitable for cDNA library construction, while pgR107 is more suitable for PCR product cloning considering the SmaI site in its cloning site. The selection marker for pgR106 and pgR107 is kanamycin (50ug/ml).