BIOL308 Lecture Notes - Lecture 11: Antisense Rna, Ethidium Bromide, Aspergillus Nuclease S1

61 views2 pages

Document Summary

Proteins estimate the number/position of gene copies, restriction mapping. After electrophoresis, before nitrocellulose abundance of mrna at certain times/conditions, transcription/degradation rate. Naoh to break h bonds so ds ss (move on size), ethidium bromide in uv, capillary transfer with buffer, add light/heat to crosslink, radioactive probe, control/sense for non-specific binding. Electro-blot + incubate with specific 1* antibody & tagged 2* antibody then substrate to show colour (anti)sense ribo-probes based on dnap binding sites. 1: need a target with a chemical/radioactive (antisense rna) labelled probe for hybridization based on template and visualize with a detection system (x ray film, imaging, colour-o-metric) 2: make a probe with part of the cds from the same organism, gene cds from a difference organism, or sequence a gene from the same family as gene. 3: have the target bind the probe in a controlled manner based on percentage of sequence identity (complementarity) 4: controlled by stringency of hybridization and washes of probe (temperature, [salt])

Get access

Grade+20% off
$8 USD/m$10 USD/m
Billed $96 USD annually
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
40 Verified Answers
Class+
$8 USD/m
Billed $96 USD annually
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
30 Verified Answers

Related Documents

Related Questions