logging in or signing up BLOTTING TECHNIQUES aSGuest135653 Download Post to : URL : Related Presentations : Let's Connect Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Copy embed code: Embed: Flash iPad Dynamic Copy Does not support media & animations Automatically changes to Flash or non-Flash embed WordPress Embed Customize Embed URL: Copy Thumbnail: Copy The presentation is successfully added In Your Favorites. Views: 1997 Category: Entertainment License: All Rights Reserved Like it (1) Dislike it (0) Added: May 22, 2012 This Presentation is Public Favorites: 2 Presentation Description No description available. Comments Posting comment... Premium member Presentation Transcript BLOTTING TECHNIQUES: BLOTTING TECHNIQUES Faisal Qaseem 08- arid-876 M.Phil Botony 2 nd semesterWhat is blotting? : What is blotting? Technique for transferring DNA RNA Proteins onto a carrier so they can be separated, and often follows the use of a gel electrophoresis.TYPES OF BLOTTING TECHNIQUES: TYPES OF BLOTTING TECHNIQUES BLOTTING TECHNIQUES Southern Blot It is used to detect the DNA. Northern blot It is used to detect the RNA. Western blot It is used to detect proteins.Blotting sheet : Blotting sheet Whatman 3mm paper….. world’s most widely used blotting paper. REASON???? high quality purity consistency (0.34 mm) is used extensively in electrophoresis for lifting of sequencing gels.Creating the Sandwich : Creating the Sandwich The sandwich consists of : filter paper Nitrocellulose membrane gel matrix another piece of filter paperSOUTHERN BLOTTING : SOUTHERN BLOTTING History: Named after Sir Edwin Southern Developed in 1975SOUTHERN BLOTTING : SOUTHERN BLOTTING “Used to detect the DNA” This method Involves: Separation Transfer H ybridization . This DNA can be: Single gene Part of a larger piece of DNA……..viral genome “The key to this method is Hybridization”Hybridization: Hybridization “Process of forming a dsDNA molecule between a ssDNA probe and a ss-target patient DNA”PRINCIPLE : PRINCIPLE The mixture of molecules is separated . Immobilized on a matrix . Probe addition to the matrix to bind to the molecules . Unbound probes are removed. “The place where the probe is connected corresponds to the location of the immobilized target molecule .”Steps in southern blotting : Steps in southern blotting The DNA is digested Fragments Gel electrophoresis Transfer to membrane Probing AutoradiogramAPPLICATIONS : APPLICATIONS Southern blotting is used in: Gene discovery Mapping Evolution Development studies Diagnostics ForensicsNorthern Blotting: Northern Blotting History: Northern blotting was developed by James Alwine and George Stark at Stanford University. Northern blotting is a technique for detection of specific RNA sequencesSteps involved in N.B : Steps involved in N.B RNA isolation Loading of sample on Agarose gel Blotting on nitrocellulose membrane Labeling with probe Washing to remove unbound probe Detection by autoradiogramAPPLICATIONS : APPLICATIONS A standard for the direct study of gene expression at the level of mRNA (mRNA transcripts) Detection of mRNA transcript size Study RNA degradation Study RNA splicing - can detect alternatively spliced transcripts Study RNA half-life Study IRES (internal ribosomal entry site) – to remove possibility of RNA digestion vs. 2nd cistron translation.Western blotting : Western blotting Discovery??? Dr. Douglas Lake of the University of Arizona School of Medicine's Department of Microbiology and Immunology “A technique in which proteins are separated by gel electrophoresis and transferred to a membrane sheet. A specific protein is then identified through its reaction with a labeled antibody.”Principle: Principle This technique works on the principle on “Antigen-Antibody” relationshipPrerequisite for W.B: Prerequisite for W.B The SDS PAGE technique is a prerequisite for Western blotting. “SDS (sodium dodecyl sulfate) is a detergent (soap) that can dissolve hydrophobic molecules but also has a negative charge (sulfate) attached to it.”Steps in W.B: Steps in W.B 1. Gel electrophoresis: The proteins are separated according to size. 2. Membrane Transfer: Transferring to nitrocellulose by applying current. 3. Blocking: Done to prevent non-specific protein interactions between the membrane and the antibody protein.Blocking in W.B: Blocking in W.B The blot is incubated with a generic protein (such as milk proteins) which binds to any remaining sticky places on the nitrocellulose. An antibody that is specific for the protein of interest(the primary antibody - Ab1) is added to the nitrocellulose sheet and reacts with the antigen. Only the band containing the protein of interest binds the antibody, forming a layer of antibody molecules .Cont..: Cont.. Following several rinses for removal of non-specifically bound Ab1, the Ab1-antigen complex on the nitrocellulose sheet is incubated with a second antibody (Ab2), which recognizes the primary antibody and binds it. Ab2 is radioactively labeled, or is covalently linked to a reporter enzyme, which allows to visualize the protein-Ab1-Ab2 complexApplications : Applications To identify the specific proteins To identify their masses The confirmatory HIV test to detect anti-HIV antibody in a human serum sample. The definitive test for Bovine spongiform encephalopathy (BSE, commonly referred to as ' mad cow disease '). Some forms of Lyme disease testing also employ Western blotting.Protein gel (SDS-PAGE) that has been stained with Coomassie Blue.: Protein gel (SDS-PAGE) that has been stained with Coomassie Blue.Faster Way to Western Blot: Faster Way to Western Blot The Quick Western Kit provides a universal detection reagent that can be combined with the primary antibody incubation step, eliminating the need for a secondary antibody incubation step. This kit works with a variety of primary antibodies. This reduces the overall time to complete a Western blot.PowerPoint Presentation: Standard Western Blot You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.