jagomart
digital resources
picture1_Download Word Excel 2007 11857 | Protein Identification Submission Instructions | Sample Submission


 176x       Filetype DOCX       File size 0.02 MB       Source: www.bioms.pitt.edu


File: Download Word Excel 2007 11857 | Protein Identification Submission Instructions | Sample Submission
protein identification guidelines for sample submission overview of workflow the protein identification service is provided for the analysis of protein samples from gel bands from 1d sds page or gel ...

icon picture DOCX Filetype Word DOCX | Posted on 06 Jul 2022 | 3 years ago
Partial capture of text on file.
                                                                   Protein identification: guidelines for sample submission
                 Overview of workflow
                       The protein identification service is provided for the analysis of protein samples from gel bands from 1D SDS-
                       PAGE or gel spots from 2D-PAGE gels. In-gel reduction alkylation trypsin digestion is applied to samples and the 
                       extracted tryptic peptides are analyzed using liquid chromatography tandem mass spectrometry (LC-MS/MS) 
                       followed by database searching to obtain amino acid sequence.
                               Shevchenko A, Tomas H, Havlis J, Olsen JV, Mann M (2006) “In-gel digestion for mass spectrometric characterization of proteins 
                               and proteomes” Nat Protoc 1(6): 2856-2860. PMID: 17406544
                               Granvogl B, Gruber P, Eichacker LA. (2007) “Standardisation of rapid in-gel digestion by mass spectrometry” Proteomics 7(5): 642-
                               54. PMID: 17340585
                               Granvogl B, Plöscher M, Eichacker LA. (2007) “Sample preparation by in-gel digestion for mass spectrometry-based proteomics” 
                               Anal Bioanal Chem 389(4): 991-1002. PMID: 17639354
                  Examples of applications for protein identification:
                                    Identifying unknown proteins from 1D SDS-PAGE or 2D PAGE gels.
                                    Verification of expression product.
                                    Discovery of interacting partners after immuno-precipitation (IP).
                 Sample preparation
                      Run your 1D or 2D gels. E.g. Tris-Glycine, 4-20%, Bis-Tris 10% MOPS or MES buffer.
                      Recommended amount of protein sample loaded onto the gel: 
                       i.     For a 20kD protein, load 50 ng to 150 ng for identification.
                       ii.    For a 80kD protein, load 200 ng to 0.5ug for identification.
                       iii.   For mixtures of proteins, estimate loading amount so that each gel band has about 1ug of proteins.
                      To reduce contamination of keratins, always wear gloves when handling gels, use dedicated clean glassware, 
                       staining trays for gels and avoid dust which contains human keratin.
                      Stain your gels with Coomassie blue, SYPRO Ruby or “MS friendly” silver stain (please check with 
                       manufacturer’s protocol).
                      Cut out the gel spots/bands using a clean blade; wash between samples to avoid cross-contamination
                                                                                                                     2
                      The gel spots/bands should not be greater than 0.5 cm , about this size “                                                              ” for a 1mm thick gel.
                      Place the samples into a natural colored 1.5mL micro-centrifuge tubes                                                                  (separate tubes for each gel 
                       spot/band) and cover gel pieces with about 50-200µL ddH O. Please do not submit samples in colored tubes.
                                                                                                                           2
                      Clearly label tubes with Ultra-Fine Point permanent Sharpie marker. Label tubes with PI’s initials and number 
                       them consecutively. (Ex: PI-01, PI-02, etc.) 
                 Sample submission
                      Fill out sample submission form http://www.BioMS.pitt.edu/ProteinID_SubmissionForm.pdf
                      Samples with completed submission form can be dropped off at the BST3 (3501 Fifth Ave Pittsburgh, PA 
                       15260).  Please contact the BioMS lab by email bioms@pitt.edu  or lab phone 412-383-5937 // 412 648-1811 to
                       arrange a time for drop off. BioMS Center Lab is on the 9th floor, you will need to stop at the security desk in the
                       lobby and call the lab phone or have the security guard call and one of the lab members will come down to 
                       meet you and pick up the samples.
                      Samples are processed weekly starting on Monday afternoon. Samples received after Monday noon will be 
                       processed the following week.
                                                                                                                                                                                                    Apr-14
            Cost: $80/gel band billed monthly to the 32 digit account code. Please make sure you are registered on the 
             BioMS website in order for us to invoice your lab. 
          Report
          • Results are emailed to investigators on the following Monday with instructions on how to view the data.
                                                                                                                Apr-14
The words contained in this file might help you see if this file matches what you are looking for:

...Protein identification guidelines for sample submission overview of workflow the service is provided analysis samples from gel bands d sds page or spots gels in reduction alkylation trypsin digestion applied to and extracted tryptic peptides are analyzed using liquid chromatography tandem mass spectrometry lc ms followed by database searching obtain amino acid sequence shevchenko a tomas h havlis j olsen jv mann m spectrometric characterization proteins proteomes nat protoc pmid granvogl b gruber p eichacker la standardisation rapid proteomics ploscher preparation based anal bioanal chem examples applications identifying unknown verification expression product discovery interacting partners after immuno precipitation ip run your e g tris glycine bis mops mes buffer recommended amount loaded onto i kd load ng ii ug iii mixtures estimate loading so that each band has about reduce contamination keratins always wear gloves when handling use dedicated clean glassware staining trays avoid du...

no reviews yet
Please Login to review.