Proteome Analysis Using Gel-LC-MS/MS (Record no. 51969)

MARC details
000 -LEADER
fixed length control field 02138nam a2200229Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625160217.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-17808
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250602s9999 xx |||||s2 |||| ||und|d
245 10 - TITLE STATEMENT
Title Proteome Analysis Using Gel-LC-MS/MS
490 0# - SERIES STATEMENT
Volume/sequential designation Current Protocols in protein Science, 96, p. https://doi.org/10.1002/cpps.93, 2019
520 3# - SUMMARY, ETC.
Summary, etc. This article describes processing of protein samples using 1D SDS gels prior to protease digestion for proteomics workflows that subsequently utilize reversed-phase nanocapillary ultra-high-pressure liquid chromatography (LC)coupled to tandem mass spectrometry (MS/MS). The resulting LC-MS/MS data are used to identify peptides and thereby infer proteins present in samples ranging from simple mixtures to very complex proteomes. Bottom-up proteome studies usually involve quantitative comparisons across several or many samples. For either situation, 1D SDS gels represent a simple, widely available technique that can be used to either fractionate complex proteomes or rapidly clean up low microgram samples with minimal losses. After gel separation and staining/destaining, appropriate gel slices are excised, and in-gel reduction, alkylation, and protease digestion are performed. Digests are then processed for LC-MS/MS analysis. Protocols are described for either sample fractionation with high-throughput processing of many samples or simple cleanup without fractionation. An optional strategy is to conduct in-solution reduction and alkylation prior to running gels, which is advantageous when a large number of samples will be separated into large numbers of fractions. Optimization of trypsin digestion parameters and comparison to in-solution protease digestion are also described.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Goldman, A. R.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Beer, L. A.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Tang, H. Y.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Hembach, P.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Zayas-Bazan, D.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Speicher, D. W.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1IqOjZ90eMUoQNK_q7FqiP1hTxwiLISXl/view?usp=drivesdk">https://drive.google.com/file/d/1IqOjZ90eMUoQNK_q7FqiP1hTxwiLISXl/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
Holdings
Lost status Source of classification or shelving scheme Damaged status Not for loan Collection Home library Current library Shelving location Date acquired Total checkouts Full call number Date last seen Price effective from Koha item type
  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-17808 25.06.2025 25.06.2025 Documentos solicitados