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1.
J Biomol Tech ; 14(4): 278-88, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14715886

RESUMO

The Association of Biomolecular Resource Facilities 2003 Edman Sequencing Research Group (ABRF-ESRG'03) sample is the 15th in a series of studies designed to allow participating members to evaluate their abilities to analyze the N-terminus of a protein or peptide using automated Edman degradation chemistry. It is a follow-up study to the ESRG'02 sample, which was a single protein with a heterogeneous N-terminus. Both the 2002 and 2003 samples were obtained from the same protein complex and were resolved by SDS-PAGE followed by electrophoretic transfer to PVDF membrane. The ABRF-ESRG'03 sample had an apparent molecular weight of 49 kDa and a single N-terminus, with initial yields of approximately 2 pmol. Participants were asked to sequence 25 residues and return their results to the ESRG for analysis along with two completed surveys and an area/pmol table for repetitive and initial yield calculations. Data for 46 responses are presented which include initial yields, repetitive yields, sequencer performance, and ability to identify the protein.


Assuntos
Polivinil , Proteínas/química , Sequência de Aminoácidos , Coleta de Dados , Bases de Dados Factuais , Eletroforese em Gel de Poliacrilamida , Ligação Proteica , Proteínas/análise , Proteínas/isolamento & purificação , Análise de Sequência de Proteína
2.
J Biomol Tech ; 13(4): 246-57, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19498990

RESUMO

The ABRF-2002 Edman Sequencing Research Group (ESRG) sample (ABRF-2002ESRG) was the 14th in a yearly series designed as an education and self-evaluation tool for laboratories performing Edman sequence analysis. This year's study used a known protein with a heterogeneous amino-terminus, and thus was one of the more challenging protein samples distributed by an Association for Biomolecular Resource Facilities (ABRF) research group. The sample was originally submitted to an ESRG member's lab, and after analysis was thought to demonstrate an analytical problem that would be of interest to the general sequencing community. The protein was purified using commercially available, pre-cast sodium dodecyl sulfate-polyacrylamide gels and transferred to polyvinylidene fluoride.Protein bands were distributed to 72 members of the ABRF who requested ABRF-2002ESRG, along with a data instruction sheet and a brief survey. Participating members were requested to report observed raw data, interpret the data as they normally would for an investigator, and identify the protein using a database search. Study results from 31 responses are presented to show how labs fared with a difficult but sequenceable sample.

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