TY - JOUR
T1 - An Improved SDS–Polyacrylamide Gel Electrophoresis for Resolution of Peptides in the Range of 3.5–200KDA
AU - Khalkhali-Ellis, Zhila
N1 - Funding Information:
This work was supported by NIH grant DEO 6891.
PY - 1995
Y1 - 1995
N2 - Resolution of a wide range of polypeptides, 3.5-200kDa, on a single low acrylamide and cross linkage gel of 7.7% T, 2.6% C is described here. Laemmli’s (4) original discontinuous SDS polyacrylamide gel electrophoresis (SDS-PAGE) system is modified by increasing the ionic strength of both stacking and resolving gels, and replacing the usual glycine buffer with a tricine cathode buffer as described by Schagger and von Jagow (7). This system offers the advantage of a wide range of protein fractionation, with sufficient band resolution, on a single, low acrylamide concentration and cross 1inkage gel. Moreover, increased gel ionic concentration allows higher protein and salt load, and renders this system suitable for preparative work.
AB - Resolution of a wide range of polypeptides, 3.5-200kDa, on a single low acrylamide and cross linkage gel of 7.7% T, 2.6% C is described here. Laemmli’s (4) original discontinuous SDS polyacrylamide gel electrophoresis (SDS-PAGE) system is modified by increasing the ionic strength of both stacking and resolving gels, and replacing the usual glycine buffer with a tricine cathode buffer as described by Schagger and von Jagow (7). This system offers the advantage of a wide range of protein fractionation, with sufficient band resolution, on a single, low acrylamide concentration and cross 1inkage gel. Moreover, increased gel ionic concentration allows higher protein and salt load, and renders this system suitable for preparative work.
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U2 - 10.1080/10826069508010103
DO - 10.1080/10826069508010103
M3 - Article
C2 - 7603968
AN - SCOPUS:0029240446
SN - 0032-7484
VL - 25
SP - 1
EP - 9
JO - Preparative Biochemistry
JF - Preparative Biochemistry
IS - 1-2
ER -