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1 linear when measuring mannose 6-phosphate on electroblots.
2 e detection reagents, following SDS-PAGE and electroblotting.
3 t were then subjected to electrophoresis and electroblotting.
4                             Treatment of the electroblotted allergens with sodium metaperiodate abrog
5 lyacrylamide gel electrophoresis followed by electroblotting and immunochemical staining using monosp
6 ced capture efficiency (on par with membrane electroblotting) and sparing consumption of reagents (ca
7 s without any additional sample preparation, electroblotting, destaining, etc.
8     The amount of mannose 6-phosphate in the electroblots following hydrolysis was determined using H
9  the proteins ErbB2 and bovine serum albumin electroblotted from SDS-PAGE gels onto nitrocellulose.
10 and profiled from individual bands following electroblotting of isoelectric focusing gels.
11  transfer method was developed for efficient electroblotting of proteins separated by acid-urea polya
12                Following electrophoresis and electroblotting of the C5b6 complex to a polyvinylidene
13                                              Electroblotting of the SDS-PAGE and amino acid sequence
14 MALDI-MS analysis of proteins that have been electroblotted onto a nitrocellulose (NC) membrane.
15                                The proteins, electroblotted onto nitrocellulose after SDS--PAGE separ
16 or rapidly cleaving and identifying proteins electroblotted onto poly(vinylidene difluoride) membrane
17 roach using two-dimensional electrophoresis, electroblotting/protein sequencing, high performance liq
18                          With this approach, electroblotted proteins can be analyzed directly for int
19 ganic bases, and 17 detergents to dissociate electroblotted proteins from nitrocellulose.
20 ow reactor for the sequence analysis of PVDF-electroblotted proteins.
21 The protein was labeled with PNBG-[125I]ASA, electroblotted to polyvinylidene difluoride membranes, d
22 d by SDS-polyacrylamide gel electrophoresis, electroblotted to polyvinylidene fluoride membrane, and
23 ee from complexed RNA in agarose, the RNA is electroblotted to positively charged nylon.
24 crylamide gel electrophoresis (SDS-PAGE) and electroblotted to protein-blotting membrane.