WB result of MBP tag Recombinant Rabbit mAb
Primary antibody: MBP tag Recombinant Rabbit mAb at 1/5000 dilution
Lane 1: 293T whole cell lysate 5 µg
Lane 2: 293T transfected with Histone H3-MBP tag whole cell lysate 5 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 43 kDa
Observed MW: 38~60 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Antigen | MBP |
Synonyms | Maltose-binding protein |
Immunogen | Synthetic Peptide |
Accession | P0AEX9 |
Clone Number | S-925-33 |
Antibody Type | Recombinant mAb |
Isotype | IgG |
Application | WB |
Reactivity | Species Independent |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied. |
Dilution
application | dilution | species |
WB | 1:5000 |
Background
Maltose-binding protein (MBP) is a part of the maltose/maltodextrin system of Escherichia coli, which is responsible for the uptake and efficient catabolism of maltodextrins. MBP is used to increase the solubility of recombinant proteins expressed in E. coli. In these systems, the protein of interest is often expressed as a MBP-fusion protein, preventing aggregation of the protein of interest. In addition, MBP can itself be used as an affinity tag for purification of recombinant proteins. The fusion protein binds to amylose columns while all other proteins flow through. The MBP-protein fusion can be purified by eluting the column with maltose. Once the fusion protein is obtained in purified form, the protein of interest is often cleaved from MBP with a specific protease and can then be separated from MBP by affinity chromatography.
Picture
Picture
Western Blot
