BBa_J70620

BBa_J70620 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_J70620
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Joseph Lynch
Date created: 2010-08-04 11:00:00
Date modified: 2015-05-08 01:08:25

RFC12 Maltose Binding Protein Internal Domain [malE]



Types
DnaRegion

Roles
tag

Tag

Sequences BBa_J70620_sequence (Version 1)

Description

This Maltose-binding protein is designed for either N-terminal or C-terminal fusions. MBP fused proteins can be purified in one step affinity chromatography using a cross-linked amylose matrix and then eluted with 10 mM maltose. Note that the amylose matrix can only be regenerated, in most cases, up to five times. The large size of this tag can also affect the fused protein.

MBP fusions often have higher levels of expression and solubility that the native untagged protein, with typical yields of up to 40 mg/liter culture.

Notes

Primers:

Source

pMAL-c2x

Sequence Annotation Location Component / Role(s)
MBP
Asparagine Spacer
1,1093
1094,1138
feature/cds CDS
tag feature/tag
igem#sampleStatus
Not in stock
igem#status
Unavailable
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_J70620/1