Mix & Go! XJb Autolysis Competent Cells
- Fast: 80 - 90% of E.coli are lysed in only 10 minutes after harvesting.
- High Transformation Efficiencies: Achieve 108 - 109 transformants per µg of plasmid DNA.
- Versatile: Fully compatible with a wide range of buffers for protein purification and other physical methods of lysis.
|Autolysis||XJb lysis efficiency is 10-20 % lower than XJa. For optimal lysis, more care needs to be taken when selecting the lysis buffer. However, even very low concentrations of detergent may improve lysis significantly.|
|Cell Growth||A very robust strain, reaching higher OD’s than E. coli K-strains.|
|DNA Extraction||XJb is not optimal for DNA extraction.|
|DNA Stability||This strain is RecA positive.|
|Genotype||F- ompT hsdSB(rB - mB -) gal dcm ΔaraB::ΛR, cat (CmR)|
|Processing Time||10 minutes|
|Product Storage||-70°C to -80°C|
|Protein Expression||XJb is ideal for recombinant protein expression. It lacks Lon and OmpT proteases, leading to higher protein yields.|
|Transformation Efficiency||108 - 109 transformants per µg of plasmid DNA|
Q1: Will chitin be degraded?
Q2: Can glucose be added to the growth media?
Q3: Can glycerol be present during the freeze-thaw cycle?
Q4: What if the lysate is extremely viscous?
Q5: Is a starter culture necessary?
Q6: What buffer should the cell pellet be resuspended in?
Q7: How do you improve lysis efficiency?
Q8: Do heat shock and outgrowth steps have to be performed when transforming XJb Autolysis E. coli?
Q9: Are competent cells GMOs?
Q10: Are the Mix & Go! strains dam+ and dcm+?
Q11: Do the Mix & Go! strains methylate DNA?
Q12: Which strains are equivalent to the Zymo strains?
Q13: How to reduce satellite colonies on agar plates?
Q14: Is it possible to dilute the competent cells?
Q15: Which antibiotics can be used with the Mix & Go! procedure?
Q16: Which Plasmid Size can be used for transformation?
Q17: Which is the recommended DNA concentration and volume for transformation?
Q18: What are some tips to improve transformation efficiency?
Q19: How will a heat-shock affect my Transformation Efficiency?
To clone new GFP-like fluorescent proteins from Obelia medusa, the authors identified the potential genes using expression libraries and cloned the genes into a vector. Expression of the proteins was facilitated by using XJb Autolysis E. coli cells from Zymo Research. The authors were able to purify three proteins from Obelia medusa that fluoresce in three different colors: cyan, green, and yellow.Aglyamova, G.V. et al. (2011) Multi-colored homologs of the green fluorescent protein from hydromedusa Obelia sp. Photochem Photobiol Sci (8):1303-9.
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