Key features and details
- Expression system: Baculovirus infected Sf9 cells
- Purity: > 70% Densitometry
- Active: Yes
- Suitable for: WB, Functional Studies, SDS-PAGE
Product nameRecombinant human STK19/G11 protein
Biological activityThe specific activity of ab139624 was determined to be 2 nmol/min/mg.
Purity> 70 % Densitometry.
Expression systemBaculovirus infected Sf9 cells
Protein lengthFull length protein
SequenceMQKWFSAFDDAIIQRQWRANPSRGGGGVSFTKEVDTNVATGAPPRRQRVP GRACPWREPIRGRRGARPGGGDAGGTPGETVRHCSAPEDPIFRFSSLHSY PFPGTIKSRDMSWKRHHLIPETFGVKRRRKRGPVESDPLRGEPGSARAAV SELMQLFPRGLFEDALPPIVLRSQVYSLVPDRTVADRQLKELQEQGEIRI VQLGFDLDAHGIIFTEDYRTRVLKACDGRPYAGAVQKFLASVLPACGDLS FQQDQMTQTFGFRDSEITHLVNAGVLTVRDAGSWWLAVPGAGRFIKYFVK GRQAVLSMVRKAKYRELLLSELLGRRAPVVVRLGLTYHVHDLIGAQLVDC ISTTSGTLLRLPET
Predicted molecular weight70 kDa including tags
Amino acids1 to 364
Our Abpromise guarantee covers the use of ab139624 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ab204856 (CREB peptide) can be utilized as a substrate for assessing kinase activity
Previously labelled as STK19.
Concentration information loading...
Preparation and Storage
Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Constituents: 0.31% Glutathione, 0.002% PMSF, 0.004% DTT, 0.79% Tris HCl, 0.003% EDTA, 25% Glycerol (glycerin, glycerine), 0.88% Sodium chloride
This product is an active protein and may elicit a biological response in vivo, handle with caution.
RelevanceSTK19 belongs to the serine/threonine protein kinase family. The specific function of this protein is unknown. In vitro it can phosphorylate casein-alpha on serine and threonine residues and histones on serine residues.
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
ab139624 has not yet been referenced specifically in any publications.