Recombinant Human OXSR1 protein (ab125579)
Key features and details
- Expression system: Baculovirus infected Sf9 cells
- Purity: > 95% Densitometry
- Suitable for: WB, SDS-PAGE
Description
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Product name
Recombinant Human OXSR1 protein
See all OXSR1 proteins and peptides -
Purity
> 95 % Densitometry.
Purity was determined to be >95% by densitometry. Affinity purified. -
Expression system
Baculovirus infected Sf9 cells -
Accession
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Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
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Species
Human -
Predicted molecular weight
86 kDa including tags -
Amino acids
1 to 527
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Associated products
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Related Products
Specifications
Our Abpromise guarantee covers the use of ab125579 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
Western blot
SDS-PAGE
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Form
Liquid -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
pH: 7.50
Constituents: 0.31% Glutathione, 0.002% PMSF, 0.004% DTT, 0.79% Tris HCl, 0.003% EDTA, 25% Glycerol (glycerin, glycerine), 0.29% Sodium chloride
General Info
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Alternative names
- 2210022N24Rik
- 2810422B09Rik
- AI462649
see all -
Function
Regulates downstream kinases in response to environmental stress. May also have a function in regulating the actin cytoskeleton. -
Tissue specificity
Ubiquitously expressed in all tissue examined. -
Sequence similarities
Belongs to the protein kinase superfamily. STE Ser/Thr protein kinase family. STE20 subfamily.
Contains 1 protein kinase domain. -
Post-translational
modificationsPhosphorylated upon DNA damage, probably by ATM or ATR. - Information by UniProt
Protocols
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.
Datasheets and documents
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SDS download
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Datasheet download
References (0)
ab125579 has not yet been referenced specifically in any publications.