Recombinant E. coli KMP11 protein (ab138341)
Key features and details
- Expression system: Escherichia coli
- Purity: > 95% SDS-PAGE
- Tags: His tag N-Terminus
- Suitable for: WB, ELISA, SDS-PAGE, Dot blot
Description
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Product name
Recombinant E. coli KMP11 protein -
Purity
> 95 % SDS-PAGE. -
Expression system
Escherichia coli -
Accession
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Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
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Species
Escherichia coli -
Sequence
MATTYEEFSA KLDRLDQEFN RKMQEQNAKF FADKPDESTL SPEMREHYEK FERMIKEHTE KFNKKMHEHS EHFKQKFAEL LEQQKAAQYP SK -
Predicted molecular weight
19 kDa including tags -
Amino acids
1 to 92 -
Tags
His tag N-Terminus
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Associated products
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Related Products
Specifications
Our Abpromise guarantee covers the use of ab138341 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
ELISA
SDS-PAGE
Dot blot
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Form
Liquid -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
Preservative: 1.7% Imidazole
Constituents: 97% Phosphate Buffer, 0.6% Sodium chloride, 0.1% C13E10
General Info
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Alternative names
- Kinetoplastid membrane protein 11
- Lipophosphoglycan associated protein
- LPGAP
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Relevance
KMP11 may be involved in the regulation of the cytoskeleton through interaction with the subpellicular microtubules. It may be involved in parasite mobility and attachment to the surface of the host cell. It strongly stimulates T-cell proliferation and it is thought to play a role in the immunology of leishmaniasis. -
Cellular localization
Cytoplasm. Note: Associated with microtubules
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)
ab138341 has not yet been referenced specifically in any publications.