Recombinant Dog Interferon alpha 1 protein (ab169720)
Key features and details
- Expression system: Yeast
- Purity: > 95% Ion Exchange Chromatography
- Suitable for: SDS-PAGE
Description
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Product name
Recombinant Dog Interferon alpha 1 protein
See all Interferon alpha 1 proteins and peptides -
Purity
> 95 % Ion Exchange Chromatography.
Purity: >95% as visualized by SDS-PAGE analysis. -
Expression system
Yeast -
Accession
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Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
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Species
Dog -
Sequence
CHLPDTHGLR NWRVLTLLGQ MRRLSAGSCD HYTNDFAFPK ELFDGQRLQE AQALSVVHVM TQKVFHLFCP DTSSAPWNMT LLEELCSGLS EQLDDLEACP LQEAGLAETP LMHEDSTLRT YFQRISLYLQ DRNHSPCAWE MVRAEIGRSF FSSTILQERI RRRK -
Predicted molecular weight
19 kDa -
Amino acids
24 to 187 -
Additional sequence information
Mature protein without signal peptide.
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Specifications
Our Abpromise guarantee covers the use of ab169720 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
SDS-PAGE
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Form
Lyophilized -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped at 4°C. Store at -20°C.
Constituents: 90% PBS, 10% Trehalose
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ReconstitutionReconstitute with sterile phosphate-buffered saline containing at least 0.1% carrier protein. Store in working aliquots at -20°C. Avoid repeated freeze/thaw cycles.
General Info
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Alternative names
- IFL
- IFN
- IFN alpha
see all -
Function
Produced by macrophages, IFN-alpha have antiviral activities. Interferon stimulates the production of two enzymes: a protein kinase and an oligoadenylate synthetase. -
Sequence similarities
Belongs to the alpha/beta interferon family. -
Cellular localization
Secreted. - 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
References (0)
ab169720 has not yet been referenced specifically in any publications.