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Western blot - FAU antibody (ab43581)

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Product Name
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FAU antibody
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See all FAU antibodies (5)...
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Product type
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Primary antibodies
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Description
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Mouse polyclonal to FAU
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Immunogen
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Recombinant fusion protein containing the full length FAU precursor protein (Human)
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Reacts with
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Hu
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Tested applications
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WB
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Abreviews
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Application notes
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Recommended dilutions WB: 1/1000. Predicted molecular weight: 14 kDa. This is the predicted molecular weight of the unprocessed FAU precursor protein consisting of the ubiquitin-like protein Fubi at the N terminus and ribosomal protein S30 at the C terminus.
Not yet tested in other applications. Optimal dilutions/concentrations should be determined by the end user.
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Research areas
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Cell Biology >> Proteolysis / Ubiquitin >> Proteasome / Ubiquitin >> Ub-like Proteins Chromatin and Nuclear Signaling >> DNA / RNA >> Translation >> Ribosome
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Relevance
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FAU is the cellular homolog of the fox sequence in the Finkel-Biskis-Reilly murine sarcoma virus (FBR-MuSV). It encodes a fusion protein consisting of the ubiquitin-like protein fubi at the N terminus and ribosomal protein S30 at the C terminus. It has been proposed that the fusion protein is post-translationally processed to generate free fubi and free ribosomal protein S30. Fubi is a member of the ubiquitin family, and ribosomal protein S30 belongs to the S30E family of ribosomal proteins. Whereas the function of fubi is currently unknown, ribosomal protein S30 is a component of the 40S subunit of the cytoplasmic ribosome. Pseudogenes derived from this gene are present in the genome. Similar to ribosomal protein S30, ribosomal proteins S27a and L40 are synthesized as fusion proteins with ubiquitin.
This antibody was raised by a genetic immunization technique. Genetic immunization can be used to generate antibodies by directly delivering antigen-coding DNA into the animal, rather than injecting a protein or peptide (Tang et al. PubMed: 1545867; Chambers and Johnston PubMed 12910245; Barry and Johnston PubMed: 9234514). The animal's cells produce the protein, which stimulates the animal's immune system to produce antibodies against that particular protein. A vector coding for a partial fusion protein was used for genetic immunisation of a mouse and the resulting serum was tested in Western blot against an E.coli lysate containing that partial fusion protein. Genetic immunization offers enormous advantages over the traditional protein-based immunization method. DNA is faster, cheaper and easier to produce and can be produced by standard techniques readily amenable to automation. Furthermore, the antibodies generated by genetic immunization are usually of superior quality with regard to specificity, affinity and recognizing the native protein.
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Database links
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The links below go to external sites and will open in a new browser window
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Raised in
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Mouse
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Clonality
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Polyclonal
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Isotype
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IgG
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Purity
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Whole antiserum
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Storage buffer
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Preservative: None Constituents: 50% Glycerol, Whole serum Material safety datasheet (MSDS) for this product: Glycerol MSDS
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Form
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Liquid
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Concentration
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Concentration not determined - why is this?
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Storage instructions
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Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
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At Abcam, we have one centralized database to hold all of our product information, so that everything we know about this FAU antibody is on this datasheet. But please do contact us if you would like any reassurance! |
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See below for FAU antibody images, references, products related to ab43581 and other tools.
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FAU antibody images:
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Western blot - FAU antibody (ab43581)
All lanes : FAU antibody (ab43581) at 1/1000 dilution
Lane 1 : Total protein extract from E.coli with ~50ng to 100ng of a negative control fusion protein with an irrelevant antigen Lane 2 : Total protein extract from E.coli with ~50ng to 500ng of the antigen fusion protein
Secondary Rabbit anti-mouse IgG + IgM, (H+L) horseradish peroxidase conjugated at 1/5000 dilution developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 14 kDa
The predicted molecular weight is the molecular weight of the unprocessed FAU precursor protein consisting of the ubiquitin-like protein Fubi at the N terminus and ribosomal protein S30 at the C terminus.
The size of the protein band was not determined. The molecular weight of the band on the western blot does not correspond to the predicted molecular weight of the natural protein because of the additional mass of the fusion.
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Search PubMed (MEDLINE) for references to FAU
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FAU antibody - more information
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Customer reviews (feedback) regarding FAU antibody |
Customer FAQs regarding FAU antibody |
Protocols for FAU antibody |
Price and availability of products related to FAU antibody |
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FAU antibody - related products:
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FAU antibody - other tools:
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Contact Abcam with a Technical Enquiry about FAU antibody |
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All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"