TAU antibody(Detector)

Synonyms:Microtubule-associated protein tau|Neurofibrillary tangle protein|Paired helical filament-tau (PHF-tau)|MAPT|MAPTL|MTBT1|TAU antibody
Catalogue No.:FNab11183Reactivity:Human
Host:RabbitTested Application:ELISA(Det)
Clonality:MonoclonalIsotype:IgG
Size Price
Dispatch Time: About 3 working days
  • SPECIFICATIONS
  • FIGURES
  • CONDITIONS
  • FAQS
Product Name
TAU antibody(Detector)
Catalogue No.
FNab11183
Size
100μg
Form
liquid
Purification
Protein A affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
Monoclonal
Isotype
IgG
Storage
PBS pH 7.4,-20℃ for 12 months(Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
Synthetic peptide within human Tau aa 57-68.
Alternative Names
Microtubule-associated protein tau|Neurofibrillary tangle protein|Paired helical filament-tau (PHF-tau)|MAPT|MAPTL|MTBT1|TAU antibody
UniProt ID
P10636
Application
Tested Applications
ELISA(Det)
Recommended dilution
Determined by end user
Background
Tau,also known as MAPT (microtubule-associated protein tau),MAPTL,MTBT1 or TAU,is a 758 amino acid protein that localizes to the cytoplasm,as well as to the cytoskeleton and the cell membrane,and contains four Tau/MAP repeats. Expressed in neuronal tissue and existing as multiple alternatively spliced isoforms,Tau functions to promote microtubule assembly and stability and is thought to be involved in the maintenance of neuronal polarity. Tau may also link microtubules with neural plasma membrane components and,addition to its role in microtubule stability,is also necessary for cytoskeletal plasticity. Tau is highly subject to a variety of post-translational modifications,including phosphorylation on serine and threonine residues,polyubiquitination (and subsequent proteasomal degradation) and glycation of specific Tau isoforms. Defects in the gene encoding Tau are associated with Alzheimers disease,pallido-ponto-nigral degeneration (PPND),corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP).
How many times can antibodies be recycled?

First, usually it's not suggested to recycle antibodies. After use, buffer system of antibodies has changed. The storage condition of recycled antibodies for different customers also varies. Thus, the performance efficiency of recycled antibodies can’t be guaranteed. Besides, FineTest ever conducted the antibody recycling assay. Assay results show recycling times of different antibodies also varies. Usually, higher antibody titer allows more repeated use. Customers can determine based on experimental requirements.

Notes: After incubation, we recycle rest antibodies to centrifuge tube and store at 4℃. High titer antibodies can be stored for a minimum of one week. Reuse about three times.

What are components of FineTest antibody buffer?

Components of FineTest antibody buffer are usually PBS with proclin300 or sodium azide, BSA, 50% glycerol. Common preservative is proclin300 or sodium azide, which is widely applied in the lab and industry.

How about the storage temperature and duration of FineTest antibodies?

Most antibodies are stored at -20℃. Directly-labeled flow cytometry antibodies should be stored at 2 - 8℃. The shelf life is one year. If after sales issues for purchased antibodies appear, return or replacement is available. Usually, antibodies can be still used after the one-year warranty. We can offer technical support services.

Is dilution required for FineTest antibodies? What’s the dilute solution?

Directly-labeled flow cytometry antibodies are ready-to-use without dilution. Other antibodies are usually concentrated. Follow the dilution ratio suggested in the manual. Dilute solution for different experiments also varies. Common antibody dilution buffers are acceptable(e.g. PBST, TBST, antibody blocking buffer).

How to retrieve antibodies for immunohistochemistry?

Common retrieval buffers: Tris-EDTA Buffer(pH 9.0); Citrate Buffer(pH 6.0)

Heat induced antibody retrieval:

Method 1: Water-bath heating: Put the beaker with retrieval buffer and slide in the boiling water bath. Keep the boiling state for 15min. Naturally cool to room temperature;

Method 2: Microwave retrieval: Put the beaker with retrieval buffer and slide in the microwave oven. Heat at high power for 5min, Switch OFF for 3min, Heat at medium power for 5min. Naturally cool to room temperature.

How to choose secondary antibodies?

(1) Secondary antibodies react with primary antibodies. Thus, secondary antibodies should be against host species of primary antibodies. E.g. If the primary antibody is derived from rabbit, the relevant secondary antibody should be against rabbit. E.g. goat anti rabbit or donkey anti rabbit.

(2) Choose secondary antibody conjugates according to the experimental type, e.g. ELISA, WB, IHC etc. Common enzyme conjugated secondary antibodies are labelled by HRP, AP etc. Fluorescin or dye labelled secondary antibodies are applied in immunofluorescence and flow cytometry(e.g. FITC, Cy3).

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