MAPT Kit ELISA
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- Antigène Voir toutes MAPT Kits ELISA
- MAPT (Microtubule-Associated Protein tau (MAPT))
- Épitope
- cleaved
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Reactivité
- Humain
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 62.5-4000 pg/mL
- Seuil minimal de détection
- 62.5 pg/mL
- Application
- ELISA
- Fonction
- For the quantitative determination of human cleaved microtubule-associated protein tau (C-MAPT/C-TAU) concentrations in serum, plasma, cerebrospinal fluid (CSF), tissue homogenates, cell lysates.
- Type d'échantillon
- Serum, Plasma, Cerebrospinal Fluid, Tissue Homogenate, Cell Lysate
- Analytical Method
- Quantitative
- Specificité
- This assay has high sensitivity and excellent specificity for detection of human C-MAPT/C-TAU.
- Réactivité croisée (Details)
- Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between the target antigen and all analogues for other species. Therefore, cross reaction may still exist.
- Sensibilité
- 15.6 pg/mL
- Ingrédients
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- Assay plate (12 × 8 coated Microwells)
- Standard (freeze dried)
- Biotin-antibody (100 × concentrate)
- HRP-avidin (100 × concentrate)
- Biotin-antibody Diluent
- HRP-avidin Diluent
- Sample Diluent
- Wash Buffer (25 × concentrate)
- TMB Substrate
- Stop Solution
- Adhesive Strip (for 96 wells)
- Instruction manual
- Featured
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- Indications d'application
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- The supplier is only responsible for the kit itself, but not for the samples consumed during the assay. The user should calculate the possible amount of the samples used in the whole test. Please reserve sufficient samples in advance.
- Samples to be used within 5 days may be stored at 2-8°C, otherwise samples must be stored at -20°C (≤ 1 month) or -80°C (≤ 2 months) to avoid loss of bioactivity and contamination.
- Grossly hemolyzed samples are not suitable for use in this assay.
- If the samples are not indicated in the manual, a preliminary experiment to determine the validity of the kit is necessary.
- Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their particular experiments.
- Tissue or cell extraction samples prepared by chemical lysis buffer may cause unexpected ELISA results due to the impacts of certain chemicals.
- Owing to the possibility of mismatching between antigens from another resource and antibodies used in this supplier's kits (e.g., antibody targets conformational epitope rather than linear epitope), some native or recombinant proteins from other manufacturers may not be recognized by this supplier's products.
- Influenced by factors including cell viability, cell number and cell sampling time, samples from cell culture supernatant may not be recognized by the kit.
- Fresh samples without long time storage are recommended for the test. Otherwise, protein degradation and denaturalization may occur in those samples and finally lead to wrong results.
- Commentaires
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Detection wavelength: 450 nm
Information on standard material:
Depending on the antigen to be detected, standards can be either native or recombinant protein. The recombinant proteins are being expressed in CHO cells in most cases. Please inquire for more information. The formulation of auxiliary material in the standard is considered proprietary information, however it does not contain any poisonous substance. Proclin 300 (1:3000) is used as preservative.
Information on reagents:
In most cases the stop solution provided is 1 N H2SO4. The formulation of wash solution is proprietary information. None of the components contain (sodium) azide, thimerosal, 2-mercaptoethanol (2-ME) or any other poisonous materials. For the sandwich method kits, the sample diluent, antibody diluent, enzyme diluent and standard all contain BSA.
Information on antibodies:
The antibodies provided in different kits vary in regards to clonality and host. Some antibodies are affinity purified, some are Protein A - Volume d'échantillon
- 100 μL
- Durée du test
- 1 - 4.5 h
- Plaque
- Pre-coated
- Protocole
- This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for C-MAPT/C-TAU has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any C-MAPT/C-TAU present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for C-MAPT/C-TAU is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of C-MAPT/C-TAU bound in the initial step. The color development is stopped and the intensity of the color is measured.
- Précision du teste
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Intra-assay precision (precision within an assay): Three samples of known concentration were tested twenty times on one plate to assess precision.
Inter-assay precision (precision between assays): Three samples of known concentration were tested in twenty assays to assess precision.- Intra-assay: CV% less than 8%
- Inter-assay: CV% less than 10%
- Restrictions
- For Research Use only
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- Précaution d'utilisation
- The Stop Solution provided with this kit is an acid solution. Wear eye, hand, face and clothing protection when using this material.
- Conseil sur la manipulation
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- The kit should not be used beyond the expiration date on the kit label.
- Do not mix or substitute reagents with those from other lots or sources.
- If samples generate values higher than the highest standard, dilute the samples with Sample Diluent and repeat the assay.
- Any variation in Sample Diluent, operator, pipetting technique, washing technique, incubation time/temperature and kit age can cause variation in binding.
- This assay is designed to eliminate interference by soluble receptors, binding proteins and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For unopened kit: All the reagents should be kept according to the labels on vials.
- Date de péremption
- 6 months
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A prospective pilot study on serum cleaved tau protein as a neurological marker in severe traumatic brain injury." dans: British journal of neurosurgery, Vol. 31, Issue 3, pp. 356-363, (2018) (PubMed).
: "
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A prospective pilot study on serum cleaved tau protein as a neurological marker in severe traumatic brain injury." dans: British journal of neurosurgery, Vol. 31, Issue 3, pp. 356-363, (2018) (PubMed).
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- Antigène Voir toutes MAPT Kits ELISA
- MAPT (Microtubule-Associated Protein tau (MAPT))
- Abstract
- MAPT Produits
- Synonymes
- DDPAC Kit ELISA, FTDP-17 Kit ELISA, MAPTL Kit ELISA, MSTD Kit ELISA, MTBT1 Kit ELISA, MTBT2 Kit ELISA, PPND Kit ELISA, TAU Kit ELISA, AI413597 Kit ELISA, AW045860 Kit ELISA, Mtapt Kit ELISA, Tau Kit ELISA, RNPTAU Kit ELISA, pTau Kit ELISA, tau Kit ELISA, xtp Kit ELISA, MAPT Kit ELISA, PHF-tau Kit ELISA, slc6a6 Kit ELISA, taut Kit ELISA, wu:fc26e12 Kit ELISA, microtubule associated protein tau Kit ELISA, microtubule-associated protein tau Kit ELISA, microtubule associated protein tau S homeolog Kit ELISA, Microtubule-associated protein tau Kit ELISA, solute carrier family 6 (neurotransmitter transporter), member 6b Kit ELISA, MAPT Kit ELISA, Mapt Kit ELISA, mapt.S Kit ELISA, LOC5580230 Kit ELISA, CpipJ_CPIJ013260 Kit ELISA, tau Kit ELISA, slc6a6b Kit ELISA
- Sujet
- Synonyms: cleaved form of DDPAC, FLJ31424, FTDP-17, MAPTL, MGC138549, MSTD, MTBT1, MTBT2, PPND, TAU, G protein beta1/gamma2 subunit-interacting factor 1|microtubule-associated protein tau, isoform 4
- Pathways
- Signalisation MAPK, Dynamique des Microtubules, M Phase, Regulation of Cell Size
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