E2F1 Kit ELISA
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- Antigène Voir toutes E2F1 Kits ELISA
- E2F1 (E2F Transcription Factor 1 (E2F1))
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Reactivité
- Humain
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 0.156 ng/mL - 10 ng/mL
- Seuil minimal de détection
- 0.156 ng/mL
- Application
- ELISA
- Fonction
- The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of E2F1 in human tissue homogenates and other biological fluids.
- Type d'échantillon
- Tissue Homogenate
- Analytical Method
- Quantitative
- Specificité
- This assay has high sensitivity and excellent specificity for detection of this index.
- Réactivité croisée (Details)
- No significant cross-reactivity or interference between this index and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between this index and all the analogues, therefore, cross reaction may still exist.
- Sensibilité
- 0.054 ng/mL
- Ingrédients
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- Pre-coated, ready to use 96-well strip plate
- Standard (freeze dried)
- Standard Diluent
- Detection Reagent A
- Detection Reagent B
- Assay Diluent A
- Assay Diluent B
- TMB
- Stop Solution
- Wash Buffer (30X)
- Plate sealer for 96 wells
- Instruction manual
- Matériel non inclus
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- Microplate reader with 450 ± 10nm filter.
- Precision single or multi-channel pipettes and disposable tips.
- Eppendorf Tubes for diluting samples.
- Deionized or distilled water.
- Absorbent paper for blotting the microtiter plate.
- Container for Wash Solution.
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- Volume d'échantillon
- 100 μL
- Durée du test
- 1 - 4.5 h
- Plaque
- Pre-coated
- Protocole
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1. Prepare all reagents, samples and standards
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37°C
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C
4. Aspirate and wash 3 times
5. Add 100µL prepared Detection Reagent B. Incubate 1 hour at 37°C
6. Aspirate and wash 5 times
7. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37°C
8. Add 50µL Stop Solution. Read at 450nm immediately. - Procédure de l'essai
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The microtiter plate provided in this kit has been pre-coated with an antibody specific to the index. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to the index. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain the index, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of the index in the samples is then determined by comparing the O.D. of the samples to the standard curve.
- Précision du teste
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- Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level the index were tested 20 times on one plate, respectively.
- Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level the index were tested on 3 different plates, 8 replicates in each plate.
- CV(%) = SD/meanX100
- Intra-assay: CV<10%
- Inter-assay: CV<12%
- Restrictions
- For Research Use only
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- Précaution d'utilisation
- The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
- Conseil sur la manipulation
- The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage conditions. Note: To minimize unnecessary influences on the performance, operation procedures and lab conditions, especially room temperature, air humidity and incubator temperatures should be strictly regulated. It is also strongly suggested that the whole assay is performed by the same experimenter from the beginning to the end.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- The Assay Plate, Standard, Detection Reagent A and Detection Reagent B should be stored at -20°C upon being received. After receiving the kit , Substrate should be always stored at 4°C.Other reagents are kept according to the labels on vials. But for long term storage, please keep the whole kit at -20°C. The unused strips should be kept in a sealed bag with the desiccant provided to minimize exposure to damp air. The test kit may be used throughout the expiration date of the kit (six months from the date of manufacture). Opened test kits will remain stable until the expiring date shown, provided it is stored as prescribed above.
- Date de péremption
- 12 months
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- Antigène Voir toutes E2F1 Kits ELISA
- E2F1 (E2F Transcription Factor 1 (E2F1))
- Autre désignation
- E2F1 (E2F1 Produits)
- Synonymes
- CG6376 Kit ELISA, DRTF1/E2F Kit ELISA, DmE2F-1 Kit ELISA, Dmel\\CG6376 Kit ELISA, Dp Kit ELISA, E(Sev-CycE)3A Kit ELISA, E(var)3-93E Kit ELISA, E(var)3-95E Kit ELISA, E(var)93E Kit ELISA, E2F Kit ELISA, E2F-1 Kit ELISA, E2F1 Kit ELISA, E2f1 Kit ELISA, Evar(3)164 Kit ELISA, dE2F Kit ELISA, dE2F1 Kit ELISA, dE2f Kit ELISA, dE2f1 Kit ELISA, de2f1 Kit ELISA, def21 Kit ELISA, drosE2F1 Kit ELISA, e2f Kit ELISA, e2f1 Kit ELISA, l(3)07172 Kit ELISA, l(3)j3B1 Kit ELISA, l(3)j3C2 Kit ELISA, l(3)rM729 Kit ELISA, RBAP1 Kit ELISA, RBBP3 Kit ELISA, RBP3 Kit ELISA, mKIAA4009 Kit ELISA, xE2F Kit ELISA, ATE2FB Kit ELISA, E2F TRANSCRIPTION FACTOR-1 E2F1 Kit ELISA, E2F transcription factor 1 Kit ELISA, E2FB Kit ELISA, E2FB TRANSCRIPTION FACTOR Kit ELISA, E2F transcription factor 1 Kit ELISA, E2F transcription factor 1 L homeolog Kit ELISA, E2f1 Kit ELISA, E2F1 Kit ELISA, e2f1.L Kit ELISA
- Sujet
- Alternative name: RBBP3, RBP3, RBAP-1, Retinoblastoma-associated protein 1, Retinoblastoma-binding protein 3, pRB-binding protein E2F-1
- ID gène
- 1869
- UniProt
- Q01094
- Pathways
- Signalisation p53, Cycle Cellulaire, Mitotic G1-G1/S Phases, DNA Replication, M Phase, Autophagy
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