ATM ELISA Kit

Produktnummer ABIN1568539

Produktdetails ATM ELISA Kit

Target: ATM (Ataxia Telangiectasia Mutated (ATM))

Reaktivität: Maus

Nachweismethode: Colorimetric

Methodentyp: Sandwich ELISA

Detektionsbereich: 15.625 pg/mL - 1000 pg/mL

Untere Nachweisgrenze: 15.625 pg/mL

Applikation: ELISA

Verwendungszweck: The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of ATM in mouse serum, plasma, tissue homogenates, cell lysates and other biological fluids.

Proben: Cell Lysate, Plasma, Serum, Tissue Homogenate

Analytische Methode: Quantitative

Spezifität: This assay has high sensitivity and excellent specificity for detection of this index.

Kreuzreaktivität (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.

Sensitivität: 5.6 pg/mL

Bestandteile:

• 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

Benötigtes Material:

1. Microplate reader with 450 ± 10nm filter.
2. Precision single or multi-channel pipettes and disposable tips.
3. Eppendorf Tubes for diluting samples.
4. Deionized or distilled water.
5. Absorbent paper for blotting the microtiter plate.
6. Container for Wash Solution.

Anwendungsinformationen

Probenmenge: 100 μL

Testdauer: 1 - 4.5 h

Plattentyp: Pre-coated

Protokoll: 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.

Testdurchführung:

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.

Testpräzision:

• 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%

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Vorsichtsmaßnahmen: The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

Handhabung: 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.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 12 months

Details zu ATM

Target: ATM (Ataxia Telangiectasia Mutated (ATM))

Andere Bezeichnung: ATM (ATM Produkte)

Synonyme: ATM ELISA Kit, Atm ELISA Kit, CG6535 ELISA Kit, Dmel\\CG6535 ELISA Kit, Tefu ELISA Kit, atm ELISA Kit, atm/tefu ELISA Kit, dATM ELISA Kit, tef ELISA Kit, Xatm ELISA Kit, at1 ELISA Kit, atdc ELISA Kit, tel1 ELISA Kit, telo1 ELISA Kit, AT1 ELISA Kit, ATA ELISA Kit, ATC ELISA Kit, ATD ELISA Kit, ATDC ELISA Kit, ATE ELISA Kit, TEL1 ELISA Kit, TELO1 ELISA Kit, AI256621 ELISA Kit, C030026E19Rik ELISA Kit, telomere fusion ELISA Kit, ATM serine/threonine kinase L homeolog ELISA Kit, ATM serine/threonine kinase ELISA Kit, ataxia telangiectasia mutated ELISA Kit, ataxia telangiectasia mutated (atm) ELISA Kit, serine/threonine-protein kinase ATM ELISA Kit, tefu ELISA Kit, atm.L ELISA Kit, atm ELISA Kit, ATM ELISA Kit, EDI_100660 ELISA Kit, CpipJ_CPIJ001772 ELISA Kit, BDBG_08252 ELISA Kit, PAAG_02532 ELISA Kit, MCYG_05088 ELISA Kit, VDBG_06833 ELISA Kit, ACLA_015700 ELISA Kit, LOC5565620 ELISA Kit, MGYG_07634 ELISA Kit, PGTG_14279 ELISA Kit, Atm ELISA Kit

Hintergrund: Alternative name: AT1, ATD, ATA, ATC, ATDC, ATE, TEL1, TELO1, Serine-protein kinase ATM

Gen-ID: 11920

UniProt: Q62388

Pathways: p53 Signalweg, Apoptose, DNA Reparatur, Inositol Metabolic Process, Positive Regulation of Response to DNA Damage Stimulus