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STAT1 ELISA Kit

STAT1 Reaktivität: Human, Maus pTyr701 Colorimetric Sandwich ELISA Cell Lysate, Tissue Lysate
Produktnummer ABIN625244
  • Target Alle STAT1 ELISA Kits anzeigen
    STAT1 (Signal Transducer and Activator of Transcription 1, 91kDa (STAT1))
    Bindungsspezifität
    pTyr701, total
    Reaktivität
    • 12
    • 10
    • 6
    • 1
    Human, Maus
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Applikation
    ELISA
    Verwendungszweck
    Human/Mouse Phospho-Stat 1 (Y701) and Total Stat 1 ELISA Kit. This assay semi-quantitatively measures phophorylated Stat 1 (Tyr701) and Total Stat 1 in lysate samples.
    Proben
    Cell Lysate, Tissue Lysate
    Analytische Methode
    Semi-Quantitative
    Spezifität
    The antibody pair provided in this kit recognizes human and mouse Phospho-Stat1 (pTyr701) + pan Stat1.
    Produktmerkmale
    • Simultaneously measure Phosphorylated protein and pan protein in one experiment (for normalization purpose)
    • Screen numerous different cell lysates without performing a Western Blot analysis
    • Minimal hands-on time, convenient, and non-radioactive material
    Bestandteile
    • Pre-Coated 96-well Strip Microplate
    • Wash Buffer
    • Anti-Phospho Antibody
    • Anti-Pan Antibody
    • HRP-Conjugated Secondary Antibody
    • Streptavidin-Conjugated HRP
    • Assay Diluent
    • TMB One-Step Substrate
    • Stop Solution
    • Lysis Buffer
    • Positive Control Sample
    Benötigtes Material
    • Distilled or deionized water
    • 100 mL and 1 liter graduated cylinders
    • Tubes to prepare sample dilutions
    • Protease and Phosphatase inhibitors
    • Precision pipettes to deliver 2 μL to 1 mL volumes
    • Adjustable 1-25 mL pipettes for reagent preparation
    • Benchtop rocker or shaker
    • Microplate reader capable of measuring absorbance at 450 nm
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  • Probenmenge
    100 μL
    Plattentyp
    Pre-coated
    Protokoll
    1. Prepare all reagents and samples as instructed in the manual.
    2. Add 100 μL of sample or positive control to each well.
    3. Incubate 2.5 h at RT or O/N at 4 °C.
    4. Add 100 μL of prepared primary antibody to each well.
    5. Incubate 1 h at RT.
    6. Add 100 μL of prepared 1X HRP-Streptavidin to each well.
    7. Incubate 1 h at RT.
    8. Add 100 μL of TMB One-Step Substrate Reagent to each well.
    9. Incubate 30 min at RT.
    10. Add 50 μL of Stop Solution to each well.
    11. Read at 450 nm immediately.
    Aufbereitung der Reagenzien
    1. Bring all reagents and samples to room temperature (18 - 25 °C) before use.
      2. Item E, Assay Diluent should be diluted 5-fold with deionized or distilled water before use
      3. Preparation of Positive Control: Briefly spin the Positive Control vial of Item K. Add 700 µL 1x Assay Diluent (Item E, Assay Diluent should be diluted 5-fold with deionized or distilled water before use) into Item K vial to prepare a Positive Control (P-1) Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 6 Solution (See i. Positive Control of part IX.for a typical result in page 10). Dissolve the powder thoroughly by a gentle mix (it can be removed by centrifuge if any precipitate in the solution is found). Pipette 260 µL 1x Assay Diluent into each tube. Use the Positive Control (1) to produce a dilution series (shown below). Mix each tube thoroughly before the next transfer. 1x Assay Diluent serves as the background.
      4. If the Wash Concentrate (20x) (Item B) contains visible crystals, warm to room temperature and mix gently until dissolved. Dilute 20 mL of Wash Buffer Concentrate into deionized or distilled water to yield 400 mL of 1x Wash Buffer.
      5. Briefly spin the biotinylated antibody (Item C) before use. Add 100 µL of 1x Assay Diluent into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4 °C for 5 days or at - 80 °C for one month). The biotinylated Stat1 antibody should be diluted 55-fold with 1x Assay Diuent and used in step 4 of Part VII Assay Procedure. P-1 P-2 P-3 P-4 0 260 µL 260µ l 260 µL Positive Control, Item K vial + 700 µL 1x Assay Diluent Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 7
      6. Briefly spin the HRP-Streptavidin concentrate vial (Item G) and pipette up and down to mix gently before use. HRP-Streptavidin concentrate should be diluted 200-fold with 1x Assay Diluent. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 50 µL of HRP-Streptavidin concentrate into a tube with 10 mL 1x Assay Diluent to prepare a 200-fold diluted HRP-Streptavidin solution (don’t store the diluted solution for next day use). Mix well.
      7. Cell Lysate Buffer should be diluted 2-fold with deionized or distilled water before use (recommend to add protease and phosphatase inhibitors). VII.
    Aufbereitung der Proben

    Cell lysates - Rinse cells with PBS, making sure to remove any remaining PBS before adding the Cell Lysate Buffer. Solubilize cells at 4 x 107 cells/mL in 1x Cell Lysate Buffer (we recommend adding protease and phosphatase inhibitors to Cell Lysate Buffer prior to sample preparation). Pipette up and down to resuspend and incubate the lysates with shaking at 2 - 8° C for 30 minutes. Microcentrifuge at 13,000 rpm for 10 minutes at 2 - 8° C, and transfer the supernates into a clean test tube. Lysates should be used immediately or aliquoted and stored at -70 °C. Avoid repeated Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 5 freeze-thaw cycles. Thawed lysates should be kept on ice prior to use.
    For the initial experiment, we recommend to do a serial dilution testing such as 5-fold and 100-fold dilution for your cell lysates with Assay Diluent (Item E) before use.
    Note: The fold dilution of sample used depends on the abundance of phosphorylated proteins and should be determined empiricallys. More of the sample can be used if signals are too weak. If signals are too strong, the sample can be diluted further.
    Cell Lysate Buffer should be diluted 2-fold with deionized or distilled water before use (recommend to add protease and phosphatase inhibitors).

    Testdurchführung
    1. Bring all reagents to room temperature (18 - 25 °C) before use. It is recommended that all samples or Positive Control should be run at least in duplicate. Add 100 µL of each sample or positive control into appropriate wells (see the following 96 well microplate formate). Cover well with plate holder and incubate for 2.5 hours at room temperature or over night at 4 °C with shaking. 96 well microplate coated with phosphorylated and pan antibodies: Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 8 Anti-Stat1 (Tyr701) Anti-pan Stat1
      2. Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each well with Wash Buffer (300 µL) using a multi-channel pipette or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.
      3. Add 100 µL of prepared 1x biotinylated Stat1 antibody (Reagent Preparation step 5) to each well. Incubate for 1 hour at room temperature with shaking.
      4. Discard the solution. Repeat the wash as in step3.
      5. Add 100 µL of prepared 1X HRP-Streptavidin solution (see Reagent Preparation step 6) to each well. Incubate for 1 hour at room temperature with shaking.
      6. Discard the solution. Repeat the wash as in step3. 1 2 3 4 5 6 7 8 9 10 11 12 A B C D E F G H Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 9
      7. Add 100 µL of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with shaking.
      8. Add 50 µL of Stop Solution (Item I) to each well. Read at 450 nm immediately.
    Ergebnisberechnung

    ELISA data analysis: Average the duplicate readings for each sample or positive control.
    i. Positive Control A431 cells were treated with recombinant human EGF at 37 °C for 20 min. Solubilize cells at 4 x 107 cells/mL in cell lysate buffer. Serial dilutions of lysates were analyzed in this ELISA. Please see step 3 of Part VI. Reagent Preparation for detail. O D = 4 5 0 n m 0.01 0.1 1 10 Assay Diluent Positive control dilution series P-1 P-2 P-3 P-4 0
    ii. Recombinant Human EGF Stimulation of A431 Cell Lines A431 cells were treated or untreated with 100 ng/mL Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 11 recombinant human EGF for 10 min. Cell lysates were analyzed using this phosphoELISA and Western Blot. A). ELISA Anti-Stat 1 (Tyr701) Anti-pan Stat1 O D =4 50 n m 0.0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 hEGF treated A431 Untreated A431 B). Western-Blot Analysis hEGF 10 0 1 0 0 (Min) Anti-phospho-Stat1 Anti-Stat1 (Tyr701) Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 12
    iii. SENSITIVITY The A431 cells were treated with 100 ng/mL recombinant human EGF for 20 minutes to induce phosphorylation of Stat1. Serial dilutions of lysates were analyzed in this ELISA and by Western blot. Immunoblots were incubated with anti-phospho-Stat1 (Tyr701). A). ELISA 20 6.7 2.2 0.74 0.25 0 ( µg ) O D =4 50 n m 0.0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 B). Western-Blot Analysis 50 25 12.5 6.25 3.13 1.56 0.78 0.39 0.2 0 (µg) Phospho-Stat1 (Tyr701) and pan Stat1 ELISA Kit Protocol 13 X

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Handhabung
    Avoid repeated freeze- thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Upon receipt, the kit should be stored at -20 °C. Please use within 6 months from the date of shipment. After initial use, Wash Buffer Concentrate (Item B), Assay Diluent (Item E), TMB One-Step Substrate Reagent (Item H), HRP-Streptavidin (Item G), Stop Solution (Item I) and Cell Lysate Buffer (Item J) should be stored at 4 °C to avoid repeated freeze-thaw cycles. Return unused wells to the pouch containing desiccant pack, reseal along entire edge and store at -20 °C. Reconstituted Positive Control (Item K) should be stored at -70 °C.
    Haltbarkeit
    6 months
  • Target Alle STAT1 ELISA Kits anzeigen
    STAT1 (Signal Transducer and Activator of Transcription 1, 91kDa (STAT1))
    Andere Bezeichnung
    Stat1 (STAT1 Produkte)
    Synonyme
    CANDF7 ELISA Kit, ISGF-3 ELISA Kit, STAT91 ELISA Kit, 2010005J02Rik ELISA Kit, AA408197 ELISA Kit, XStat1 ELISA Kit, STAT4 ELISA Kit, DD6G4-4 ELISA Kit, STAT ELISA Kit, STAT1 ELISA Kit, dZ182H3.3 ELISA Kit, si:by134g18.2 ELISA Kit, si:by51f19.1 ELISA Kit, si:dz182h3.3 ELISA Kit, si:dz199m19.1 ELISA Kit, si:dz73o4.2 ELISA Kit, stat1 ELISA Kit, signal transducer and activator of transcription 1 ELISA Kit, signal transducer and activator of transcription 1 L homeolog ELISA Kit, signal transducer and activator of transcription 1, 91kDa ELISA Kit, signal transducer and activator of transcription 4 ELISA Kit, signal transducer and activator of transcription 1a ELISA Kit, STAT1 ELISA Kit, Stat1 ELISA Kit, stat1.L ELISA Kit, stat4 ELISA Kit, stat1a ELISA Kit
    Hintergrund
    Stat1-Y701
    Gen-ID
    6772
    UniProt
    P42224
    Pathways
    JAK-STAT Signalweg, RTK Signalweg, Interferon-gamma Pathway, Response to Growth Hormone Stimulus, Cellular Response to Molecule of Bacterial Origin, Positive Regulation of Endopeptidase Activity, Hepatitis C, CXCR4-mediated Signaling Events
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