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48-623MAG

MILLIPLEX® Phospho/Total STAT3 Magnetic Bead 2-Plex Kit – Multiplex-Zellsignalisierungsassay

Premixed STAT3 Phospho/Total 2-Plex Cell Signaling Panel

Synonym(e):

2-Plex-Phospho/Total-Kit, Kit für STAT3-Zellsignalisierung, STAT3-Perlen-Kit

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NACRES:
NA.47
UNSPSC Code:
12161503
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Produktname

MILLIPLEX® Phospho/Total STAT3 Magnetic Bead 2-Plex Kit – Multiplex-Zellsignalisierungsassay,

Quality Segment

description

Premixed STAT3 Phospho/Total 2-Plex Cell Signaling Panel

species reactivity

human, mouse

packaging

pkg of 1 ea

manufacturer/tradename

Milliplex®

technique(s)

multiplexing: suitable

input

cell lysate

detection method

fluorometric (Luminex® xMAP® technology)

shipped in

wet ice

storage temp.

2-8°C

General description

This panel targets phosphorylated and total STAT3, a key transcription factor activated by cytokines and growth factors. STAT3 (pY705) is involved in regulating immune response, inflammation, and cell survival. Measuring both phosphorylated and total STAT3 provides insight into pathway activation and protein expression in disease models such as cancer and autoimmune disorders.

Application

MILLIPLEX® Qualified assays undergo rigorous assay development, verification, and Quality Control testing to achieve optimal performance. Simultaneously analyze 2 analytes in human, mouse, or rat cell lysate samples.

Analytes Included: STAT3 (Phospho-Tyr705), STAT3 (Total)

Assay Characteristics: Refer to the assay protocol for details on cross-reactivity, buffer compatibility, lysate control, and recommended loading control (MAPmateControl Assays).

Features and Benefits

  • Simultaneously detect phosphorylated and total STAT3 in a single well
  • Includes STAT3 (Phospho-Tyr705) and STAT3 (Total)
  • Magnetic bead-based format ensures reproducibility and efficient processing
  • Compatible with cell lysates from inflammation, immune response, and cancer studies
  • Ideal for immunology, oncology, and cytokine signaling research
  • Fast, convenient alternative to Western Blotting and immunoprecipitation procedures

Legal Information

Luminex is a registered trademark of Luminex Corp
MAPMATE is a trademark of Merck KGaA, Darmstadt, Germany
MILLIPLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
xMAP is a registered trademark of Luminex Corp

Disclaimer

For research use only. Not for use in diagnostic procedures.

Label License/Sticker for Assay Product:

By opening the packaging containing this Assay Product (which contains fluorescently labeled microsphere beads authorized by Luminex Corporation) or using this Assay Product in any manner, you are consenting and agreeing to be bound by the End User Terms and Conditions and the End User License Agreement available at http://support.diasorin.com/end-user-terms-and-conditions/. If you do not agree to all of the terms and conditions, you must promptly return this Assay Product for a full refund prior to using it in any manner.

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Dieser Artikel
48-610MAG48-625MAG48-622MAG
species reactivity

human, mouse

species reactivity

human

species reactivity

human, rat, mouse

species reactivity

human, rat, mouse

manufacturer/tradename

Milliplex®

manufacturer/tradename

Milliplex®

manufacturer/tradename

Milliplex®

manufacturer/tradename

Milliplex®

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

technique(s)

multiplexing: suitable

technique(s)

multiplexing: suitable

technique(s)

multiplexing: suitable

technique(s)

multiplexing: suitable

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

detection method

fluorometric (Luminex® xMAP® technology)

detection method

fluorometric (Luminex® xMAP® technology)

detection method

fluorometric (Luminex® xMAP® technology)

detection method

fluorometric (Luminex® xMAP® technology)


signalword

Danger

Lagerklasse

10 - Combustible liquids

wgk

WGK 3

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - ED ENV 1 - Eye Dam. 1 - Skin Irrit. 2



Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Verwandter Inhalt

Uncover how cells communicate with MILLIPLEX® cell signaling multiplex assays. Multiplexing with cell signaling phosphoprotein assays based on Luminex® xMAP® technology helps researchers measure phosphoproteins and total proteins within the same or different pathways from a single sample.

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Global Trade Item Number

SKUGTIN
48-623MAG04055977051506

Questions

  1. Do you have a protocol for sample preparation to run PBMCs in the Milliplex Cell Signaling assays?

    1 answer
    1. The protocol for sample preparation in the Milliplex Cell Signaling assays has been developed by the R&D team specifically for a custom assay. It is important to note that this protocol has not been tested in all Cell Signaling panels, so volumes and concentrations may need to be optimized for individual studies.

      Here is a short protocol for PBMC cell lysis:
      1. If PBMC cells are frozen, it is recommended to allow cells to recover for 24 hours in complete media as less than 24 hours of recovery can lead to a decrease in signal.
      2. After 24 hours of recovery, count the cells using an appropriate cell counter.
      3. Pellet the PBMC cells at 1000 x g using a tabletop centrifuge for 5 minutes at room temperature.
      4. Remove the supernatant and wash the cells with PBS.
      5. Pellet the PBMC cells again at 1000 x g using a tabletop centrifuge for 5 minutes at room temperature.
      6. Add 10uL of Lysis Buffer (with 2x concentrated protease inhibitors added just prior to use) per 1-2 million cells.
      7. Gently vortex for 30 seconds before transferring the cell lysate into a centrifuge tube.
      8. Gently rock the cell lysate for 10 minutes at 4°C.
      9. Pellet unbroken cells and organelles at 12,000 x g for 10 minutes at 4°C.
      10. Transfer the clear supernatant into a new centrifuge tube.
      11. It is recommended, at least for the first time, to determine the total protein concentration. If not, then it is recommended to run a lysate titration starting at 10uL sample + 15uL of Assay Buffer 1 and performing a 1:1 serial dilution in Assay Buffer 1.

      For the Custom assay, the optimal total protein concentration was found to be 2 to 6 mg/mL. Additionally, it was determined that 10uL of Lysis Buffer per 1 million PBMC cells yields approximately 2 mg/mL, and adding 10uL of this 2mg/mL sample plus 15uL of Assay Buffer yielded good results. It is advised not to dilute samples in Lysis Buffer; rather, dilute in Assay Buffer 1, which lacks strong detergents. If needed, the amount of Lysis Buffer per PBMC cells can be adjusted, for example, by increasing it to 10uL of Lysis Buffer per 2 million PBMC cells.

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