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Merck

48-623MAG

MILLIPLEX® Phospho/Total STAT3 Magnetic Bead 2-Plex Kit - Cell Signaling Multiplex Assay

同義詞:

2-Plex Phospho/Total Kit, Cell Signaling STAT3 Kit, STAT3 Bead Kit

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分類程式碼代碼:
12161503
NACRES:
NA.47

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物種活性

human, mouse

品質等級

製造商/商標名

Milliplex®

技術

multiplexing: suitable

檢測方法

fluorometric (Luminex® xMAP® technology)

儲存溫度

2-8°C

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本產品
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

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

detection method

fluorometric (Luminex® xMAP®)

detection method

fluorometric (Luminex xMAP)

detection method

fluorometric (Luminex® xMAP®)

detection method

fluorometric (Luminex® xMAP®)

一般說明

STATs (Signal Transducers and Activators of Transcription) are used by receptors for a wide variety of ligands including cytokines, hormones, growth factors and neurotransmitters. The phosphorylation of STAT proteins at conserved tyrosine residues activates SH2-mediated dimerization followed rapidly by nuclear translocation. STAT dimers bind to IRE (interferon response element) and GAS (gamma interferon-activated sequence) DNA elements, resulting in the transcriptional regulation of downstream genes. STAT pathways play important roles in oncogenesis, tumor progression, angiogenesis, cell motility, immune responses and stem cell differentiation.Protein phosphorylation represents the major mechanism used in regulating cellular functions in all eukaryotic cells. Aberrant phosphorylation has been implicated in the onset and development of many diseases including metabolic disorders, inflammatory disease, cancer, etc. Changes in protein phosphorylation can be attributed to both changes in phosphorylation events as well as changes due to total protein levels. In order to distinguish the changes in phosphorylation from changes in protein expression, it is important to normalize the signal from phosphorylation over the signal from total protein. For this need, the MILLIPLEX® MAP 2-plex Phospho/Total STAT3 Kit (Cat. No. 48-623MAG) has been developed for the simultaneous detection of phosphorylated STAT3 (Tyr705) and total STAT3 in a single well using the Luminex system.

應用

Intracellular Bead-Based Multiplex Assays using the Luminex technology enables the simultaneous relative quantitation of multiple phosphorylation or total pathway proteins in tissue and cell lysate samples. The analytes available for this multiplex kit are: STAT3 (Total), STAT3 (Tyr705).This is an overnight (4°C) incubation assay.This kit must be run using the provided Assay Buffer.This assay requires 25 μL diluted filtered cell lysate per well.The suggested working range of protein concentration for the assay is 1 to 25 μg of total protein/well (25 μL/well at 40 to 1,000 μg/mL).Analytes available:STAT3 (Total)STAT3 (Tyr705)

生化/生理作用

Cross-reactivity between the antibodies and any of the other analytes in this kit is non-detectable or negligible.

包裝

96-well plate

法律資訊

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

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

訊號詞

Danger

危險分類

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

儲存類別代碼

10 - Combustible liquids


分析證明 (COA)

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相關內容

MILLIPLEX®細胞訊號傳導分析儀有助於檢測細胞通路中的磷酸化蛋白和總蛋白。

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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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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