Yes, the Cell Signaling Lysis Buffer (43-040) can be used in the Mouse Cytokine Milliplex kit (MCYTOMAG-70K). The buffer was tested at dilutions of 1:2, 1:5, and 1:10 in Assay Buffer, with the 1:5 dilution showing comparable results to the Assay Buffer for most cytokines and the 1:10 dilution providing optimal results if the samples can tolerate that level of dilution.
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Quality Level
species reactivity
mouse
manufacturer/tradename
Milliplex®
assay range
accuracy: 85-107%
standard curve range: 3.2-10,000 pg/mL
technique(s)
multiplexing: suitable
compatibility
configured for Premixed
detection method
fluorometric (Luminex xMAP)
shipped in
wet ice
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This Item | MCYTMAG70PMX25BK | MCYTMAG70PMX32BK | PCYTMG-40K-PX23 |
|---|---|---|---|
| species reactivity mouse | species reactivity mouse | species reactivity mouse | species reactivity nonhuman primates |
| assay range accuracy: 85-107%, standard curve range: 3.2-10,000 pg/mL | assay range - | assay range - | assay range accuracy: 70-101%, linearity: 110.3% |
| 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 |
| compatibility configured for Premixed | compatibility configured for Premixed | compatibility configured for Premixed | compatibility configured for Premixed |
General description
To identify specific cytokines involved in any inflammatory or immune response, it might be necessary to screen panels of cytokines, often requiring some level of automation and/or high throughput. Beads can make the process of automation and high throughput screening easier with features such as walk-away washing. Advantages even outside automation include:
More flexible plate and plate washer options
- Improved performance with turbid serum/plasma samples
- Assay results equivalent to non- beads
- Automated washing avoids many problems associated with vacuum filtration washing
MILLIPLEX® Mouse Cytokine / Chemokine panel enables you to focus on the therapeutic potential of cytokines as well as the modulation of cytokine expression. Coupled with the Luminex® xMAP® platform in a bead format, you receive the advantage of ideal speed and sensitivity, allowing quantitative multiplex detection of dozens of analytes simultaneously, which can dramatically improve productivity.
Panel Type: Cytokines/Chemokines
Application
- Analytes: Eotaxin/CCL11, G-CSF, GM-CSF, IFN-γ, IL-1α, IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-9, IL-10, IL-12 (p40), IL-12 (p70), IL-13, IL-15, IL-17, IP-10, KC, LIF, LIX, MCP-1, M-CSF, MIG, MIP-1α, MIP-1β, MIP-2, RANTES, TNF-α, VEGF
- Recommended Sample type: plasma, serum, or cell culture supernatant
- Recommended Sample dilution: 1:2 diluted plasma or serum
- Assay Run Time: Overnight or one day. For best results an overnight incubation is recommended.
- Research Category: Inflammation & Immunology
Biochem/physiol Actions
Cross-reactivity between the antibodies and any of the other analytes in this panel is non-detectable or negligible.
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Preparation Note
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Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2
Target Organs
Respiratory Tract
Storage Class Code
10 - Combustible liquids
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PRTR
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FSL
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ISHL Indicated Name
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ISHL Notified Names
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Cartagena Act
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Can the Cell Signaling Lysis Buffer (43-040) be used in the Mouse Cytokine Milliplex kit (MCYTOMAG-70K)?
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How do I enter the high, low, and expected concentrations for the kit QCs into Xponent? Since the QC range sheet only includes the high and low ranges, could you please provide the expected concentration as well?
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A quality control range sheet is available, providing different values for quality controls. The expected average per range can be calculated by adding the high and low numbers for each marker, then dividing the total by 2.
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